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Wnt5a/CaMKII/ERK/CCL2 axis is required for tumor-associated macrophages to promote colorectal cancer progression

机译:肿瘤相关巨噬细胞需要WNT5A / CAMKII / ERK / CCL2轴以促进结直肠癌进展

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Tumor-associated macrophages (TAMs) are closely correlated with tumor occurrence, invasion, and metastasis. However, factors affecting the biological functions of TAMs in colorectal cancer (CRC) are incompletely understood. Here, we found that Wnt5a was mainly expressed on TAMs of tumor stroma but not on CRC cells. Subsequently, we found that Wnt5asup+/sup TAMs facilitated tumor cell proliferation and migration, and recruited macrophages infiltration. Furthermore, Wnt5a knockdown impaired the pro-tumor roles of TAMs in vivo and in vitro. Mechanistically, the cancer-promoting roles of Wnt5a in TAMs depended on CaMKII-ERK pathway-mediated CCL2 secretion. Our data reveal the crucial role played by TAM-expressed Wnt5a in CRC tumorigenesis through paracrine secretion of CCL2. We first report the connection between Wnt5a/CaMKII/ERK/CCL2 axis and biological functions of TAMs in tumor microenvironment, indicating that Wnt5a may be a novel therapeutic target for CRC.? The author(s).
机译:肿瘤相关的巨噬细胞(TAMS)与肿瘤发生,侵袭和转移密切相关。然而,影响了影响结肠直肠癌(CRC)中TAMS的生物功能的因素被不完全理解。在这里,我们发现Wnt5a主要表达于肿瘤基质的TAM,但不在CRC细胞上表达。随后,我们发现Wnt5a + Tams促进肿瘤细胞增殖和迁移,并募集巨噬细胞浸润。此外,Wnt5a敲低损害了Tams在体内和体外的促肿瘤作用。机械地,WNT5a在TAMS中的癌症促进作用依赖于CAMKII-ERK途径介导的CCL2分泌。我们的数据揭示了通过CCL2的旁静脉分泌通过旁碱基分泌在CRC肿瘤发生中发挥的至关重要作用。我们首先报告Wnt5a / camkii / Erk / ccl2轴和肿瘤微环境中Tams的生物功能的连接,表明Wnt5a可以是CRC的新型治疗靶标。?作者。

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