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This metabolite specifically targets and stabilizes PD-L1, which suppresses the activity of tumor-infiltrating T lymphocytes and leads to increased recruitment and activity of polymorphonuclear myeloid-derived suppressor cells (PMN-MDSCs) and tumor-associated macrophages (TAMs) ( In microsatellite stable (MSS) colorectal cancer, tumor cells exhibit asynchronous disruption of the cholesterol biosynthesis pathway, leading to the accumulation of distal cholesterol precursors such as desmosterol and zymosterol

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treatment led to complete cessation of tumor growth