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缺氧通过Rab11介导的整合素αvβ3/黏着斑激酶/磷脂酰肌醇-3激酶信号通路激活Rac1,刺激人宫颈癌细胞系HeLa/SiHa的侵袭和迁移。

Hypoxia stimulates invasion and migration of human cervical cancer cell lines HeLa/SiHa through the Rab11 trafficking of integrin αvβ3/FAK/PI3K pathway-mediated Rac1 activation.

作者信息

Xu Hao, Yuan Yuan, Wu Wenqian, Zhou Min, Jiang Qian, Niu Linjun, Ji Jiayin, Liu Nianli, Zhang Longzhen, Wang Xia

机构信息

Department of Radiotherapy, The Affiliated Hospital of Xuzhou Medical University, Xuzhou, China.

出版信息

J Biosci. 2017 Sep;42(3):491-499. doi: 10.1007/s12038-017-9699-0.

Abstract

Hypoxia plays a key role in tumour cell survival, invasion, and metastasis. An increasing number of studies have attempted to characterize the tumour response to hypoxia and to identify predictive markers of disease. Here we show that hypoxia increases tumour cell invasion and migration by the modulation of Rab11, an important molecule for vesicular trafficking. In our study, we found that Rab11, together with the activation of Rac1, could stimulate invasion and migration of cervical cancer cell lines HeLa/SiHa in hypoxia. Activation of Rac1 activity by hypoxia seems to be central to carcinoma invasion. We also found that these effects could be related to the integrin αvβ3. In addition, we studied the molecular pathway for this process. Our results showed that in cervical cancer cell lines HeLa/SiHa, Rac1 activation in hypoxia could stimulate invasion and migration, and this process was mediated by integrin αvβ3-mediated FAK and PI3K phosphorylation. Furthermore, hypoxia induced a dramatic increase in αvβ3 integrin surface expression, and this increase is dependent on Rab11. In conclusion, our study might provide a new mechanism for the effect of hypoxia on stimulating cervical carcinoma invasion.

摘要

缺氧在肿瘤细胞的存活、侵袭和转移中起关键作用。越来越多的研究试图描述肿瘤对缺氧的反应,并确定疾病的预测标志物。在此我们表明,缺氧通过调节Rab11(一种参与囊泡运输的重要分子)来增加肿瘤细胞的侵袭和迁移。在我们的研究中,我们发现Rab11与Rac1的激活一起,可在缺氧条件下刺激宫颈癌细胞系HeLa/SiHa的侵袭和迁移。缺氧对Rac1活性的激活似乎是癌症侵袭的关键。我们还发现这些效应可能与整合素αvβ3有关。此外,我们研究了这一过程的分子途径。我们的结果表明,在宫颈癌细胞系HeLa/SiHa中,缺氧条件下Rac1的激活可刺激侵袭和迁移,且这一过程由整合素αvβ3介导的FAK和PI3K磷酸化介导。此外,缺氧诱导αvβ3整合素表面表达显著增加,且这种增加依赖于Rab11。总之,我们的研究可能为缺氧刺激宫颈癌侵袭的作用提供一种新机制。

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