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Updated: Jul 4, 2025

Using RNA-sequencing to Detect Novel Splice Variants Related to Drug Resistance in In Vitro Cancer Models
Published on: December 9, 2016
RNA binding proteins in cancer chemotherapeutic drug resistance
Hemanathan Vembuli1,2, Ravi Gor1, Satish Ramalingam1
1Department of Genetic Engineering, School of Bio-Engineering, SRM Institute of Science and Technology, Kattankulathur, Tamil Nadu, India.
Abstract:
Drug resistance has been a major obstacle in the quest for a cancer cure. Many chemotherapeutic treatments fail to overcome chemoresistance, resulting in tumor remission. The exact process that leads to drug resistance in many cancers has not been fully explored or understood. However, the discovery of RNA binding proteins (RBPs) has provided insight into various pathways and post-transcriptional gene modifications involved in drug tolerance. RBPs are evolutionarily conserved proteins, and their abnormal gene expression has been associated with cancer progression. Additionally, RBPs are aberrantly expressed in numerous neoplasms. RBPs have also been implicated in maintaining cancer stemness, epithelial-to-mesenchymal transition, and other processes. In this review, we aim to provide an overview of RBP-mediated mechanisms of drug resistance and their implications in cancer malignancy. We discuss in detail the role of major RBPs and their correlation with noncoding RNAs (ncRNAs) that are associated with the inhibition of chemosensitivity. Understanding and exploring the pathways of RBP-mediated chemoresistance will contribute to the development of improved cancer diagnosis and treatment strategies.
Insights
RNA binding proteins (RBPs) drive chemoresistance in cancer by altering gene expression and promoting cancer stemness. Understanding these RBP-mediated mechanisms is crucial for developing new cancer therapies.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Drug resistance is a significant challenge in cancer treatment, leading to therapeutic failure.
- RNA binding proteins (RBPs) play critical roles in post-transcriptional gene regulation and are implicated in cancer progression.
- Aberrant RBP expression is observed in various neoplasms and contributes to cancer stemness and epithelial-to-mesenchymal transition.
Purpose of the Study:
- To review the mechanisms of chemoresistance mediated by RNA binding proteins (RBPs).
- To explore the implications of RBP-mediated drug resistance in cancer malignancy.
- To discuss the correlation between RBPs, noncoding RNAs (ncRNAs), and the inhibition of chemosensitivity.
Main Methods:
- Literature review of studies on RNA binding proteins and chemoresistance.
- Analysis of RBP roles in cancer stemness and epithelial-to-mesenchymal transition.
- Examination of RBP interactions with noncoding RNAs in the context of drug resistance.
Main Results:
- RBPs are key regulators of gene expression involved in developing chemoresistance.
- Abnormal RBP expression is linked to cancer progression and poor treatment outcomes.
- RBPs, in conjunction with ncRNAs, actively suppress chemosensitivity.
Conclusions:
- Understanding RBP-mediated chemoresistance pathways is vital for advancing cancer treatment.
- Targeting RBPs and their associated ncRNAs may offer novel therapeutic strategies.
- Further research into RBP functions can improve cancer diagnosis and therapeutic interventions.
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