Abstract 2801: SRY-mediated upregulation of PD-L1 promotes immune evasion in hepatocellular carcinoma and contributes to sex-specific disparities in immunotherapy response

Abstract Background: The impact of sex chromosomes on the tumor microenvironment (TME) is significant, beyond hormonal effects. This study investigates the role of the sex-determining gene SRY in the immune microenvironment of hepatocellular carcinoma (HCC), focusing on how SRY regulates immune checkpoints and contributes to gender disparities in immunotherapy response. Methods: Multiple HCC mouse models (chemically induced, hydrodynamic, orthotopic, subcutaneous) using SRY transgenic knockout (KO) or knock-in (KI) mice were employed. To eliminate hormonal effects, the mice were castrated. Flow cytometry, immunofluorescence, and ELISA assessed T cell changes in the TME. Cellular models used PCR array, CUT&Tag, qPCR, WB, and luciferase assays to explore SRY’s transcriptional regulation. Clinical samples validated correlations between SRY, immune markers, and PD-L1. Results: •In castrated male SRY-KO mice, increased CD8+ T cells and elevated GZMB, TNF-α, and IFN-γ were observed in the TME.•SRY-KI in castrated males reduced CD8+ T cells and functional markers.•Ectopic SRY in castrated females similarly impaired T cell infiltration and function.•PCR array in SRY-overexpressing HCC cells revealed upregulation of PD-L1.•CUT&Tag and luciferase assays confirmed SRY binds the IRF1 promoter, upregulating IRF1 expression.•IRF1 knockdown abolished PD-L1 upregulation, confirming an SRY-IRF1-PD-L1 axis.•In vivo, PD-L1 knockdown in SRY-overexpressing tumors reversed immune suppression and tumor growth.•Anti-PD-L1 treatment showed enhanced efficacy in SRY-overexpressing tumors.•Clinical HCC samples confirmed positive SRY-PD-L1 correlation and negative SRY-CD8+ T cell correlation. Conclusions: SRY, a male-specific gene, regulates the immune checkpoint PD-L1 via IRF1, suppressing CD8+ T cell function in the TME. Targeting the SRY-IRF1-PD-L1 axis may improve immunotherapy outcomes, especially in male HCC patients. The text has been translated and polished using AI. Citation Format: Bingyi Ren, Kai Sheng, Yichen Yang, . SRY-mediated upregulation of PD-L1 promotes immune evasion in hepatocellular carcinoma and contributes to sex-specific disparities in immunotherapy response [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 2801.

Authors

Institutions

Publication Details

Journal
Cancer Research
Published
2026-04-03
DOI
https://doi.org/10.1158/1538-7445.am2026-2801
Primary Topic
interferon and immune responses
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Abstract 2801: SRY-mediated upregulation of PD-L1 promotes immune evasion in hepatocellular carcinoma and contributes to sex-specific disparities in immunotherapy response

Yichen Yang, Bingyi Ren, Kai Sheng
Cancer Research
interferon and immune responses
article

Abstract 2801: SRY-mediated upregulation of PD-L1 promotes immune evasion in hepatocellular carcinoma and contributes to sex-specific disparities in immunotherapy response

Yichen Yang, Bingyi Ren, Kai Sheng
article en

Abstract

Abstract Background: The impact of sex chromosomes on the tumor microenvironment (TME) is significant, beyond hormonal effects. This study investigates the role of the sex-determining gene SRY in the immune microenvironment of hepatocellular carcinoma (HCC), focusing on how SRY regulates immune checkpoints and contributes to gender disparities in immunotherapy response. Methods: Multiple HCC mouse models (chemically induced, hydrodynamic, orthotopic, subcutaneous) using SRY transgenic knockout (KO) or knock-in (KI) mice were employed. To eliminate hormonal effects, the mice were castrated. Flow cytometry, immunofluorescence, and ELISA assessed T cell changes in the TME. Cellular models used PCR array, CUT&Tag, qPCR, WB, and luciferase assays to explore SRY’s transcriptional regulation. Clinical samples validated correlations between SRY, immune markers, and PD-L1. Results: •In castrated male SRY-KO mice, increased CD8+ T cells and elevated GZMB, TNF-α, and IFN-γ were observed in the TME.•SRY-KI in castrated males reduced CD8+ T cells and functional markers.•Ectopic SRY in castrated females similarly impaired T cell infiltration and function.•PCR array in SRY-overexpressing HCC cells revealed upregulation of PD-L1.•CUT&Tag and luciferase assays confirmed SRY binds the IRF1 promoter, upregulating IRF1 expression.•IRF1 knockdown abolished PD-L1 upregulation, confirming an SRY-IRF1-PD-L1 axis.•In vivo, PD-L1 knockdown in SRY-overexpressing tumors reversed immune suppression and tumor growth.•Anti-PD-L1 treatment showed enhanced efficacy in SRY-overexpressing tumors.•Clinical HCC samples confirmed positive SRY-PD-L1 correlation and negative SRY-CD8+ T cell correlation. Conclusions: SRY, a male-specific gene, regulates the immune checkpoint PD-L1 via IRF1, suppressing CD8+ T cell function in the TME. Targeting the SRY-IRF1-PD-L1 axis may improve immunotherapy outcomes, especially in male HCC patients. The text has been translated and polished using AI. Citation Format: Bingyi Ren, Kai Sheng, Yichen Yang, . SRY-mediated upregulation of PD-L1 promotes immune evasion in hepatocellular carcinoma and contributes to sex-specific disparities in immunotherapy response [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 2801.

Cancer ResearchVol. 86(7_Supplement)
First Affiliated Hospital of Xi'an Jiaotong University (CN), First Hospital of Xi'an (CN)
Gender equality
Openalex Percentile: Top 7%
interferon and immune responses
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.