PCDH17 induces colorectal cancer metastasis by destroying the vascular endothelial barrier.

IF 8.1 1区 生物学 Q1 CELL BIOLOGY Cell Death & Disease Pub Date : 2025-01-21 DOI:10.1038/s41419-025-07355-z
Fengyun Dong, Pinghui Zhou, Feifei Kong, Sijie Cao, Xiaozao Pan, Shujing Cai, Xinke Chen, Sen Wang, Na Li, Baoyu He, Rou Zhao, Bin Zhang, Qingli Bie
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Abstract

Compromised vascular integrity facilitates the cancer cells extravasation and metastasis. However, the mechanisms leading to a disruption in vascular integrity in colorectal cancer (CRC) remain unclear. In this study, PCDH17 expression was higher in the vascular endothelial cells of colon cancer with distant metastasis, and the rates of PCDH17+ endothelial cells (ECs) was associated with the M stage in clinical pathological characteristics analysis and correlated with a poor survival prognosis. The liver and lung metastatic dissemination of MC-38 was significantly decreased in PCDH17-/-mice. The ubiquitination and degradation of VEGFR2 was prevented by the interaction between PCDH17 and the E3 ubiquitin ligase MARCH5, which causing the separation of internalized VE-cadherin, and increased the vascular permeability and metastasis of CRC. These results highlight the importance of PCDH17 in maintaining vascular integrity, which has emphasis for endothelial barrier function in metastatic cancer. PCDH17 has the potential to be a marker for predicting tumor metastasis as well as a viable treatment target for CRC.

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PCDH17通过破坏血管内皮屏障诱导结直肠癌转移。
血管完整性受损有利于癌细胞外渗和转移。然而,导致结直肠癌(CRC)血管完整性破坏的机制尚不清楚。本研究中,PCDH17在远处转移结肠癌血管内皮细胞中表达较高,且PCDH17+内皮细胞(ECs)的比例与临床病理特征分析中的M期相关,且与生存预后差相关。MC-38在PCDH17-/-小鼠的肝脏和肺转移性播散明显减少。PCDH17与E3泛素连接酶MARCH5相互作用,阻止VEGFR2泛素化降解,导致内化VE-cadherin分离,增加结直肠癌的血管通透性和转移。这些结果强调了PCDH17在维持血管完整性方面的重要性,特别是在转移性癌症中内皮屏障功能。PCDH17有可能成为预测肿瘤转移的标志物,也可能成为结直肠癌的可行治疗靶点。
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来源期刊
Cell Death & Disease
Cell Death & Disease CELL BIOLOGY-
CiteScore
15.10
自引率
2.20%
发文量
935
审稿时长
2 months
期刊介绍: Brought to readers by the editorial team of Cell Death & Differentiation, Cell Death & Disease is an online peer-reviewed journal specializing in translational cell death research. It covers a wide range of topics in experimental and internal medicine, including cancer, immunity, neuroscience, and now cancer metabolism. Cell Death & Disease seeks to encompass the breadth of translational implications of cell death, and topics of particular concentration will include, but are not limited to, the following: Experimental medicine Cancer Immunity Internal medicine Neuroscience Cancer metabolism
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