Long non-coding RNA (lncRNA) H19 in human cancer: From proliferation and metastasis to therapy

癌症研究 长非编码RNA 肿瘤进展 转移 生物 基因沉默 癌症 小RNA 表观遗传学 细胞生长 下调和上调 基因 遗传学
作者
Mehrdad Hashemi,Marzieh Sadat Moosavi,Hedyeh Maghareh Abed,Maryam Dehghani,Masoumeh Aalipour,Elaheh Ali Heydari,Mitra Behroozaghdam,Maliheh Entezari,Shokooh Salimimoghadam,Emine Selda Gündüz,Afshin Taheriazam,Sepideh Mirzaei,Saeed Samarghandian
出处
期刊:Pharmacological Research [Elsevier BV]
卷期号:184: 106418-106418 被引量:182
标识
DOI:10.1016/j.phrs.2022.106418
摘要

Initiation and development of cancer depend on multiple factors that mutations in genes and epigenetic level can be considered as important drivers. Epigenetic factors include a large family of members and understanding their function in cancer has been a hot topic. LncRNAs are RNA molecules with no capacity in synthesis of proteins, and they have regulatory functions in cells. LncRNAs are localized in nucleus and cytoplasm, and their abnormal expression is related to development of tumor. This manuscript emphasizes on the role of lncRNA H19 in various cancers and its association with tumor hallmarks. The function of lncRNA H19 in most tumors is oncogenic and therefore, tumor cells increase its expression for promoting their progression. LncRNA H19 contributes to enhancing growth and cell cycle of cancers and by EMT induction, it is able to elevate metastasis rate. Silencing H19 induces apoptotic cell death and disrupts progression of tumors. LncRNA H19 triggers chemo- and radio-resistance in cancer cells. miRNAs are dually upregulated/down-regulated by lncRNA H19 in increasing tumor progression. Anti-cancer agents reduce lncRNA H19 in impairing tumor progression and increasing therapy sensitivity. A number of downstream targets and molecular pathways for lncRNA H19 have been detected in cancers including miRNAs, RUNX1, STAT3, β-catenin, Akt2 and FOXM1. Clinical studies have revealed potential of lncRNA H19 as biomarker and its association with poor prognosis. LncRNA H19 can be transferred to cancer cells via exosomes in enhancing their progression.
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