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Molecular basis of acute coronary syndrome
Natalya Balashkevich1, Maxut Kazymov2, Marat Syzdykbayev3, Aima Adylova4
1 Department of Medical Education, Semey Medical University, Semey, Kazakhstan
2 Department of Family Medicine, Semey Medical University, Semey, Kazakhstan
3 Department of Anesthesiology, Reanimatology and Narcology, Semey Medical University, Semey, Kazakhstan
4 Department of Public Health, Kazakhstan School of Public Health, Almaty, Kazakhstan
| Date of Submission | 06-Aug-2021 |
| Date of Decision | 08-Dec-2021 |
| Date of Acceptance | 24-Jan-2022 |
| Date of Web Publication | 30-May-2022 |
Correspondence Address:
Dr. Aima Adylova
Kazakhstan School of Public Health, Almaty
Kazakhstan
 Source of Support: None, Conflict of Interest: None  | Check |
DOI: 10.4103/jrms.jrms_695_21
Cardiovascular diseases (CVD) comprise of various heart and blood vessels-related diseases. Acute coronary syndrome (ACS) is one of them. Basic researchers and cardiologists have witnessed landmark developments related to ACS and despite rapid refinement in our understanding; scientists are seeking answers for more questions. Scientists have mapped wide ranging proteins and intricate protein networks which play central role in the pathogenesis in ACS. In this review, we have attempted to summarize underlying causes of ACS. Better understanding of the disease pathology will enable us to get a step closer to an effective clinical management.
Keywords: Acute coronary syndrome, signaling, therapy
How to cite this article:
Balashkevich N, Kazymov M, Syzdykbayev M, Adylova A. Molecular basis of acute coronary syndrome. J Res Med Sci 2022;27:40 |
| Introduction | |  |
Cardiovascular diseases (CVD) comprise of various heart and blood vessels-related diseases. Acute coronary syndrome (ACS) is one of them. Coronary artery disease (CAD), coronary heart disease (CHD), and ACS are the terms which most researchers still use interchangeably. However, the molecular biology of all these diseases is quite different. ACS is said to be a subclass of the CAD, and in the same context, CHD occurs because of the CAD. CAD may be asymptomatic; however, ACS always occurs with visible symptoms.[1] CAD occurs with the blockage of the coronary arteries with atherosclerotic plaque accumulation. As a result, the blood and oxygen flow towards heart decreases. When this condition worsens up, then it can cause unstable angina (UA) along with the myocardial infarction. It includes the ST-elevation myocardial infarction (STEMI) which the health professionals also refer to as Q-wave myocardial infarction. The other condition which can co-occur with the UA is the non-STEMI also known as non-Q-wave myocardial infarction. These conditions cause a massive blockage of blood and oxygen flow toward the heart which makes it a lethal disease among native Americans.[2]
Nausea, chest pain, dyspnea, muscular pain, lightheadedness, referred pain, vomiting, and diaphoresis are some of the symptoms present in patients suffering from ACS. Not all these symptoms necessarily present in the patient with ACS. Almost 4%–14% of these patients have the severe pain and the pain may be present in one arm both arms. The jaw, neck, shoulders, and backbone may also feel the pain and sometime the pain in this situation feel like radiating or travelling from chest to the arm and to the other arm.[3],[4] Inflammation and has quite decisive role in the occurrence of the heart disease especially heart failure. Numerous inflammatory mediators have central roles in the development of heart-related inflammatory diseases. Whenever the accumulation of cholesterol in the vessel walls surpasses the levels kept under control by macrophages, cholesterol precipitates into cholesterol crystals. However, extensive research is required to study the exact cause and link between inflammation and these heart diseases such as ACS.[5]
Low levels of 25 (OH) D have been reported to be associated with prevalent CADs[6].
An important study emphasized on the necessity of giving more attention to psychological factors in primary prevention levels with reference to the public welfare and quality of life of patients with CHD.[7] More importantly, acute stress, depression, hostility, and vital exhaustion have been interconnected with rise in the levels of pro-inflammatory cytokines. Therefore, psychological interventions are advantageous mainly in context of ACS patients.[8]
There are some good reviews related to underlying mechanisms of ACS.[9],[10],[11],[12],[13],[14],[15] In this review, we have summarized most intriguing seminal research works which refined our understanding about the pathogenesis of ACS.
| Involvement of NLRP3 | | |
NLRP3 inflammasome is one of the most widely known NLR complex which are known to have role in CVD because of their critical involvement in innate immunity.[16],[17] NLRP3 encodes for three domains which are NOD, LRR, and the Pyrin domain containing protein 3. The LRR domain further encodes the leucine rich repeat domain and forms the carboxyl terminal of the NLRP3 domain.[18] Countless researchers have described the crucial role of NLRP3 in various autoinflammatory diseases and its relationship with the IL-1 in case of inflammatory diseases.[19],[20] Signals like stimulation of the cytokines and the activation of TLRs can induce and stimulate the NLRP3. The NLRP3 gene consists of the pyrin domains which constitutes the amino terminal of its expressed protein, a binding domain for the nucleotide in the central region and the LRR domain at the C-terminal of its expressed protein.[21] The LRR domain in NLRP3 aids in detecting any unusual and dangerous signals and then the whole gene acts accordingly.
Atherosclerosis is an inflammatory disease contributing towards ACS. It occurs due to the inequity between the mediators and inhibitors of the inflammatory system. This instability between the stimulatory mediators and the inhibitors results in the atherosclerotic plaque build-up in the arterial walls. Interleukin (IL-27) is a known cytokine with immunomodulatory properties in case of inflammatory diseases. The over expression of IL-27 can cause an increase in the atherosclerotic plaque buildup which leads to atherosclerosis. Moreover, patients with ACS and myocardial infarction have elevated levels of the IL-27 in their bloodstream.[22] NLRP3 inflammasome along with some other immune cells has proven key roles in stimulating the atherosclerosis inflammation. Any person having the atherosclerosis inflammation has cholesterol crystals and these crystals play a vital role in the activation of NLRP3 inflammasome and it furthers results in the activation of the IL-18 and IL-1 β which causes atherosclerosis [Figure 1].[23] Phagocytosis of cholesterol crystals causes lysosomal damage which is sensed by NLRP3 inflammasomes, resulting in the release of IL-1 β.[23] Expression levels of IL-1 β have been reported to be upregulated in atherosclerotic pathologies and connected to severity of the disease. In accordance with this approach, to target the downstream effectors of NLRP3 inflammasome, different pharmacological agents have been shown to be effective. Canakinumab, a monoclonal antibody (mAb) against IL-1 β significantly reduced risk of recurrent cardiovascular processes thus highlighting a critical role of IL-1 β in atherosclerotic pathologies. Incubation of the carotid plaques with cholesterol crystals led to higher amounts of IL-1 β. More interestingly, complement-activated product (C5a), displayed effective biological activities that resulted in inflammatory sequelae. Priming with C5a before incubation with cholesterol crystals considerably increased the release of IL-1 β and IL-18. Similarly, priming with the combinatorial treatment (C5a and tumor node factor) before stimulation with cholesterol crystals activated inflammation through induction of NLRP3-transcriptional networks in the plaques.[23] | Figure 1: Plasma low-density lipoproteins (LDL) enter through the arterial wall. LDLs accumulate in mononuclear phagocytes through scavenger receptors. Later, lipid-laden macrophage foam cells die. Death of lipid-rich macrophage foam cells resulted in the accumulation of extracellular cholesteryl ester and cholesterol monohydrate crystals in the lipid-enriched necrotic cores of the plaque. Cholesterol crystals can trigger the activation of the inflammasome that generates biologically active version of the proinflammatory cytokines Interleukin-1 β (IL-1) and IL-18
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Inflammasome complex comprises of various inflammatory proteins which have a crucial part in innate immunity against infections and pathogen invading. However, abnormal upregulation of these inflammatory proteins can cause serious inflammatory and autoimmune disorders. These diseases include numerous heart-related diseases and blood clotting disorders such as thrombosis. NLRP3 inflammasome is the only inflammasome which creates a strong relationship between inflammation and thrombosis. The activation of the NLRP3 inflammasome gives rise to the maturation of the IL-18 and IL-1 β cytokines which fight against invading pathogens as part of innate immunity, but their upregulated expression gives rise to the inflammasome mediators which have a key role in thrombosis and atherosclerosis leading to ACS.[24],[25]
These ILs have proven roles in aiding the inflammatory cascade and plague progression.[26] An important study conducted on patients having ACS provided interesting findings. As NLRP3 has a proven role in the atherosclerosis which leads to ACS so in this research rosuvastatin drug was given to the patients in optimized doses. This drug downregulated the expression of the NLRP3 and its other mediators thus relieving in atherosclerosis inflammation. At a concentration of 20 mg, Rosuvastatin significantly decreased the levels of NLRP3, cathepsin-B, and their downstream cytokines.[27]
Many researchers have proved that colchicine can also target the NLRP3 receptors and downregulate its expression and inflammation because of its anti-inflammatory properties especially in case of ACS.[28] ACS patients demonstrated significantly higher levels of CCL2 and CX3CL1. Colchicine use in ACS and CAD patients has been supported by findings from the LoDoCo trial and COLPLAST-ACS study.[19] As IL-18 and IL-1 β are the known cytokine inflammatory mediators induced by NLRP3, so researchers have used colchicine in order to block the NLRP3 inflammation cascade to prevent ACS and various other inflammatory diseases.[29],[30] Statin drug is known to have therapeutic effects in case of hyperlipidemia and numerous hear-related diseases. Its anti-inflammatory and immunomodulatory properties have made it useful to use it against CVD. Several studies have shown its properties to target the NLRP3 inflammasome and various other downstream inflammatory mediators. The use of statin in patient with inflammatory diseases such as atherosclerosis can provide a relief by targeting the inflammatory mediators like NLRP3 which give rise to atherosclerosis.[31]
ACS comes with several complications and coronary microembolization (CME) is one of them which cause the myocardial infarction. When the NLRP3 inflammasome gets activated in ACS after the CME, then it stimulates the TLR4/MyD88/NF-&# 954;B signaling pathway which has central role in the myocardial inflammation after other inflammatory mediators. This signaling pathway has stimulating role toward the NLRP3 inflammation and ultimately gives rise to the inflammatory cascade in ACS. In order to inhibit the inflammatory mediators and NLRP3 inflammasome, inhibition of TLR4/MyD88/NF-κB is required. Inhibition of the TLR4/MyD88/NF-κB signaling pathway results in the reduction of the NLRP3 inflammasome and its mediators' release and helps to improve the cardiac condition in case of CME and ACS.[32] Several studies and case studies have been conducted to evaluate the nature of relationship between NLRP3 and ACS. In a recent study, case study was conducted including the normal individuals, patients with stable angina pectoris (SAP) and patients having ACS. In all these individuals the level of the platelet NLRP3 was evaluated using various molecular techniques. Individuals with ACS clearly represented higher levels of NLRP3 than those of the SAP patients and normal individuals which leads to the clear deduction that platelet NLRP3 co-occurs with the ACS.[33] A similar study was done to evaluate the correlation between severity of coronary atherosclerosis in patients with ACS with the level of NLRP3 inflammasome. When the follow-up of the individuals was taken for major adverse cardiac events, it clearly represented elevated levels of NLRP3 inflammasome in ACS patients. The results depicted that the levels of NLRP3 inflammasome increased with the severity of the coronary atherosclerosis.[34] Ticagrelor is known to have promising antiplatelet properties but recently its inhibiting properties for NLRP3 inflammasome has been discovered in patients with ACS. It has the ability to suppress the overexpressing NLRP3 inflammasome in macrophages which leads toward several dangerous inflammatory diseases including ACS independent of its novel role in P2Y12 signaling pathway. Ticagrelor has also been approved by FDA as a therapeutic agent in the treatment of CAD.[35]
| Involvement of Different Signaling Pathways in Acute Coronary Syndrome | | |
Reduction in the levels of miR-224 or hyperactivation of Transforming growth factor/Small body size Mothers Against Decapentaplegic (TGFβ/SMAD) cascade increased the intima surface and area of atherosclerotic plaques in thoracic aorta in rat with myocardial infarction.[36]
1% cholesterol diet increased miR-155 expression while conjugated linoleic acid blend supplementation led to downregulation of miR-155 expression in the aorta during atherosclerosis regression in vivo. miR-155 mimics effectively reduced anti-inflammatory proteins, BCL6, and p-STAT-3 in macrophages.[37]
miR-19b inhibited unstable plaque formation by the negative regulation of endothelial cell proliferation, migration, and angiogenesis. miR-19b exerted inhibitory effects on vulnerable plaque formation by inhibition of STAT3 signaling.[38]
IL-9 expression was higher in aortic arches in ApoE−/− mice fed with western diets.[39] Aortic plaque burden was noted to be reduced significantly in mice treated with IL-9 mAbs. Moreover, the size of the plaques in the aortic roots was reduced in experimental rodent models after treatment with IL-9 mAbs. Furthermore, IL-9 mAbs considerably reduced the infiltration areas of macrophage and CD3+ T cells in plaques. Interestingly, IL-9 induced VCAM-1 expression in murine aortic endothelial cells through STAT3-mediated cascade. VCAM-1 neutralization prevented IL-9-mediated increase in the size of plaques.[39]
Importantly, there was a significantly greater subpopulation of IL-17+ FOXP3+ T cells noted in the patients of ACS. Importantly, IL-17+ FOXP3+ cells are “inflammatory” Treg cells reported in the pathological microenvironment which fueled inflammatory activities in patients of ACS. Study provided proof of significant binding of STAT5 to the FOXP3 locus in STAT3-silenced cells. STAT5 overexpression led to an increase in the number of Treg cells but a decreased number of Th17 cells in ACS patients. STAT3 inhibition substantially suppressed the proportions of IL-17-producing cells but upregulated the expression of FOXP3 and enhanced the functions of Treg cells.[40]
| Involvement of Noncoding RNAs | | |
Noncoding RNAs have been widely associated with the regulation of gene expression in various contexts, including virtually all the aspects of development and pathogenesis.[41],[42],[43],[44],[45],[46],[47],[48] In this section, we contextualize and discuss the emerging principles that define how noncoding RNAs play contributory role in ACS.
Circulating miR-221/222 levels in ACS patients have been reported to be elevated and positively correlated with the severity of the coronary artery lesions.[49]
Increase in the plasma levels of miR-146a-5p and miR-21-5p can be considered as circulating biomarkers for ACS patients.[50] Serum exosomal miR-146a has also been reported to hold potential as a novel diagnostic biomarker for ACS patients.[51]
miR-3646 knockdown has been shown to alleviate ACS by reversal of inflammatory responses.[52]
T-lymphocytes played critical roles in the progression of atherosclerosis, and inflammatory cytokines secreted by CD4+ T-cells directly stabilized atherosclerotic plaques through activation of macrophages, thus leading to ACS. miR-let-7i overexpression suppressed apoptotic death in CD4+ T-cells and improved the survival rate of the cells, whereas inhibition of miR-let-7i led to an increase in cell apoptosis. It was found that miR-let-7i directly targeted FasL and Fas in CD4+ T-cells.[53]
miR-378c protected against atherosclerosis by direct inhibition of Sterile Alpha motif domain containing-1 (SAMD1).[54] miR-378c downregulation results in an increase in the VSMCs phenotypic modulation, which is a critical step in atherosclerosis. Importantly, phenotypic transition of VSMCs from the differentiated to de-differentiated state is accompanied by cellular proliferation and migration, which are the hallmark features of atherosclerosis. SAMD1 is a newly reported low-density lipoprotein (LDL)-binding protein. Binding of LDLs with SAMD1 on the cell surface promoted LDL oxidation and subsequent formation of the foam cells.[54]
Blood lipid levels and inflammatory contents were found to be reduced in ACS model of the rodents treated with miR-335-5p agomirs.[55] miR-335-5p overexpression effectively reduced lesion areas, consequently leading to a marked reduction in atherosclerosis in ACS mice. In addition, miR-335-5p upregulation reduced the lipid accumulation, hence causing a suppression of formation of the plaques.[55]
Based on the data provided by the World Health Organization, ACS is the leading cause of fatalities world widely. Because of the unexpected onset and speedy development, it is much needed to stop this disease at its early stages. Previously, various biomarkers used for the diagnosis of ACS include glycosylated hemoglobin (HbA1c)[56]), Cardiac troponin T (cTnT), Cardiac troponin I (cTnI),[57] phospholipid protein,[58] myoglobin, cTnI/cTnT (particularly the hypersensitive troponin I/T), B-type natriuretic peptide,[59] creatine kinase-MB, and gremlin 1, and macrophage migration inhibitory factor.[60] However, the limitation of these markers is that some of these also have elevated levels in other diseases than ACS. Human genome has more than 90% part specified to the noncoding RNAs (ncRNAs). This noncoding RNAs as the name shows they don't code for any protein, so they are considered as part of the genetic junk. Because of the abundant availability and their specialized effects upon the gene regulation at the posttranscriptional level and also because of their crucial role in the development of different diseases, they can be used as promising diagnostic markers for early detection of numerous diseases, especially CVDs.[61] These ncRNAs include micro RNAs (miRNA or miR), circular RNAs, and long noncoding RNAs. All these ncRNAs have a vital role in regulating the expression of genes as well as in the development of cardiac diseases.[62] Various studies have also reported the significant role of these ncRNAs in the early diagnosis of various CVD.[63]
In an important study, the role of circulatory miR-92a in patients having type 2 diabetes mellitus (T2DM) along with the ACS in CHD was evaluated. Two groups of individuals were included in this study. One is the DACS (patients having ACS along with the history of T2DM), CACS (patients having only ACS in CHD). All these patients were examined for their serum level miR-92a in relation with blood lipid level, blood glucose level, and blood pressure. Patients of the DACS category represent higher levels of serum miR-92a in them which clearly makes it a promising diagnostic marker for detecting ACS in patients having T2DM.[64]
In a similar study, the serum level of miR-941 was checked in patients with stable angina (SA) and STEMI. When the examined serum results were compared then those patients who were suffering from STEMI had higher level of circulating miR-941 in their serum than those of the patient who has SA. Hence, the higher levels of the miR-941 in patients with STEMI confirmed that it can be used as an efficient diagnostic biomarker for CVD.[65]
In another case study, relation of the serum miRNA-499 and miRNA-210 was investigated against CVD. Patients with UA, non-STEMI (NSTEMI) (who had symptoms of chest pain which suggests that they may be suffering from ACS), and those having noncardiac chest pain (NCCP) were included. When their serum examination was done, then the patients who had NSTEMI and UA had elevated levels of both the miRNA-499 and miRNA-210 in comparison with those of the NCCP patients which makes both these miRNAs as effective biomarkers in the early diagnosis of ACS and other CHD.[66]
| Natural Products as Effective Therapeutic Agents | | |
Every year more than 5 million people have to go for the percutaneous coronary intervention (PCI) for the treatment of ACS.[67] Patients who are having the PCI also needs dual antiplatelet therapy (DAPT) along with the Clopidogrel (to block the receptors of P2Y12 signaling pathway) for the treatment of recurring events of chest pain and ischemic heart pains. However, the limitation of using only clopidogrel is that its antiplatelet response varies from individual to individual and can even increase the risk of ischemic events is patients with ACS. Moreover, patients having high platelet reactivity (HPR) can even suffer from stent thrombosis (ST) because of using clopidogrel as a single treatment.[68]
Natural products have re-gained the attention of researchers globally because of high-quality bioactive constituents and significant pharmacological properties.[69],[70],[71],[72],[73],[74],[75] Importantly, the identification of natural products having scientifically validated medicinal properties has skyrocketed. In the past few decades, pharmaceutical industry research into natural products has expanded at a breakneck pace.[76],[77],[78],[79] Emerging evidence has started to illuminate the ability of natural products to ameliorate ACS in animal models.
Salvianolate potentiated the anti-platelet effects of clopidogrel plus aspirin in ACS patients.[80] Salvianolic acid B inhibited aggregation of the platelets and GPIIb/IIIa activation induced by ADP. Moreover, VASP is an important substrate of PKA (cAMP-dependent protein kinase), which phosphorylates serine-157 of the 3 phosphorylation sites on VASP. Salvianolic acid B enhanced phosphorylation of VASP in ADP-stimulated platelets. Salvianolic acid B blocked the interactions between ADP and P2Y12 receptor.[80] Clinical trials have provided evidence about significant effects of anti-platelet drugs including clopidogrel, aspirin as well as GP IIb/IIIa inhibitors in ACS patients. ACS patients can reap benefits from combinatorial treatments consisting of salvianolate and standard anti-platelet therapies, which require further in-depth research.
Suxiao Jiuxin pills not only reduced adverse cardiovascular events but also improved heart function and quality of life of ACS patients.[81]
For the treatment of these disorders, Chinese medicine specialists have been using Tongxinluo capsules (TCs) with notable efficacy against these diseases.[82],[83] There are several pathways in human body which activates the platelets so to inhibit these platelets a single platelet therapy is ineffective.[84] Researchers used the antiplatelet therapy for the treatment of HPR in patients suffering from ACS. In addition to clopidogrel with DAPT they also used TCs, and the results displayed notable reduction in the HPR in ACS patients as compared to those who were treated with single clopidogrel.
Researchers investigated the use of Shexiang baoxin pills in individuals who were suffering from ACS with clopidogrel resistance. Patients having ACS along with the clopidogrel resistance were divided into two groups; one who was given the Shexiang baoxin pills along with that of the clopidogrel while the other group was treated with clopidogrel only. The platelet aggregation rate of the patients in the first group was quite less than that of the other one. Apart from that Shexiang baoxin pills in combination with the clopidogrel also enhanced the heart rate variability in patients with ACS.[85]
Maixuekang Capsule also has proven efficacy in reducing the platelet aggregation among ACS patients with ADP-induced platelet aggregation disorder.[86]
Future directions must emphasize on a better identification of traditional pharmacopeias to screen most potent and effective products which can ameliorate ACS.
| Concluding Remarks | | |
In this review, we have made efforts to provide a comprehensive landscape of the regulators which play instrumental role in the pathogenesis of ACS. Despite encouraging advancements in the biology and identification of clinically effective pharmacological targets, we still have to translate these findings more meaningfully in preclinical models.
Financial support and sponsorship
Nil.
Conflicts of interest
There are no conflicts of interest.
| References | | |
| 1. | Sanchis-Gomar F, Perez-Quilis C, Leischik R, Lucia A. Epidemiology of coronary heart disease and acute coronary syndrome. Ann Transl Med 2016;4:256.  |
| 2. | Overbaugh KJ. Acute coronary syndrome. Am J Nurs 2009;109:42-52. |
| 3. | McCarthy BD, Wong JB, Selker HP. Detecting acute cardiac ischemia in the emergency department: A review of the literature. J Gen Intern Med 1990;5:365-73. |
| 4. | Goodacre S, Locker T, Morris F, Campbell S. How useful are clinical features in the diagnosis of acute, undifferentiated chest pain? Acad Emerg Med 2002;9:203-8. |
| 5. | Biasucci LM, La Rosa G, Pedicino D, D'Aiello A, Galli M, Liuzzo G. Where does inflammation fit? Curr Cardiol Rep 2017;19:84. |
| 6. | Siadat ZD, Kiani K, Sadeghi M, Shariat AS, Farajzadegan Z, Kheirmand M. Association of vitamin D deficiency and coronary artery disease with cardiovascular risk factors. J Res Med Sci 2012;17:1052-5. |
| 7. | Nekouei ZK, Yousefy A, Doost HT, Manshaee G, Sadeghei M. Structural model of psychological risk and protective factors affecting on quality of life in patients with coronary heart disease: A psychocardiology model. J Res Med Sci 2014;19:90-8. |
| 8. | Gidron Y, Gilutz H, Berger R, Huleihel M. Molecular and cellular interface between behavior and acute coronary syndromes. Cardiovasc Res 2002;56:15-21. |
| 9. | Libby P. Molecular bases of the acute coronary syndromes. Circulation 1995;91:2844-50. |
| 10. | Cimmino G, Conte S, Morello A, D'Elia S, Marchese V, Golino P. The complex puzzle underlying the pathophysiology of acute coronary syndromes: From molecular basis to clinical manifestations. Expert Rev Cardiovasc Ther 2012;10:1533-43. |
| 11. | Surendran A, Atefi N, Zhang H, Aliani M, Ravandi A. Defining acute coronary syndrome through metabolomics. Metabolites 2021;11:685. |
| 12. | Franchini M. Genetics of the acute coronary syndrome. Ann Transl Med 2016;4:192. |
| 13. | Patay BA, Topol EJ. Is there a genetic basis for acute coronary syndrome? Nat Clin Pract Cardiovasc Med 2007;4:596-7. |
| 14. | Aronis KN, Moreno M, Polyzos SA, Moreno-Navarrete JM, Ricart W, Delgado E, et al. Circulating irisin levels and coronary heart disease: Association with future acute coronary syndrome and major adverse cardiovascular events. Int J Obes (Lond) 2015;39:156-61. |
| 15. | Pagidipati NJ, Peterson ED. Acute coronary syndromes in women and men. Nat Rev Cardiol 2016;13:471-80. |
| 16. | Farooqi AA, Attar R, Tanriover G, Sabitaliyevich UY, Zhailganov A, Rabandiyarov M. Regulation of NLRP3 by non-coding RNAs in different cancers: Interplay between non-coding RNAs and NLRP3 in carcinogenesis and metastasis. Cell Mol Biol (Noisy-le-grand) 2020;66:47-51. |
| 17. | Jo EK, Kim JK, Shin DM, Sasakawa C. Molecular mechanisms regulating NLRP3 inflammasome activation. Cell Mol Immunol 2016;13:148-59. |
| 18. | Swanson KV, Deng M, Ting JP. The NLRP3 inflammasome: Molecular activation and regulation to therapeutics. Nat Rev Immunol 2019;19:477-89. |
| 19. | Mangan MS, Olhava EJ, Roush WR, Seidel HM, Glick GD, Latz E. Targeting the NLRP3 inflammasome in inflammatory diseases. Nat Rev Drug Discov 2018;17:688. |
| 20. | Guo H, Callaway JB, Ting JP. Inflammasomes: Mechanism of action, role in disease, and therapeutics. Nat Med 2015;21:677-87. |
| 21. | Hoffman HM, Mueller JL, Broide DH, Wanderer AA, Kolodner RD. Mutation of a new gene encoding a putative pyrin-like protein causes familial cold autoinflammatory syndrome and Muckle-Wells syndrome. Nat Genet 2001;29:301-5. |
| 22. | Jafarizade M, Kahe F, Sharfaei S, Momenzadeh K, Pitliya A, Zahedi Tajrishi F, et al. The role of interleukin-27 in atherosclerosis: A contemporary review. Cardiology 2021;146:517-30. |
| 23. | Niyonzima N, Bakke SS, Gregersen I, Holm S, Sandanger Ø, Orrem HL, et al. Cholesterol crystals use complement to increase NLRP3 signaling pathways in coronary and carotid atherosclerosis. EBioMedicine 2020;60:102985. |
| 24. | Chanchal S, Mishra A, Singh MK, Ashraf MZ. Understanding inflammatory responses in the manifestation of prothrombotic phenotypes. Front Cell Dev Biol 2020;8:73. |
| 25. | Li Z, Guo J, Bi L. Role of the NLRP3 inflammasome in autoimmune diseases. Biomed Pharmacother 2020;130:110542. |
| 26. | Martínez GJ, Celermajer DS, Patel S. The NLRP3 inflammasome and the emerging role of colchicine to inhibit atherosclerosis-associated inflammation. Atherosclerosis 2018;269:262-71. |
| 27. | Altaf A, Qu P, Zhao Y, Wang H, Lou D, Niu N. NLRP3 inflammasome in peripheral blood monocytes of acute coronary syndrome patients and its relationship with statins. Coron Artery Dis 2015;26:409-21. |
| 28. | Malik J, Javed N, Ishaq U, Khan U, Laique T. Is there a role for colchicine in acute coronary syndromes? A literature review. Cureus 2020;12:e8166. |
| 29. | Martínez GJ, Robertson S, Barraclough J, Xia Q, Mallat Z, Bursill C, et al. Colchicine acutely suppresses local cardiac production of inflammatory cytokines in patients with an acute coronary syndrome. J Am Heart Assoc 2015;4:e002128. |
| 30. | Robertson S, Martínez GJ, Payet CA, Barraclough JY, Celermajer DS, Bursill C, et al. Colchicine therapy in acute coronary syndrome patients acts on caspase-1 to suppress NLRP3 inflammasome monocyte activation. Clin Sci (Lond) 2016;130:1237-46. |
| 31. | Parsamanesh N, Moossavi M, Bahrami A, Fereidouni M, Barreto G, Sahebkar A. NLRP3 inflammasome as a treatment target in atherosclerosis: A focus on statin therapy. Int Immunopharmacol 2019;73:146-55. |
| 32. | Su Q, Li L, Sun Y, Yang H, Ye Z, Zhao J. Effects of the TLR4/Myd88/NF-κB signaling pathway on NLRP3 inflammasome in coronary microembolization-induced myocardial injury. Cell Physiol Biochem 2018;47:1497-508. |
| 33. | Peng H, Wu H, Zhang G, Zhang W, Guo Y, Chang L, et al. Expression and clinical prognostic value of platelet NLRP3 in acute coronary syndrome. Int J Gen Med 2020;13:791-802. |
| 34. | Afrasyab A, Qu P, Zhao Y, Peng K, Wang H, Lou D, et al. Correlation of NLRP3 with severity and prognosis of coronary atherosclerosis in acute coronary syndrome patients. Heart Vessels 2016;31:1218-29. |
| 35. | Huang B, Qian Y, Xie S, Ye X, Chen H, Chen Z, et al. Ticagrelor inhibits the NLRP3 inflammasome to protect against inflammatory disease independent of the P2Y 12 signaling pathway. Cell Mol Immunol 2021;18:1278-89. |
| 36. | Xu HM, Sui FH, Sun MH, Guo GL. Downregulated microRNA-224 aggravates vulnerable atherosclerotic plaques and vascular remodeling in acute coronary syndrome through activation of the TGF-β/Smad pathway. J Cell Physiol 2019;234:2537-51. |
| 37. | Fitzsimons S, Oggero S, Bruen R, McCarthy C, Strowitzki MJ, Mahon NG, et al. microRNA-155 is decreased during atherosclerosis regression and is increased in urinary extracellular vesicles during atherosclerosis progression. Front Immunol 2020;11:576516. |
| 38. | Li S, Geng Q, Chen H, Zhang J, Cao C, Zhang F, et al. The potential inhibitory effects of miR-19b on vulnerable plaque formation via the suppression of STAT3 transcriptional activity. Int J Mol Med 2018;41:859-67. |
| 39. | Zhang W, Tang T, Nie D, Wen S, Jia C, Zhu Z, et al. IL-9 aggravates the development of atherosclerosis in ApoE-/- mice. Cardiovasc Res 2015;106:453-64. |
| 40. | Zheng Y, Wang Z, Deng L, Zhang G, Yuan X, Huang L, et al. Modulation of STAT3 and STAT5 activity rectifies the imbalance of Th17 and Treg cells in patients with acute coronary syndrome. Clin Immunol 2015;157:65-77. |
| 41. | Farooqi AA, Attar R, Yulaevna IM, Berardi R. Interaction of long non-coding RNAs and circular RNAs with microRNAs for the regulation of immunological responses in human cancers. Semin Cell Dev Biol. 2021 Jun 3:S1084-9521(21)00138-5. doi: 10.1016/j.semcdb.2021.05.029. |
| 42. | Farooqi AA, Naureen H, Attar R. Regulation of cell signaling pathways by circular RNAs and microRNAs in different cancers: Spotlight on Wnt/β-catenin, JAK/STAT, TGF/SMAD, SHH/GLI, NOTCH and Hippo pathways. Semin Cell Dev Biol. 2021 Apr 13:S1084-9521(21)00075-6. doi: 10.1016/j.semcdb.2021.04.002. |
| 43. | Farooqi AA, Qureshi MZ, Coskunpinar E, Naqvi SK, Yaylim I, Ismail M. MiR-421, miR-155 and miR-650: Emerging trends of regulation of cancer and apoptosis. Asian Pac J Cancer Prev 2014;15:1909-12. |
| 44. | Ekmekci CG, Coskunpinar E, Avci H, Farooqi AA, Orhan KS, Akbas F. Integrative analysis of mRNA and microRNA expression profiles in laryngeal squamous cell carcinoma. J Cell Biochem 2019;120:3415-22. |
| 45. | Wen R, Umeano AC, Essegian DJ, Sabitaliyevich UY, Wang K, Farooqi AA. Role of microRNA-410 in molecular oncology: A double edged sword. J Cell Biochem 2018;119:8737-42. |
| 46. | Volinia S, Calin GA, Liu CG, Ambs S, Cimmino A, Petrocca F, et al. A microRNA expression signature of human solid tumors defines cancer gene targets. Proc Natl Acad Sci U S A 2006;103:2257-61. |
| 47. | Lytle JR, Yario TA, Steitz JA. Target mRNAs are repressed as efficiently by microRNA-binding sites in the 5' UTR as in the 3' UTR. Proc Natl Acad Sci U S A 2007;104:9667-72. |
| 48. | Khraiwesh B, Arif MA, Seumel GI, Ossowski S, Weigel D, Reski R, et al. Transcriptional control of gene expression by microRNAs. Cell 2010;140:111-22. |
| 49. | Yu X, Xu JF, Song M, Zhang L, Li YH, Han L, et al. Associations of Circulating microRNA-221 and 222 With the Severity of Coronary Artery Lesions in Acute Coronary Syndrome Patients. Angiology. 2021 Jul 30:33197211034286. doi: 10.1177/00033197211034286. |
| 50. | Zhelankin AV, Stonogina DA, Vasiliev SV, Babalyan KA, Sharova EI, Doludin YV, et al. Circulating extracellular miRNA analysis in patients with stable CAD and acute coronary syndromes. Biomolecules 2021;11:962. |
| 51. | Li LJ, Gu YJ, Wang LQ, Wan W, Wang HW, Yang XN, et al. Serum exosomal microRNA-146a as a novel diagnostic biomarker for acute coronary syndrome. J Thorac Dis 2021;13:3105-14. |
| 52. | Yu J, Li Y, Leng D, Cao C, Yu Y, Wang Y. microRNA-3646 serves as a diagnostic marker and mediates the inflammatory response induced by acute coronary syndrome. Bioengineered 2021;12:5632-40. |
| 53. | Zhao B, Zhang Z, Gui L, Xiang Y, Sun X, Huang L. MiR-let-7i inhibits CD4+T cell apoptosis in patients with acute coronary syndrome. Adv Clin Exp Med 2021;30:779-88. |
| 54. | Tian S, Cao Y, Wang J, Bi Y, Zhong J, Meng X, et al. The miR-378c-Samd1 circuit promotes phenotypic modulation of vascular smooth muscle cells and foam cells formation in atherosclerosis lesions. Sci Rep 2021;11:10548. |
| 55. | Sun D, Ma T, Zhang Y, Zhang F, Cui B. Overexpressed miR-335-5p reduces atherosclerotic vulnerable plaque formation in acute coronary syndrome. J Clin Lab Anal 2021;35:e23608. |
| 56. | McCune C, Maynard S, McClements B, Lindsay JR. HbA1c for diabetes screening in acute coronary syndrome: Time for a reappraisal of the guidelines? Ulster Med J 2015;84:154-6. |
| 57. | Anderson JL, Adams CD, Antman EM, Bridges CR, Califf RM, Casey DE Jr., et al. 2011 ACCF/AHA focused update incorporated into the ACC/AHA 2007 guidelines for the management of patients with unstable angina/Non-ST-elevation myocardial infarction: A report of the American College of Cardiology Foundation/American Heart Association Task Force on Practice Guidelines. Circulation 2011;123:e426-579. |
| 58. | Cavusoglu E, Marmur JD, Chhabra S, Hojjati MR, Yanamadala S, Chopra V, et al. Elevated baseline plasma phospholipid protein (PLTP) levels are an independent predictor of long-term all-cause mortality in patients with diabetes mellitus and known or suspected coronary artery disease. Atherosclerosis 2015;239:503-8. |
| 59. | Wolsk E, Claggett B, Diaz R, Dickstein K, Gerstein HC, Køber L, et al. Increases in natriuretic peptides precede heart failure hospitalization in patients with a recent coronary event and type 2 diabetes mellitus. Circulation 2017;136:1560-2. |
| 60. | Müller KA, Rath D, Schmid M, Schoenleber H, Gawaz M, Geisler T, et al. High plasma levels of gremlin-1 and macrophage migration inhibitory factor, but not their ratio, indicate an increased risk for acute coronary syndrome in patients with type 2 diabetes mellitus. Clin Cardiol 2016;39:201-6. |
| 61. | Reid G, Kirschner MB, van Zandwijk N. Circulating microRNAs: Association with disease and potential use as biomarkers. Crit Rev Oncol Hematol 2011;80:193-208. |
| 62. | Wang L, Jin Y. Noncoding RNAs as biomarkers for acute coronary syndrome. Biomed Res Int 2020;2020:3298696. |
| 63. | Poller W, Dimmeler S, Heymans S, Zeller T, Haas J, Karakas M, et al. Non-coding RNAs in cardiovascular diseases: Diagnostic and therapeutic perspectives. Eur Heart J 2018;39:2704-16. |
| 64. | Wang W, Li Z, Zheng Y, Yan M, Cui Y, Jiang J. Circulating microRNA-92a level predicts acute coronary syndrome in diabetic patients with coronary heart disease. Lipids Health Dis 2019;18:22. |
| 65. | Bai R, Yang Q, Xi R, Li L, Shi D, Chen K. miR-941 as a promising biomarker for acute coronary syndrome. BMC Cardiovasc Disord 2017;17:227. |
| 66. | Shalaby SM, El-Shal AS, Shoukry A, Khedr MH, Abdelraheim N. Serum miRNA-499 and miRNA-210: A potential role in early diagnosis of acute coronary syndrome. IUBMB Life 2016;68:673-82. |
| 67. | Wiviott SD, Braunwald E, McCabe CH, Montalescot G, Ruzyllo W, Gottlieb S, et al. Prasugrel versus clopidogrel in patients with acute coronary syndromes. N Engl J Med 2007;357:2001-15. |
| 68. | Gurbel PA, Bliden KP, Hiatt BL, O'Connor CM. Clopidogrel for coronary stenting: Response variability, drug resistance, and the effect of pretreatment platelet reactivity. Circulation 2003;107:2908-13. |
| 69. | Butt G, Ozbey U, Malik DE, Attar R, Youssef L, Farooqi AA. Regulation of cell signaling pathways by Wogonin in different cancers: Mechanistic review. Cell Mol Biol (Noisy-le-grand) 2021;67:1-7. |
| 70. | Lin X, Attar R, Mobeen I, Yulaevna IM, Aras A, Butt G, et al. Regulation of cell signaling pathways by Schisandrin in different cancers: Opting for “Swiss Army Knife” instead of “Blunderbuss”. Cell Mol Biol (Noisy-le-grand) 2021;67:25-32. |
| 71. | Farooqi AA, Tahir F, Fakhar M, Butt G, Colombo Pimentel T, Wu N, et al. Antimetastatic effects of Citrus-derived bioactive ingredients: Mechanistic insights. Cell Mol Biol (Noisy-le-grand) 2021;67:178-86. |
| 72. | Xu B, Guo M, Ma L, Farooqi AA, Wang L, Qiao G, et al. Mere15, a novel polypeptide from Meretrix meretrix, inhibits proliferation and metastasis of human non-small cell lung cancer cells through regulating the PI3K/Akt/mTOR signaling pathway. Neoplasma 2021;68:1181-9. |
| 73. | Farooqi AA, Pinheiro M, Granja A, Farabegoli F, Reis S, Attar R, et al. EGCG mediated targeting of deregulated signaling pathways and non-coding RNAs in different cancers: Focus on JAK/STAT, Wnt/β-Catenin, TGF/SMAD, NOTCH, SHH/GLI, and TRAIL mediated signaling pathways. Cancers (Basel) 2020;12:951. |
| 74. | Farooqi AA, Sabitaliyevich UY. How far we have gone in realizing true potential of Viscum album as versatile regulator of cell signaling pathways. Cell Mol Biol (Noisy-le-grand) 2019;65:1-2. |
| 75. | Ozbey U, Attar R, Romero MA, Alhewairini SS, Afshar B, Sabitaliyevich UY, et al. Apigenin as an effective anticancer natural product: Spotlight on TRAIL, WNT/β-catenin, JAK-STAT pathways, and microRNAs. J Cell Biochem. 2018 Oct 2. doi: 10.1002/jcb.27575. |
| 76. | Qureshi MZ, Attar R, Romero MA, Sabitaliyevich UY, Nurmurzayevich SB, Ozturk O, et al. Regulation of signaling pathways by β-elemene in cancer progression and metastasis. J Cell Biochem 2019;120:12091-100. |
| 77. | Shahwar D, Iqbal MJ, Nisa MU, Todorovska M, Attar R, Sabitaliyevich UY, et al. Natural product mediated regulation of death receptors and intracellular machinery: Fresh from the pipeline about TRAIL-mediated signaling and natural TRAIL sensitizers. Int J Mol Sci 2019;20:2010. |
| 78. | Lin X, Farooqi AA. Cucurbitacin mediated regulation of deregulated oncogenic signaling cascades and non-coding RNAs in different cancers: Spotlight on JAK/STAT, Wnt/β-catenin, mTOR, TRAIL-mediated pathways. Semin Cancer Biol 2021;73:302-9. |
| 79. | Wang L, Cheng L, Ma L, Ahmad Farooqi A, Qiao G, Zhang Y, et al. Alnustone inhibits the growth of hepatocellular carcinoma via ROS- mediated PI3K/Akt/mTOR/p70S6K axis. Phytother Res 2022;36:525-42. |
| 80. | Liu L, Li J, Zhang Y, Zhang S, Ye J, Wen Z, et al. Salvianolic acid B inhibits platelets as a P2Y12 antagonist and PDE inhibitor: Evidence from clinic to laboratory. Thromb Res 2014;134:866-76. |
| 81. | Shen Z, Chen T, Deng B, Fan M, Hua J, Zhang M, et al. Effects on Suxiao jiuxin pills in the treatment of patients with acute coronary syndrome undergoing early percutaneous coronary intervention: A multicenter randomized double-blind placebo-controlled trial. J Altern Complement Med 2020;26:1055-63. |
| 82. | Li YN, Wang XJ, Li B, Liu K, Qi JS, Liu BH, et al. Tongxinluo inhibits cyclooxygenase-2, inducible nitric oxide synthase, hypoxia-inducible factor-2α/vascular endothelial growth factor to antagonize injury in hypoxia-stimulated cardiac microvascular endothelial cells. Chin Med J (Engl) 2015;128:1114-20. |
| 83. | Liu K, Wang XJ, Li YN, Li B, Qi JS, Zhang J, et al. Tongxinluo reverses the hypoxia-suppressed claudin-9 in cardiac microvascular endothelial cells. Chin Med J (Engl) 2016;129:442-7. |
| 84. | Zhang L, Li Y, Yang BS, Li L, Wang XZ, Ge ML, et al. A multicenter, randomized, double-blind, and placebo-controlled study of the effects of tongxinluo capsules in acute coronary syndrome patients with high on-treatment platelet reactivity. Chin Med J (Engl) 2018;131:508-15. |
| 85. | Zhang L, Liu N, Zhang J, Zhang H. Effect of Shexiang baoxin pills on clopidogrel resistance in patients with acute coronary syndrome. Pak J Pharm Sci 2016;29:2303-6. |
| 86. | Ge CJ, Yuan F, Feng LX, Lv SZ, Liu H, Song XT, et al. Clinical effect of Maixuekang Capsule [INSIDE:1] on long-term prognosis in patients with acute coronary syndrome after percutaneous coronary intervention. Chin J Integr Med 2014;20:88-93. |
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