Sungkyunkwan University School of Medicine, Seoul, Republic of Korea.
Institute for Future Medicine Samsung Medical Center, Seoul, Republic of Korea.
Exp Mol Med. 2020 May;52(5):815-831. doi: 10.1038/s12276-020-0436-7. Epub 2020 May 22.
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.
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。