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蟾毒灵通过调节M2巨噬细胞极化抑制转移性结直肠癌的免疫逃逸。

Bufalin inhibits immune escape in metastatic colorectal cancer by regulating M2 macrophage polarization.

作者信息

Lu Chang, Shang Jing, Xie Manli, Zhu Yuan, Zhong Jiani, He Yujie, Xiao Zengyou, Chen Wen, Yang Ze-An, Tang Xiaoxia, Yin Peihao, Chen Jinbao

机构信息

Department of General Surgery, Putuo Hospital, Shanghai University of Traditional Chinese Medicine, Shanghai, 200062, China.

Fifth Clinical Medical College, Anhui Medical University, Hefei, 230022, Anhui, China.

出版信息

Apoptosis. 2025 Apr 5. doi: 10.1007/s10495-025-02107-y.

Abstract

The prognosis for patients with metastatic colorectal cancer (mCRC) remains poor primarily owing to immune escape caused by immunosuppressive tumor microenvironment (TME). M2 tumor-associated macrophages (TAMs) have been considered as a pivotal role in sustaining the immunosuppressive character in TME. Our previous studies have found that highly mCRC cells could promote M2 TAMs polarization, leading to the exhaustion of T cell antitumor immunity. Studies have reported that Bufalin (BU) could reverse the immunosuppressive TME via regulating TAMs polarization, but the mechanisms underlying remain elusive. In this study, we demonstrated that KLF4 secreted by highly mCRC cells not only promoted the polarization to M2 TAMs but also up-regulated the PD-L1 expression in TAMs, leading to suppressing cytotoxic T lymphocyte (CTL) function to facilitate tumor immune escape. Mechanistically, BU targeted the SRC-3 protein to reduce KLF4 release in highly mCRC cells to regulate the polarization of M2 TAMs and down-regulate PD-L1 expression in TAMs, resulting in reprogramming of the TME and enhancing the anti-tumor immunity. These results have also been validated in both subcutaneous tumor models and orthotopic tumor models. Overall, this research further elucidates the anti-tumor mechanism of BU for inhibiting immune escape in mCRC and facilitate exploitation of a new potential macrophage-based mCRC immunotherapeutic modality.

摘要

转移性结直肠癌(mCRC)患者的预后仍然很差,主要是由于免疫抑制性肿瘤微环境(TME)导致的免疫逃逸。M2肿瘤相关巨噬细胞(TAM)被认为在维持TME的免疫抑制特性中起关键作用。我们之前的研究发现,高转移mCRC细胞可促进M2 TAM极化,导致T细胞抗肿瘤免疫耗竭。有研究报道,蟾毒灵(BU)可通过调节TAM极化来逆转免疫抑制性TME,但其潜在机制仍不清楚。在本研究中,我们证明高转移mCRC细胞分泌的KLF4不仅促进向M2 TAM极化,还上调TAM中PD-L1的表达,导致细胞毒性T淋巴细胞(CTL)功能受抑制,从而促进肿瘤免疫逃逸。机制上,BU靶向SRC-3蛋白以减少高转移mCRC细胞中KLF4的释放,从而调节M2 TAM极化并下调TAM中PD-L1的表达,导致TME重编程并增强抗肿瘤免疫力。这些结果在皮下肿瘤模型和原位肿瘤模型中均得到验证。总体而言,本研究进一步阐明了BU抑制mCRC免疫逃逸的抗肿瘤机制,并有助于开发一种基于巨噬细胞的新型mCRC免疫治疗方法。

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