Colorectal cancer (CRC), a malignant tumor worldwide consists of microsatellite instability (MSI) and stable (MSS) phenotypes. Although SHP2 is a hopeful target for cancer therapy, its relationship with innate immunosuppression remains elusive. To address that, single-cell RNA sequencing was performed to explore the role of SHP2 in all cell types of tumor microenvironment (TME) from murine MC38 xenografts. Intratumoral cells were found to be functionally heterogeneous and responded significantly to SHP099, a SHP2 allosteric inhibitor. The malignant evolution of tumor cells was remarkably arrested by SHP099. Mechanistically, STING-TBK1-IRF3-mediated type I interferon signaling was highly activated by SHP099 in infiltrated myeloid cells. Notably, CRC patients with MSS phenotype exhibited greater macrophage infiltration and more potent SHP2 phosphorylation in CD68+ macrophages than MSI-high phenotypes, suggesting the potential role of macrophagic SHP2 in TME. Collectively, our data reveals a mechanism of innate immunosuppression mediated by SHP2, suggesting that SHP2 is a promising target for colon cancer immunotherapy.
Keywords: APC, antigen-presenting cell; BTLA, B- and T-lymphocyte attenuator; CNVs, copy number variations; CRC, colorectal cancer; Colorectal cancer; DSBs, double-strand breaks; GSEA, gene set enrichment analysis; KRAS, Kirsten rat sarcoma viral oncogene homolog; MAPK, mitogen-activated kinase; MSI, microsatellite instability; MSS, microsatellite stable; Macrophage; PCA, principal component analysis; PD-1, programmed cell death 1; PTPN11; SHP099; STING; STING, stimulator of interferon genes; TME, tumor microenvironment; Tumor microenvironment; Type I interferon; scRNA-seq; scRNA-seq, single-cell RNA-sequencing; t-SNE, t-distributed stochastic neighbor embedding.
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