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Updated: Jan 15, 2026

Sequencing Small Non-coding RNA from Formalin-fixed Tissues and Serum-derived Exosomes from Castration-resistant Prostate Cancer Patients
Published on: November 19, 2019
INTERPLAY OF LNCRNAS, METABOLIC CELL DEATH, AND IMMUNE MICROENVIRONMENT IN GENITOURINARY MALIGNANCIES
V Gordiiuk1, L Shevchenko1, D Todoryshyn2
1Institute of Molecular Biology and Genetics, the NAS of Ukraine, Kyiv, Ukraine.
None:
Genitourinary cancers, including prostate, bladder, and renal cancers, represent a significant global health burden due to their high prevalence and resistance to conventional therapies. A critical aspect of cancer progression is metabolic reprogramming, which not only fuels uncontrolled growth but also profoundly influences programmed cell death pathways and the tumor immune microenvironment. This review synthesizes current research on the intricate roles of long non-coding RNAs (lncRNAs) in modulating three emerging forms of regulated cell death - cuproptosis, ferroptosis, and disulfidptosis - within the context of genitourinary malignancies. We discuss how specific lncRNA signatures are implicated in the regulation of these metabolic cell death pathways, affecting cancer cell proliferation, migration, and invasion. Furthermore, we explore the compelling association between these lncRNA expression patterns and the characteristics of the tumor immune microenvironment, highlighting their potential as prognostic biomarkers and indicators for stratifying patient responses to immunotherapy. The evidence presented underscores the multifaceted functions of lncRNAs in cancer metabolism and immunity, positioning them as promising therapeutic targets and informative biomarkers for precision oncology in genitourinary cancers.
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