4.5 Review

The emerging role of long non-coding RNA in gallbladder cancer pathogenesis

Journal

BIOCHIMIE
Volume 132, Issue -, Pages 152-160

Publisher

ELSEVIER FRANCE-EDITIONS SCIENTIFIQUES MEDICALES ELSEVIER
DOI: 10.1016/j.biochi.2016.11.007

Keywords

Long non-coding RNA; LncRNAs; Gallbladder cancer; Oncogenes; Tumor suppressors; Biomarkers; Diagnostic markers; Prognostic markers

Funding

  1. Department of Science and Technology of India through the Ramanujan fellowship [SR/S2/RJN-95/2011]
  2. NIH/NCI grant [CA093729]
  3. Department of Biotechnology, India [6242-P30/RGCB/PMD/DBT/AKJN/2015]
  4. Central University Punjab, Bathinda [GP-25]

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Gallbladder cancer (GBC) is the most common and aggressive form of biliary tract carcinoma with an alarmingly low 5-year survival rate. Despite its high mortality rate, the underlying mechanisms of GBC pathogenesis are not completely understood. Recently, from a growing volume of literature, long non coding RNAs (lncRNAs) have emerged as key regulators of gene expression and appear to play vital roles in many human cancers. To date, a number of IncRNAs have been implicated in GBC, but their potential roles in GBC have not been systematically examined. Thus, in this review, we critically discuss the emerging roles of IncRNAs in GBC, and the pathways involved. Specifically, we note that some IncRNAs show greater expression in T1 and T2 tumor stages compared to T3 and T4 tumor stages and that their dysregulation leads to alterations in cell cycle progression and can cause an increase in GBC cell proliferation or apoptosis. In addition, some IncRNAs control the epithelial-mesenchymal transition process, while others take part in the regulation of ERK/MAPK and Ras cancer-associated signaling pathways. We also present their potential utility in diagnosis, prognosis, and/or treatment of GBC. The overall goal of this review is to stimulate interest in the role of IncRNAs in GBC, which may open new avenues in the determination of GBC pathogenesis and may lead to the development of new preventive and therapeutic strategies for GBC. (C) 2016 Elsevier B.V. and Societe Francaise de Biochimie et Biologie Moleculaire (SFBBM). All rights reserved.

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