Differential Expression of Caveolin-3, Suppression of Tumorigenicity 2, and Growth Differentiation Factor-15 Genes and Their Association with Acute Myocardial Infarction: A Cross-Sectional Study in a Multi-Specialty Hospital in Tamil Nadu

被引:2
作者
Venugopal, Priyanka [1 ]
Logu, Kannika [2 ]
Balakrishnan, Karthikeyan [2 ]
Subbaih, Usha [3 ]
Kandadai, Sriram Damal [4 ]
George, Melvin [1 ]
机构
[1] Hindu Mission Hosp, Clin Res, Chennai 600045, India
[2] Hindu Mission Hosp, Cardiol, Chennai, India
[3] Bharath Inst Higher Educ & Res BIHER, Sree Balaji Dent Coll & Hosp, Human Genet Res Ctr, Chennai, India
[4] Hindu Mission Hosp, Diabetol & Endocrinol, Chennai, India
关键词
caveolin-3; pathogenesis; fibrosis; myocardial infarction; markers; BLOOD-CELL COUNT; NATRIURETIC-PEPTIDE; HEART; OVEREXPRESSION; BIOMARKER; ST2;
D O I
10.1089/gtmb.2022.0162
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Background: Acute myocardial infarction (AMI) is one of the world's leading causes of cardiovascular death. Recent studies have reported the influence of the genes caveolin-3 (CAV3), suppression of tumorigenicity 2, and growth differentiating factor-15 in cardiovascular diseases, especially myocardial infarction, but their role and function remain unclear. Hence, this study was designed to evaluate the expression levels of these three genes in AMI and understanding the role of CAV-3 in the pathogenesis of AMI.Methods and Results: Blood samples were collected from 50 AMI patients and 50 non-AMI controls in this cross-sectional study. Relative expression levels of the three genes were performed using real-time PCR. Bioinformatics tools were used for functional gene enrichment and protein-protein interactions. CAV-3 was significantly upregulated among AMI patients compared to controls. In silico analyses identified CAV-3 as playing critical roles in smooth muscle contraction, cardiac conduction, and calcium-mediated transport via binding with essential proteins including dysferlin and annexinsConclusion: This study is a first of its kind, reporting an upregulation of CAV-3 in AMI patients. The expression of all three genes significantly influenced the systolic function of the heart in AMI patients. A more in-depth understanding of CAV-3 in the pathophysiology of AMI is essential and it may prove to be a novel.
引用
收藏
页码:109 / 119
页数:11
相关论文
共 27 条
[1]  
[Anonymous], 2011, Cardiovascular disease
[2]   Transgenic overexpression of caveolin-3 in the heart induces a cardiomyopathic phenotype [J].
Aravamudan, B ;
Volonte, D ;
Ramani, R ;
Gursoy, E ;
Lisanti, MP ;
London, B ;
Galbiati, F .
HUMAN MOLECULAR GENETICS, 2003, 12 (21) :2777-2788
[3]   Housekeeping gene expression stability in reproductive tissues after mitogen stimulation [J].
Arenas-Hernandez M. ;
Vega-Sanchez R. .
BMC Research Notes, 6 (1)
[4]   UniProt: the universal protein knowledgebase in 2021 [J].
Bateman, Alex ;
Martin, Maria-Jesus ;
Orchard, Sandra ;
Magrane, Michele ;
Agivetova, Rahat ;
Ahmad, Shadab ;
Alpi, Emanuele ;
Bowler-Barnett, Emily H. ;
Britto, Ramona ;
Bursteinas, Borisas ;
Bye-A-Jee, Hema ;
Coetzee, Ray ;
Cukura, Austra ;
Da Silva, Alan ;
Denny, Paul ;
Dogan, Tunca ;
Ebenezer, ThankGod ;
Fan, Jun ;
Castro, Leyla Garcia ;
Garmiri, Penelope ;
Georghiou, George ;
Gonzales, Leonardo ;
Hatton-Ellis, Emma ;
Hussein, Abdulrahman ;
Ignatchenko, Alexandr ;
Insana, Giuseppe ;
Ishtiaq, Rizwan ;
Jokinen, Petteri ;
Joshi, Vishal ;
Jyothi, Dushyanth ;
Lock, Antonia ;
Lopez, Rodrigo ;
Luciani, Aurelien ;
Luo, Jie ;
Lussi, Yvonne ;
Mac-Dougall, Alistair ;
Madeira, Fabio ;
Mahmoudy, Mahdi ;
Menchi, Manuela ;
Mishra, Alok ;
Moulang, Katie ;
Nightingale, Andrew ;
Oliveira, Carla Susana ;
Pundir, Sangya ;
Qi, Guoying ;
Raj, Shriya ;
Rice, Daniel ;
Lopez, Milagros Rodriguez ;
Saidi, Rabie ;
Sampson, Joseph .
NUCLEIC ACIDS RESEARCH, 2021, 49 (D1) :D480-D489
[5]   Heart Failure [J].
Braunwald, Eugene .
JACC-HEART FAILURE, 2013, 1 (01) :1-20
[6]   MG53 nucleates assembly of cell membrane repair machinery [J].
Cai, Chuanxi ;
Masumiya, Haruko ;
Weisleder, Noah ;
Matsuda, Noriyuki ;
Nishi, Miyuki ;
Hwang, Moonsun ;
Ko, Jae-Kyun ;
Lin, Peihui ;
Thornton, Angela ;
Zhao, Xiaoli ;
Pan, Zui ;
Komazaki, Shinji ;
Brotto, Marco ;
Takeshima, Hiroshi ;
Ma, Jianjie .
NATURE CELL BIOLOGY, 2009, 11 (01) :56-U108
[7]   Paper Caveolin-3 protects diabetic hearts from acute myocardial infarction/reperfusion injury through β2AR, cAMP/PKA, and BDNF/TrkB signaling pathways [J].
Gong, Jiaji ;
Zhou, Fan ;
Xie, Simin ;
Wang, Xin ;
Xu, Junmei ;
Xiao, Feng .
AGING-US, 2020, 12 (14) :14300-14313
[8]   Caveolae and caveolins in the cardiovascular system [J].
Gratton, JP ;
Bernatchez, P ;
Sessa, WC .
CIRCULATION RESEARCH, 2004, 94 (11) :1408-1417
[9]   The association between white blood cell count and acute myocardial infarction in-hospital mortality: Findings from the national registry of myocardial infarction [J].
Grzybowski, M ;
Welch, RD ;
Parsons, L ;
Ndumele, CE ;
Chen, E ;
Zalenski, R ;
Barron, HV .
ACADEMIC EMERGENCY MEDICINE, 2004, 11 (10) :1049-1060
[10]   Cardiac-Specific Overexpression of Caveolin-3 Attenuates Cardiac Hypertrophy and Increases Natriuretic Peptide Expression and Signaling [J].
Horikawa, Yousuke T. ;
Panneerselvam, Mathivadhani ;
Kawaraguchi, Yoshitaka ;
Tsutsumi, Yasuo M. ;
Ali, Sameh S. ;
Balijepalli, Ravi C. ;
Murray, Fiona ;
Head, Brian P. ;
Niesman, Ingrid R. ;
Rieg, Timo ;
Vallon, Volker ;
Insel, Paul A. ;
Patel, Hemal H. ;
Roth, David M. .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2011, 57 (22) :2273-2283