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Updated: Jul 10, 2025

Using RNA-sequencing to Detect Novel Splice Variants Related to Drug Resistance in In Vitro Cancer Models
Published on: December 9, 2016
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.
Abstract:
Pancreatic cancer (PC) is one of the most malignant tumors with a dismal survival rate, this is primarily due to inevitable chemoresistance. Dysfunctional tyrosine kinases (TKs) and long non-coding RNAs (lncRNAs) affect the drug resistance and prognosis of PC. Here, we summarize the mechanisms by which TKs or lncRNAs mediate drug resistance and other malignant phenotypes. We also discuss that lncRNAs play oncogenic or tumor suppressor roles and different mechanisms including lncRNA-proteins/microRNAs to mediate drug resistance. Furthermore, we highlight that lncRNAs serve as upstream regulators of TKs mediating drug resistance. Finally, we display the clinical significance of TKs (AXL, EGFR, IGF1R, and MET), clinical trials, and lncRNAs (LINC00460, PVT1, HIF1A-AS1). In the future, TKs and lncRNAs may become diagnostic and prognostic biomarkers or drug targets to overcome the drug resistance of PC.
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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