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Updated: Sep 19, 2025

Implementation of In Vitro Drug Resistance Assays: Maximizing the Potential for Uncovering Clinically Relevant Resistance Mechanisms
Published on: December 9, 2015
A review on ribosomal protein S3 (RPS3): Roles in cancer and its resistance to drugs
Tae-Sung Kim1, Yong Weon Yi1, Dong Joon Kim2
1Department of Biochemistry, College of Medicine, Dankook University, Cheonan-si 31116, Chungcheongnam-do, Republic of Korea; Multidrug-Resistant Refractory Cancer Convergence Research Center (MRCRC), Dankook University, Cheonan-si 31116, Chungcheongnam-do, Republic of Korea.
Abstract:
Ribosomal protein S3 (RPS3) is a component of the small subunit of the eukaryotic ribosome, contributing to ribosome maturation and the initiation of translation. In addition to its canonical roles, accumulating evidence highlights a range of extra-ribosomal functions for RPS3 in diverse cellular processes. Notably, RPS3 enhances activation of the nuclear factor κ-light-chain-enhancer of activated B cells (NF-κB) pathway by interacting with the P65 subunit of the NF-κB complex. Given that NF-κB pathway is implicated in tumorigenesis and resistance to anticancer therapies, RPS3-mediated activation of this pathway suggests a potential role for RPS3 in cancer progression and drug resistance. Supporting this, elevated RPS3 expression has been observed in malignant tumors, despite the generally ubiquitous expression of RPS3 mRNA and protein is normal human tissues without notable tissue- or cell-type specificity. Despite these observations, the roles of RPS3 in oncogenic processes and its clinical implications insufficiently characterized. In this review, we examine the current literature to explore the contribution of RPS3 to cancer development and drug resistance.
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