Inner Mongolia Institute of Digestive Diseases, Inner Mongolia Engineering Research Center for Prevention and Treatment of Digestive Diseases, Inner Mongolia University of Science and Technology, 74506The Second Affiliated Hospital of Baotou Medical College, Baotou, China.
Laboratory of Gastrointestinal Injury and Cancer, VA Long Beach Healthcare System, Long Beach, CA, USA.
Cancer Control. 2022 Jan-Dec;29:10732748221074734. doi: 10.1177/10732748221074734.
: Esophageal cancer is one of the most common and deadliest cancers in the world, particularly esophageal adenocarcinoma. There has never been a special drug to treat it.: This article summarizes the work that we have done in our laboratory about the role of CCN1 in esophageal cancer and gives a new perspective of CCN1 biology.: This is a review article. : The work was done using validated cell lines and fixed human tissue slides.: This is a review article, therefore, no data collection or analysis was involved.: CCN1 is a matricellular protein supporting adhesion, migration, and survival in normal cells, but in the esophageal cancer cells, it induces TRAIL-mediated apoptosis. CCN1 promotes TRAIL and its death receptor expression but downregulates the decoy receptors and survivin in a p53-dependant manner. It was thought that CCN1 relies on TNF to induce apoptosis, but our study found that these two molecules antagonize each other. CCN1 promotes TNFR1 cleavage and uses the soluble product to block TNF signaling, while TNF upregulates PGLYRP1 to overcome this obstacle because PGLYRP1 is a secreted protein that competes with TNF for TNFR1 binding. As a result, when CCN1 and TNF are present together in the vicinity of esophageal tumors, they cancel each other out.: Based on our laboratory study, CCN1 has much potential to be a candidate for the treatment of esophageal cancer.
食管癌是世界上最常见和最致命的癌症之一,特别是食管腺癌。目前还没有专门用于治疗它的药物。本文总结了我们实验室在 CCN1 与食管癌关系方面的工作,为 CCN1 生物学提供了新的视角。这是一篇综述文章。工作使用了经过验证的细胞系和固定的人类组织切片。这是一篇综述文章,因此不涉及数据收集或分析。CCN1 是一种基质细胞蛋白,在正常细胞中支持黏附、迁移和存活,但在食管癌细胞中,它诱导 TRAIL 介导的细胞凋亡。CCN1 以依赖 p53 的方式促进 TRAIL 和其死亡受体的表达,但下调诱饵受体和生存素。人们认为 CCN1 依赖 TNF 诱导细胞凋亡,但我们的研究发现这两种分子相互拮抗。CCN1 促进 TNFR1 切割,并利用可溶性产物阻断 TNF 信号,而 TNF 上调 PGLYRP1 以克服这一障碍,因为 PGLYRP1 是一种分泌蛋白,与 TNF 竞争 TNFR1 结合。因此,当 CCN1 和 TNF 同时存在于食管肿瘤附近时,它们会相互抵消。基于我们实验室的研究,CCN1 很有潜力成为治疗食管癌的候选药物。