{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,1,14]],"date-time":"2026-01-14T14:33:48Z","timestamp":1768401228934,"version":"3.49.0"},"reference-count":108,"publisher":"Portland Press Ltd.","issue":"11","license":[{"start":{"date-parts":[[2019,10,11]],"date-time":"2019-10-11T00:00:00Z","timestamp":1570752000000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/creativecommons.org\/licenses\/by\/4.0\/"}],"content-domain":{"domain":["portlandpress.com"],"crossmark-restriction":true},"short-container-title":[],"published-print":{"date-parts":[[2019,11,29]]},"abstract":"<jats:title>Abstract<\/jats:title>\n               <jats:p>Long noncoding RNAs (lncRNAs), more than 200 nt in length, are functional molecules found in various species. These lncRNAs play a vital role in cell proliferation, differentiation, and degeneration and are also involved in pathophysiological processes of cancer and neurodegenerative, autoimmune, and cardiovascular diseases (CVDs). In recent years, emerging challenges for intervention studies on ischemic heart diseases have received much attention. LncRNAs have a key function in the alleviation of myocardial infarction (MI) injury and myocardial ischemia\u2013reperfusion injury. During cardiac hypertrophy (CH) and fibrosis, cardiac cells undergo structural changes and become dysfunctional due to the effects of neurohormonal factors. LncRNAs may serve as important therapeutic targets that promote cardiac remodeling and then retard the development of heart failure (HF). In addition, studies on the roles and mechanisms of action of lncRNAs participating in cardiac pathophysiology via other factors have become the focus of research worldwide. Here, we review the current knowledge on various lncRNAs and their functions in cardiac biology, particularly concentrating on ischemic heart disease, CH, and cardiac fibrosis. We next discuss the predictive value of lncRNAs as diagnostic biomarkers of CVDs.<\/jats:p>","DOI":"10.1042\/bsr20190966","type":"journal-article","created":{"date-parts":[[2019,10,11]],"date-time":"2019-10-11T12:43:46Z","timestamp":1570797826000},"update-policy":"https:\/\/doi.org\/10.1042\/crossmark_policy","source":"Crossref","is-referenced-by-count":26,"title":["The roles of long noncoding RNAs in myocardial pathophysiology"],"prefix":"10.1042","volume":"39","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-3023-5498","authenticated-orcid":false,"given":"Cheng","family":"Chen","sequence":"first","affiliation":[{"name":"Department of Pathophysiology, Xiangya School of Medicine, Central South University, Changsha 410000, Hunan, P.R. China"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Yuting","family":"Tang","sequence":"additional","affiliation":[{"name":"Department of Pathophysiology, Xiangya School of Medicine, Central South University, Changsha 410000, Hunan, P.R. China"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Hui","family":"Sun","sequence":"additional","affiliation":[{"name":"Department of Pathophysiology, Xiangya School of Medicine, Central South University, Changsha 410000, Hunan, P.R. China"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Xiaofang","family":"Lin","sequence":"additional","affiliation":[{"name":"Department of Pathophysiology, Xiangya School of Medicine, Central South University, Changsha 410000, Hunan, P.R. China"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0001-9544-7224","authenticated-orcid":false,"given":"Bimei","family":"Jiang","sequence":"additional","affiliation":[{"name":"Department of Pathophysiology, Xiangya School of Medicine, Central South University, Changsha 410000, Hunan, P.R. China"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"288","published-online":{"date-parts":[[2019,11,12]]},"reference":[{"key":"2021111619521107600_B1","doi-asserted-by":"publisher","first-page":"372","DOI":"10.1016\/j.devcel.2017.10.026","article-title":"HBL1 is a human long noncoding rNA that modulates cardiomyocyte development from pluripotent stem cells by counteracting MIR1","volume":"43","author":"Liu","year":"2017","journal-title":"Dev. 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