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FBW7-MCL-1 轴在 M1 和 M2 巨噬细胞相关的结肠癌细胞进展中起关键作用:验证靶向 PI3Kγ 的免疫治疗价值。

The FBW7-MCL-1 axis is key in M1 and M2 macrophage-related colon cancer cell progression: validating the immunotherapeutic value of targeting PI3Kγ.

机构信息

Sungkyunkwan University School of Medicine, Seoul, Republic of Korea.

Institute for Future Medicine Samsung Medical Center, Seoul, Republic of Korea.

出版信息

Exp Mol Med. 2020 May;52(5):815-831. doi: 10.1038/s12276-020-0436-7. Epub 2020 May 22.

Abstract

Colorectal cancer is a devastating disease with a low 5-year survival rate. Recently, many researchers have studied the mechanisms of tumor progression related to the tumor microenvironment. Here, we addressed the prognostic value of tumor-associated macrophages (TAMs) using a total of 232 CRC patient tissue samples and investigated the mechanisms underlying TAM-related colon cancer progression with respect to PI3Kγ regulation using in vitro, in vivo, and ex vivo approaches. Patients with M2/M1 < 3 had significantly improved progression-free survival and overall survival compared with patients with M2/M1 > 3. M1 and M2 macrophages elicited opposite effects on colon cancer progression via the FBW7-MCL-1 axis. Blocking macrophage PI3Kγ had cytotoxic effects on colon cancer cells and inhibited epithelial-mesenchymal transition features by regulating the FBW7-MCL-1 axis. The results of this study suggest that macrophage PI3Kγ may be a promising target for immunotherapy in colon cancer.

摘要

结直肠癌是一种具有低 5 年生存率的毁灭性疾病。最近,许多研究人员研究了与肿瘤微环境相关的肿瘤进展机制。在这里,我们使用总共 232 例 CRC 患者组织样本研究了肿瘤相关巨噬细胞 (TAMs) 的预后价值,并使用体外、体内和离体方法研究了 PI3Kγ 调节的 TAM 相关结肠癌进展的机制。与 M2/M1 > 3 的患者相比,M2/M1 < 3 的患者无进展生存期和总生存期显著改善。M1 和 M2 巨噬细胞通过 FBW7-MCL-1 轴对结肠癌进展产生相反的影响。阻断巨噬细胞 PI3Kγ 通过调节 FBW7-MCL-1 轴对结肠癌细胞具有细胞毒性作用并抑制上皮-间充质转化特征。这项研究的结果表明,巨噬细胞 PI3Kγ 可能是结肠癌免疫治疗的一个有前途的靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4fe3/7272616/ebd922b69f27/12276_2020_436_Fig1_HTML.jpg

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