癌症研究
癌症
血红素加氧酶
医学
巨噬细胞
免疫学
病理
血红素
化学
内科学
体外
生物化学
酶
作者
M. Bahri,Taha Al‐Adhami,Emre Demirel,Jit Sarkar,Karen Feehan,Joanne E. Anstee,Tik Shing Cheung,Dominika Sosnowska,Chloé Woodman,William Macmorland,Dorothy Yang,James Rosekilly,Renee Gitsaki-Taylor,Cheryl Gillett,Cheryl L. Scudamore,James Spicer,Khondaker Miraz Rahman,James N. Arnold
标识
DOI:10.1126/scitranslmed.ads3085
摘要
A subset of perivascular tumor-associated macrophages (PvTAMs) expressing lymphatic vessel endothelial hyaluronan receptor–1 (LYVE-1) relies on heme oxygenase–1 (HO-1) activity to maintain an immunologically cold tumor microenvironment, which suppresses the efficacy of chemotherapy. Consequently, HO-1 inhibition represents a strategy to target immunosuppressive LYVE-1 + PvTAMs and improve therapeutic responses. We developed and characterized KCL-HO-1i, a small-molecule, orally bioavailable HO-1 inhibitor. In chemotherapy-resistant spontaneous murine MMTV-PyMT breast cancer and subcutaneous MN/MCA1 sarcoma models, targeting the PvTAM function with KCL-HO-1i enhanced chemotherapy effects and sensitized tumors to treatment. KCL-HO-1i combined with chemotherapy promoted an immunologically hot tumor microenvironment characterized by increased infiltration of CD8 + T cells exhibiting effector function. These findings identify KCL-HO-1i as a nontoxic, orally bioavailable small-molecule immunotherapeutic targeting a key subset of protumoral PvTAMs, offering a combinatorial strategy to enhance chemotherapy efficacy in cancer.
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