Long non-coding RNAs and tyrosine kinase-mediated drug resistance in pancreatic cancer

Dangran Li1, Shiting Weng2, Kai Zeng3

  • 1Key Laboratory of Carbohydrate Chemistry and Biotechnology, Ministry of Education, School of Life Sciences and Health Engineering, Jiangnan University, Wuxi 214122, China; The State Key Laboratory of Pharmaceutical Biotechnology, College of Life Sciences, Nanjing University, Nanjing 210029, China.

Gene
|November 19, 2023
PubMed

Insights

Pancreatic cancer drug resistance is linked to tyrosine kinases (TKs) and long non-coding RNAs (lncRNAs). Targeting these molecules offers potential for new pancreatic cancer treatments and biomarkers.

Area of Science:

  • Oncology
  • Molecular Biology
  • Genetics

Background:

  • Pancreatic cancer (PC) exhibits high malignancy and poor survival rates, largely due to chemoresistance.
  • Dysfunctional tyrosine kinases (TKs) and long non-coding RNAs (lncRNAs) are implicated in PC drug resistance and prognosis.

Purpose of the Study:

  • To summarize mechanisms of TKs and lncRNAs in mediating PC drug resistance and malignant phenotypes.
  • To explore the roles and regulatory mechanisms of lncRNAs in PC drug resistance.
  • To highlight the clinical significance and therapeutic potential of TKs and lncRNAs in PC.

Main Methods:

  • Literature review and synthesis of existing research on TKs and lncRNAs in pancreatic cancer.
  • Analysis of molecular mechanisms involving lncRNA-protein and lncRNA-microRNA interactions.
  • Examination of lncRNAs as upstream regulators of TKs.

Main Results:

  • TKs and lncRNAs significantly influence pancreatic cancer drug resistance and overall prognosis.
  • lncRNAs can act as oncogenes or tumor suppressors, employing diverse mechanisms to affect drug resistance.
  • lncRNAs regulate TKs, contributing to chemoresistance in pancreatic cancer.

Conclusions:

  • Specific TKs (AXL, EGFR, IGF1R, MET) and lncRNAs (LINC00460, PVT1, HIF1A-AS1) have clinical significance in pancreatic cancer.
  • TKs and lncRNAs represent promising diagnostic/prognostic biomarkers and potential therapeutic targets for overcoming pancreatic cancer drug resistance.

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