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:Immune microenvironment and immunotherapy in hepatocellular carcinoma: mechanisms and advances.
Immune microenvironment and immunotherapy in hepatocellular carcinoma: mechanisms and advances.
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肝细胞癌(HCC)仍是全球癌症相关死亡的主要原因之一。肿瘤微环境(TME)在HCC进展中发挥关键作用,其特征为基质成分、免疫细胞与肿瘤细胞之间的动态相互作用。肿瘤相关巨噬细胞(TAM)、TIL(肿瘤浸润淋巴细胞)、细胞毒性T淋巴细胞(CTL)、调节性T细胞(Treg)、髓源性抑制细胞(MDSC)、树突状细胞(DC)及自然杀伤(NK)细胞等关键免疫细胞参与免疫逃逸和肿瘤进展。免疫检查点抑制剂(ICI)、癌症疫苗、过继细胞治疗(ACT)和联合疗法等免疫治疗进展显示出增强抗肿瘤应答的潜力。双重ICI联合、ICI与分子靶向药物联合,以及与局部治疗或放疗结合,均已改善HCC患者结局。本综述介绍对HCC免疫微环境的认识进展,并强调免疫治疗策略在HCC管理中的治疗潜力。
Hepatocellular carcinoma (HCC) remains a leading cause of cancer-related mortality globally. The tumor microenvironment (TME) plays a pivotal role in HCC progression, characterized by dynamic interactions between stromal components, immune cells, and tumor cells. Key immune players, including tumor-associated macrophages (TAMs), tumor-infiltrating lymphocytes (TILs), cytotoxic T lymphocytes (CTLs), regulatory T cells (Tregs), MDSCs, dendritic cells (DCs), and natural killer (NK) cells, contribute to immune evasion and tumor progression.
Recent advances in immunotherapy, such as immune checkpoint inhibitors (ICIs), cancer vaccines, adoptive cell therapy (ACT), and combination therapies, have shown promise in enhancing anti-tumor responses. Dual ICI combinations, ICIs with molecular targeted drugs, and integration with local treatments or radiotherapy have demonstrated improved outcomes in HCC patients. This review highlights the evolving understanding of the immune microenvironment and the therapeutic potential of immunotherapeutic strategies in HCC management.
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