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Male-biased Yap1-Cd276/B7-H3 axis for immune evasion in medulloblastoma.

Cancer cell 2026 Vol.44(4) p. 760-776.e8

Abdelfattah N, Natarajan S, Tran HN, Wong T, Faisal M, Maldonado J, McMinimy R, Borland H, Chen SH, Zhao H, Vasquez M, Rodriguez FF, Wagner CR, Camargo F, Olson J, George J, Yun K

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Molecular mechanisms underlying sex-specific differences in cancer incidence and therapy responses are under intense investigation.

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BibTeX ↓ RIS ↓
APA Abdelfattah N, Natarajan S, et al. (2026). Male-biased Yap1-Cd276/B7-H3 axis for immune evasion in medulloblastoma.. Cancer cell, 44(4), 760-776.e8. https://doi.org/10.1016/j.ccell.2026.01.005
MLA Abdelfattah N, et al.. "Male-biased Yap1-Cd276/B7-H3 axis for immune evasion in medulloblastoma.." Cancer cell, vol. 44, no. 4, 2026, pp. 760-776.e8.
PMID 41650973

Abstract

Molecular mechanisms underlying sex-specific differences in cancer incidence and therapy responses are under intense investigation. Here, we report sex-biased functions of Yap1 in multiple cancer types in human and mouse. Through integrated multi-omics analyses, we demonstrate that Yap1 deletion significantly extends survival in male but not female Sonic Hedgehog (SHH) medulloblastomas (MB) models. While Yap1 is required to maintain stem-like cells in both sexes, Yap1 plays a more critical role in immune evasion in males. Mechanistically, YAP1 is essential for activating Cd276/B7-H3 expression to mediate CD8 T cell suppression in males. Consistently, CD276 inhibition extends survival in male but not female SHH MB. Moreover, in vivo targets of YAP1 stratify survival in male but not female patients with medulloblastoma, glioblastoma, mesothelioma, and lung cancer. This study provides evidence for sex-biased functions of Yap1 and CD276 in MB immune suppression and highlights the importance of biological sex in cancer:immune interactions.

MeSH Terms

Humans; Medulloblastoma; Male; Animals; Female; YAP-Signaling Proteins; Mice; B7 Antigens; Adaptor Proteins, Signal Transducing; Cerebellar Neoplasms; Tumor Escape; Transcription Factors; Sex Factors; CD8-Positive T-Lymphocytes; Gene Expression Regulation, Neoplastic