Tumor Exosomal HIF2A Induce Peritumoral M2 Macrophages Accumulation to Facilitate Intestinal Invasion in Colorectal Cancer

作者：Dan Wang, Qingyang Lei, Yang Li, Yachang Huo, Weina Yu, Shasha Liu, Yangfei Duan, Shumin Feng, Zhen Li, Jinbo Liu, Zhenqiang Sun, Weitang Yuan, Lihua Liu, Bin Zhang, Yi Zhang · 发表于：Theranostics · 年份：2025 · DOI：10.7150/thno.113190 · 被引用次数：5 · 研究领域：Vascular Tumors and Angiosarcomas

Background: Local intestinal invasion of tumor cells often leads to recurrent and refractory colorectal cancer (CRC).However, the driven mechanism is not fully understood.Methods: A total of 145 patients with CRC and 10 patients with intestinal perforations or benign lesions were randomly enrolled.The distribution and clinical relevance of macrophages in different tissues were determined by flow cytometry and immunohistochemistry. PCR screening and RNA-sequencing analysis were used to explore the regulatory mechanisms.The functions of macrophages were further verified using an orthotopic mouse model of Csf1r cre Cxcr4 fl/fl mice.Results: Here, we unveil the role of M2 macrophages in local intestinal invasion.M2 macrophages infiltrated more in peritumor tissues than in tumor and normal tissues of CRC patients, which were significantly associated with the tumor local intestinal invasion and recurrence.Macrophage elimination attenuated local intestinal invasion.Mechanistically, CXCL12 is highly expressed in peritumor tissues and recruits monocytes and polarizes them into M2 macrophages by binding to CXCR4.Furthermore, HIF-2-containing exosomes from primary colorectal tumor cells promoted CXCL12 secretion by peritumoral fibroblasts through HIF-2 binding to the CXCL12 promoter, which in turn induced M2 macrophage accumulation and tumor cell invasion.Macrophage-specific deletion of CXCR4 or knockdown of HIF2A in colorectal tumor cells reduced M2 accumulation in peritumor tissue and...