间皮
卵巢癌
转移
间皮细胞
癌症研究
CXCL5型
离体
趋化因子
卵巢肿瘤
医学
体内
癌症
生物
癌细胞
病理
内科学
受体
生物技术
作者
Yang Peng,Hiroaki Kajiyama,Hong Yuan,Kae Nakamura,Masato Yoshihara,Akira Yokoi,Kayo Fujikake,Hiroaki Yasui,Nobuhisa Yoshikawa,Shiro Suzuki,Takeshi Senga,Kiyosumi Shibata,Fumitaka Kikkawa
标识
DOI:10.1016/j.canlet.2018.10.027
摘要
The mesothelium, covered by a continuous monolayer of mesothelial cells, is the first protective barrier against metastatic ovarian cancer. However, mesothelial cells release tumor-promoting factors that accelerate the process of peritoneal metastasis. We identified cancer-associated mesothelial cells (CAMs) that had tumor-promoting potential. Here, we found that plasminogen activator inhibitor-1 (PAI-1) induced the formation of CAMs, after which CAMs increasingly secreted the oncogenic factors interleukin-8 (IL-8) and C-X-C motif chemokine ligand 5 (CXCL5), further promoting the metastasis of ovarian cancer cells in a feedback loop. After the formation of CAMs, PAI-1 activated the nuclear factor kappa B (NFκB) pathway in the CAMs, thus transcriptionally upregulating the expression of the downstream NFκB targets IL-8 and CXCL5. Moreover, PAI-1 correlated with peritoneal metastasis in ovarian cancer patients and indicated a poor prognosis. In both ex vivo and in vivo models, after PAI-1 expression was knocked down, the metastasis of ovarian cancer cells decreased significantly. Therefore, targeting PAI-1 may provide a potential target for future therapeutics to prevent the formation of CAMs and alleviate peritoneal metastasis in ovarian cancer patients.
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