Cell death & disease · 2026
CXCR2 blockade potentiates HDAC3 deletion mediated antitumor immunity in colorectal cancer.
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Zhang Yukun, Yu Yeping, Yang Fang, Zhao ZiHeng, Gu Xiaodong, Li Zhenyang, Zhou Yiming, Zhang Wenqian, Chen Huichun, Xiang Jianbin
Аннотация
HDAC3 is highly expressed in colorectal cancer (CRC) and associated with poor prognosis. This study reveals that HDAC3 deletion dually regulates chemokine expression through epigenetic mechanisms, promoting CD8⁺ T cell infiltration (via CXCL10) on one hand, while enhancing the recruitment of myeloid-derived suppressor cells (MDSCs) (via CXCL1/2/3/5) on the other. The latter, mediated through CXCR2 signaling, counteracts the intrinsic anti-tumor effect of HDAC3 deletion. We further demonstrate that combining a CXCR2 inhibitor effectively blocks MDSC infiltration and significantly enhances the immunotherapeutic efficacy mediated by HDAC3 deletion. This study systematically elucidates the "double-edged sword" role of HDAC3 in the CRC immune microenvironment and provides a theoretical and experimental basis for an HDAC3/CXCR2 dual-targeting therapeutic strategy.