The emerging role of micrornas in regulating the drug response of cholangiocarcinoma

Wen Kuan Huang, Chun Nan Yeh*

*Corresponding author for this work

Research output: Contribution to journalReview articlepeer-review

8 Scopus citations

Abstract

Cholangiocarcinoma (CCA) is the most common biliary malignancy, and has a poor prognosis. The median overall survival with the standard‐of‐care chemotherapy (Gemcitabine and cisplatin) in patients with advanced‐stage CCA is less than one year. The limited efficacy of chemotherapy or targeted therapy remains a major obstacle to improving survival. The mechanisms involved in drug resistance are complex. Research efforts focusing on the distinct molecular mechanisms underlying drug resistance should prompt the development of treatment strategies that overcome chemoresistance or targeted drug resistance. MicroRNAs (miRNAs) are a class of evolutionarily conserved, short noncoding RNAs regulating gene expression at the post-transcriptional level. Dysregulated miRNAs have been shown to participate in almost all CCA hallmarks, including cell proliferation, migration and invasion, apoptosis, and the epithelial‐to-mesenchymal transition. Emerging evidence demonstrates that miRNAs play a role in regulating responses to chemotherapy and targeted therapy. Herein, we present an overview of the current knowledge on the miRNA‐mediated regulatory mechanisms underlying drug resistance among CCA. We also discuss the application of miRNA‐based therapeutics to CCA, providing the basis for innovative treatment approaches.

Original languageEnglish
Article number1396
Pages (from-to)1-22
Number of pages22
JournalBiomolecules
Volume10
Issue number10
DOIs
StatePublished - 10 2020

Bibliographical note

Publisher Copyright:
© 2020 by the authors. Licensee MDPI, Basel, Switzerland.

Keywords

  • Chemotherapy
  • Cholangiocarcinoma
  • Cisplartin
  • Drug resistance
  • Gemcitabine
  • MicroRNAs
  • Targeted therapy

Fingerprint

Dive into the research topics of 'The emerging role of micrornas in regulating the drug response of cholangiocarcinoma'. Together they form a unique fingerprint.

Cite this