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Ribosomal Proteins in Blood Exosomes as Markers of an Unfavorable Prognosis in Patients with Breast Cancer Full article

Journal Asian Pacific Journal of Cancer Prevention
ISSN: 1513-7368 , E-ISSN: 2476-762X
Output data Year: 2026, Volume: 27, Number: 7, Pages: 2497-2508 Pages count : 12 DOI: 10.31557/apjcp.2026.27.7.2497
Tags Exosomes; EVs; ribosomal proteins; breast cancer; biomarkers
Authors Shefer Aleksei 1,2 , Babaylova Elena 1,2 , Yanshole Lyudmila 3 , Grygoreva Alina 2 , Svarovsky Dmitry 4 , Graifer Dmitri 2 , Malygin Alexey 2 , Chernyshovа Alyona 5,1 , Tamkovich Svetlana 5,1
Affiliations
1 Institute of Medicine and Medical Technologies, Novosibirsk State University, Novosibirsk, Russia
2 Knorre Institute of Chemical Biology and Fundamental Medicine, Siberian Branch of Russian Academy of Sciences, Novovsibirsk, Russia
3 International Tomography Center, Siberian Branch of Russian Academy of Sciences, Novosibirsk, Russia
4 Cancer Research Institute, Tomsk National Research Medical Center, Russian Academy of Sciences, Tomsk, Russia
5 E.N. Meshalkin National Medical Research Center, Ministry of Health of the Russian Federation, Novosibirsk, Russia

Abstract: Introduction: Exosomes, extracellular vesicles (EVs) 30-150 nm in diameter, are known to mediate intercellular communication by transferring bioactive molecules that can reprogram recipient cell phenotypes. Our analysis of 5-year survival data from breast cancer patients (BCPs) revealed that the poorest outcomes were exclusively associated with conserved signature of three ribosomal proteins (RPs) - MRPL52, RPL28, and RPL40 (UBA52) - that were completely absent in healthy females (HFs) and better-prognosis cases. Strikingly, all patients with this exosomal RP profile succumbed to metastatic relapse within the observation period. Methods: While RPs are known components of tumor-derived exosomes, their absence in EVs from normal cells suggests cancer-specific sorting mechanisms. To investigate this, we characterized exosomal RP cargo from three breast cancer cell lines (MCF-7, BT-474, BT-549), finding cell-type-specific RP patterns that differed from the clinical BC signature. Transfection of BT-549 cells with FLAG-tagged RPS3 (an aggressive cancer-associated RP) induced dramatic changes in exosomal RP composition, including the appearance of RPL28 - matching our clinical findings. Results: Bioinformatic analysis revealed that the RPs identified in BCP blood exosomes (MRPL52, RPL28, RPL40, RPS6) are associated with poor prognosis across multiple cancers and participate in key oncogenic pathways. Conclusion: The concordance between our clinical and experimental data suggests that: (a) specific RPs are selectively packaged into exosomes under stress conditions; (b) this process may contribute to BC aggressiveness; (c) exosomal RP profiling could serve as a novel prognostic approach. These findings illuminate previously unrecognized roles of ribosomal components in cancer progression through EV-mediated communication.
Cite: Shefer A. , Babaylova E. , Yanshole L. , Grygoreva A. , Svarovsky D. , Graifer D. , Malygin A. , Chernyshovа A. , Tamkovich S.
Ribosomal Proteins in Blood Exosomes as Markers of an Unfavorable Prognosis in Patients with Breast Cancer
Asian Pacific Journal of Cancer Prevention. 2026. V.27. N7. P.2497-2508. DOI: 10.31557/apjcp.2026.27.7.2497 Scopus OpenAlex
Dates:
Submitted: Aug 5, 2025
Accepted: Jul 13, 2026
Published online: Jul 26, 2026
Identifiers:
≡ Scopus: 2-s2.0-105046187024
≡ OpenAlex: W7171673463
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