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Editorial: The intricate innate immune-cancer cell relationship in the context of tumor angiogenesis, immunity and microbiota: The angiogenic switch in the tumor microenvironment as a key target for immunotherapies
Editorial: The intricate innate immune-cancer cell relationship in the context of tumor angiogenesis, immunity and microbiota: The angiogenic switch in the tumor microenvironment as a key target for immunotherapies
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Editorial: The intricate innate immune-cancer cell relationship in the context of tumor angiogenesis, immunity and microbiota: The angiogenic switch in the tumor microenvironment as a key target for immunotherapies
Editorial: The intricate innate immune-cancer cell relationship in the context of tumor angiogenesis, immunity and microbiota: The angiogenic switch in the tumor microenvironment as a key target for immunotherapies

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Editorial: The intricate innate immune-cancer cell relationship in the context of tumor angiogenesis, immunity and microbiota: The angiogenic switch in the tumor microenvironment as a key target for immunotherapies
Editorial: The intricate innate immune-cancer cell relationship in the context of tumor angiogenesis, immunity and microbiota: The angiogenic switch in the tumor microenvironment as a key target for immunotherapies
Journal Article

Editorial: The intricate innate immune-cancer cell relationship in the context of tumor angiogenesis, immunity and microbiota: The angiogenic switch in the tumor microenvironment as a key target for immunotherapies

2022
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Overview
[...]there are many promising preclinical and trials data in NSCLC, where in parallel with classical ICIs targeting PD-1/PD-L1, new target molecules could be used, such as: [...]they shed new light on the possibility of administering fecal microbiota transplantation to modulate the gut microbiota in cancer treatment. The ICP score showed reliability and efficacy in predicting the survival of patients with gliomas, in pan-cancer samples, and six independent cancer types. [...]the ICP score was correlated with the genomic alteration features in gliomas, exhibited a remarkable association with multiple immunomodulators that could potentially mediate immune escape, and predicted immunotherapeutic responses with a high sensitivity.

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