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PAI-1 secreted from metastatic ovarian cancer cells triggers the tumor-promoting role of the mesothelium in a feedback loop to accelerate peritoneal dissemination

机译:从转移性卵巢癌细胞中分泌的pai-1触发了培养的肿瘤促进在反馈回路中以加速腹膜传播

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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 (NF kappa B) pathway in the CAMs, thus tran-scriptionally upregulating the expression of the downstream NF kappa B 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.
机译:由连续单层细胞覆盖的间皮是第一种免受转移性卵巢癌的保护屏障。然而,间皮细胞释放肿瘤促进因子,从而加速腹膜转移过程。我们鉴定了具有肿瘤促进潜力的癌症相关的间皮细胞(凸轮)。在这里,我们发现纤溶酶原激活剂抑制剂-1(PAI-1)诱导形成凸轮的形成,之后凸轮越来越多地分泌致癌素-8(IL-8)和CXC基序趋化因子配体5(CXCL5),进一步促进反馈回路中卵巢癌细胞转移。在形成凸轮之后,PAI-1在凸轮中激活核因子Kappa B(NF Kappa B)途径,从而进行扫描题目上游NFκB靶IL-8和CXCL5的表达。此外,PAI-1与卵巢癌患者的腹膜转移相关,并表明预后差。在离体和体内模型中,在敲击PAI-1表达后,卵巢癌细胞转移显着下降。因此,靶向PAI-1可以为未来的治疗方法提供潜在的目标,以防止在卵巢癌患者中形成凸轮和缓解腹膜转移。

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