Multiple Myeloma (MM) is a genetically complex cancer that has a higher incidence and mortality in males when compared to females. These sex differences are well-documented epidemiologically, yet their biological mechanisms remain uncharacterized. We hypothesized that sex-specific genetic regulations from somatic mutations affect MM cells gene expression differently in each sex and subsequently lead to differential functional genetic dependency between the two sexes. To test this, we first identified genes with sex-biased expression in MM, then identified sex-specific somatic regulators of these genes, evaluated their association with overall survival outcomes, and finally assessed their functional importance using CRISPR-Cas9 dependency screens in MM cell lines. Our findings provide the systematic evidence that sex-differentiated somatic regulation underlies tumor-intrinsic mechanisms in MM, establishing the importance of incorporating sex-aware molecular analyses for improved biomarker discovery and precision medicine. Collectively, these results establish sex as a fundamental biological variable in MM with significant implications for disease outcomes.
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Ajibola Opakunle
Yuting Shan
Yingbo Huang
Human Genetics and Genomics Advances
University of Minnesota
Northwestern University
University of Colorado Anschutz Medical Campus
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Opakunle et al. (Sun,) studied this question.
www.synapsesocial.com/papers/69ca1210883daed6ee094de3 — DOI: https://doi.org/10.1016/j.xhgg.2026.100596