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:Advances in immune checkpoint inhibitor combination strategies for microsatellite stable colorectal cancer.
Advances in immune checkpoint inhibitor combination strategies for microsatellite stable colorectal cancer.
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免疫检查点抑制剂已经重塑了多种肿瘤类型的预后,包括具有微卫星不稳定性(MSI)的转移性结直肠肿瘤。然而,90-95%的转移性结直肠肿瘤为微卫星稳定(MSS),免疫治疗在此类肿瘤中未能显示出有意义的临床结果。MSS结直肠肿瘤被认为是免疫冷肿瘤。已提出多种因素来解释这种对免疫检查点阻断缺乏应答的现象,包括TIL(肿瘤浸润淋巴细胞)水平低、肿瘤突变负荷低、WNT/β-catenin通路突变率高,以及肝转移与免疫抑制相关。然而,基于免疫检查点抑制剂的新型联合治疗研究在MSS结直肠癌中显示出有前景的活性。在此,我们综述了阻碍免疫治疗活性的潜在生物学事实,并详细介绍了已评估的不同免疫检查点抑制剂联合方案,以及新型免疫基础疗法,以克服MSS结直肠癌中的先天耐药机制。
Immune checkpoint inhibitors have reshaped the prognostic of several tumor types, including metastatic colorectal tumors with microsatellite instability (MSI).
However, 90-95% of metastatic colorectal tumors are microsatellite stable (MSS) in which immunotherapy has failed to demonstrate meaningful clinical results. MSS colorectal tumors are considered immune-cold tumors. Several factors have been proposed to account for this lack of response to immune checkpoint blockade including low levels of tumor infiltrating lymphocytes, low tumor mutational burden, a high rate of WNT/β-catenin pathway mutations, and liver metastases which have been associated with immunosuppression.
However, studies with novel combinations based on immune checkpoint inhibitors are showing promising activity in MSS colorectal cancer.
Here, we review the underlying biological facts that preclude immunotherapy activity, and detail the different immune checkpoint inhibitor combinations evaluated, along with novel immune-based therapies, to overcome innate mechanisms of resistance in MSS colorectal cancer.
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