Xing Lingling, Jiang Zhenyu, Xu Ruize, Dang Tong, Wu Jinbao, Chai Jianyuan, Meng Xianmei
Inner Mongolia Institute of Digestive Diseases, Baotou, China.
Inner Mongolia Engineering Research Center for Prevention and Treatment of Digestive Diseases, Baotou, China.
Sci Rep. 2025 Jan 13;15(1):1808. doi: 10.1038/s41598-025-86228-z.
CCN1 is a matricellular protein highly expressed in esophageal squamous cell carcinoma (ESCC) but hardly detectable in esophageal adenocarcinoma (EAC). Expression of CCN1 in EAC cells leads to TRAIL-mediated apoptosis. Unlike TRAIL, which primarily triggers cell death, APRIL and BAFF promote cell growth via NFκB signaling. They become active ligands by Furin cleavage. This study found that CCN1 upregulated APRIL and BAFF expression in both ESCC and EAC cells but attenuated their signaling in the latter. CCN1 kept Furin stable in ESCC allowing APRIL/BAFF to signal through their common receptor BCMA properly. In EAC cells, however, expression of CCN1 lowered Furin activity and thus limited APRIL/BAFF cleavage. As a result, ESCC cells benefited from CCN1 while EAC cell viability was attenuated by it.
CCN1是一种基质细胞蛋白,在食管鳞状细胞癌(ESCC)中高度表达,但在食管腺癌(EAC)中几乎检测不到。CCN1在EAC细胞中的表达导致TRAIL介导的细胞凋亡。与主要触发细胞死亡的TRAIL不同,APRIL和BAFF通过NFκB信号通路促进细胞生长。它们通过弗林蛋白酶切割成为活性配体。本研究发现,CCN1在ESCC和EAC细胞中均上调了APRIL和BAFF的表达,但在后者中减弱了它们的信号传导。CCN1在ESCC中使弗林蛋白酶保持稳定,从而使APRIL/BAFF能够通过它们的共同受体BCMA正常发出信号。然而,在EAC细胞中,CCN1的表达降低了弗林蛋白酶的活性,从而限制了APRIL/BAFF的切割。结果,ESCC细胞从CCN1中获益,而EAC细胞的活力则因CCN1而减弱。