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How is CD39 involved in colorectal cancer? 


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CD39 is involved in colorectal cancer by promoting immune exhaustion, impairing antitumor immune activity, and increasing CRC progression . CD39 is upregulated in both primary and metastatic colorectal tumors, suggesting its relevance as a molecular target for T-cell engineering . Tumor-infiltrating T cells in colorectal tumors co-express CD39 along with multiple inhibitory receptors, indicating their exhaustion status . CD39 disruption in T cells using CRISPR/Cas9 technology has been shown to improve the adoptive T cell therapy of colorectal cancer . CD39 disruption, combined with the genetic disruption of the endogenous T cell receptor (TCR), generates triple-knockout T cells that exhibit a functional advantage in recognizing and killing colorectal cancer cells . These findings suggest that targeting CD39 in T cells could be a promising approach for the treatment of colorectal cancer .

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CD39 contributes to immunosuppressive activity of T cells and poor prognosis in colorectal cancer.
CD39 is coexpressed with CD103 on cytotoxic T cells in colorectal cancers with low mutation burden, indicating its involvement in identifying neoantigen-specific T cells.
CD39 is found to be a major driver of exhaustion in both primary and metastatic colorectal tumors, making it a potential molecular target for T cell engineering in the treatment of colorectal cancer.
CD39 is found to be the major driver of exhaustion in both primary and metastatic colorectal tumors.

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