Abstract
The emergence of therapeutic resistance remains the primary challenge to achieving durable responses in cancer treatment, thereby limiting the long-term e"cacy of several chemotherapies and targeted agents. Resistance may develop through diverse and often overlapping mechanisms. Conventional approaches to overcome resistance, such as dose escalation or combination regimens, are frequently constrained by systemic toxicity and adaptive tumor evolution. Moreover, many central drivers of resistance, including transcription factors and non-enzymatic regulatory proteins, remain inaccessible to therapeutics. Small interfering
RNAs (siRNAs) o#er a fundamentally distinct and pathway-centric approach to overcoming drug resistance by enabling sequence-specific degradation of resistance-associated messenger RNAs. By acting upstream of protein synthesis, siRNA therapeutics can directly suppress both druggable and traditionally undruggable
targets, including e$ux transporters, anti-apoptotic regulators, DNA repair enzymes, epigenetic modifiers, epithelial-mesenchymal transition transcription factors, and key oncogenic drivers such as KRAS and MYC. Advances in chemical modification and delivery platforms have significantly improved siRNA stability, specificity, and pharmacokinetic durability, enabling sustained gene silencing in vivo. The current review examines the molecular principles of siRNA-induced gene silencing and evaluates the current siRNA-based strategies targeting key mechanisms of chemotherapy resistance. Preclinical and translational studies demonstrating
the reversal of multidrug resistance, restoration of apoptotic sensitivity, disruption of DNA repair–mediated
tolerance, and suppression of adaptive oncogenic signaling are highlighted. In addition, the emerging clinical
trials that validate siRNA-based approaches in cancer treatment are summerized.
Cite this article as: Bardaweel SK, Hajjo R,
Sabbah DA, Qasem DA. Small interfering
RNA strategies to overcome drug resistance
in cancer: pathway targeting and translational
advances. Eurasian J Med. 2026, 58(1), 1350,
doi:10.5152/eurasianjmed.2026.251350.
Similar Articles

This work is licensed under a Creative Commons Attribution 4.0 International License.