RNF43 p.G659fs 通过 PI3K/AKT/mTOR 信号通路和 HLA-E 上调导致 MSI-high 结直肠癌中 NK 细胞功能障碍
RNF43 p.G659fs leads to natural killer cell dysfunction in MSI-high colorectal cancer through PI3K/AKT/mTOR signaling and HLA-E up-regulation.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Boosting immune system against cancer by resveratrol.
Boosting immune system against cancer by resveratrol.
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免疫系统的调节是包括免疫治疗、化疗和放疗在内的抗癌治疗的关键部分。癌症治疗中免疫调节的目的是增强免疫系统细胞,包括CD8+ T淋巴细胞和自然杀伤(NK)细胞,同时抑制巨噬细胞和调节性T细胞(Tregs)的免疫抑制反应。通常,使用单一或双重模式可以诱导针对癌症的免疫系统反应。然而,免疫抑制反应会在癌症治疗后减弱抗肿瘤免疫。使用某些药物增强免疫系统对抗癌症的功能,可以提高抗癌治疗的治疗效率。白藜芦醇作为一种天然药物,已显示出调节免疫系统以增强抗肿瘤免疫的能力。白藜芦醇已被证明能诱导抗癌细胞因子如IFN-γ和TNF-α的释放,并抑制TGF-β的释放。它还能刺激CD4+ T细胞和巨噬细胞向抗癌细胞极化,并减少免疫抑制细胞的浸润和极化。此外,白藜芦醇可以使癌细胞对抗癌免疫细胞释放的死亡信号敏感。本综述阐述了白藜芦醇如何通过调节肿瘤内的免疫细胞反应来增强免疫系统对抗癌症。
Modulation of the immune system is a critical part of anticancer therapies including immunotherapy, chemotherapy, and radiotherapy. The aim of immunomodulation in cancer therapy is boosting immune system cells including CD8+ T lymphocytes and natural killer (NK) cells, as well as suppression of immunosuppressive responses by macrophages and regulatory T cells (Tregs). Usually, using single or dual modality can induce immune system responses against cancer.
However, immunosuppressive responses attenuate antitumor immunity following cancer therapy. Using some agents to boost immune system's function against cancer can increase therapeutic efficiency of anticancer therapy. Resveratrol, as a natural agent, has shown ability to modulate the immune system to potentiate antitumor immunity.
Resveratrol has been shown to induce the release of anticancer cytokines such as IFN-γ and TNF-α and also inhibits the release of TGF-β. It also can stimulate the polarization of CD4+ T cells and macrophages toward anticancer cells and reduce infiltration and polarization of immunosuppressive cells.
Furthermore, resveratrol can sensitize cancer cells to the released dead signals by anticancer immune cells. This review explains how resveratrol can boost the immune system against cancer via modulation of immune cell responses within tumor.
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