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Then, the effects of <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\u201027 on the proliferation and apoptosis\u2010related molecules and angiogenesis in vitro of human umbilical vein endothelial cells (<jats:styled-content style=\"fixed-case\">HUVEC<\/jats:styled-content>s) were investigated. Finally, in vivo experiment was performed to further confirm the effects of IL\u201027.<\/jats:p><\/jats:sec><jats:sec><jats:title>Results<\/jats:title><jats:p>Compared with cervicitis, the cervical cancer tissues highly expressed <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\u201027. Both HeLa and CaSki cells secreted <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\u201027, and <jats:styled-content style=\"fixed-case\">HUVEC<\/jats:styled-content>s expressed low levels of <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\u201027 receptors (<jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\u201027R). However, the co\u2010culture of cervical cell lines and <jats:styled-content style=\"fixed-case\">HUVEC<\/jats:styled-content>s led to a significant elevation of <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\u201027R on <jats:styled-content style=\"fixed-case\">HUVEC<\/jats:styled-content>s. Co\u2010culturing with <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\u201027\u2010overexpressed HeLa cells downregulated Ki\u201067 and Bcl\u20102 and upregulated Fas expression in <jats:styled-content style=\"fixed-case\">HUVEC<\/jats:styled-content>s. In addition, overexpression of <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\u201027 in HeLa cells and CasKi cells secreted less <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\u20108 and could further restrict angiogenesis compared with control cells in vitro. In the subcutaneous tumorous model of C57\/<jats:styled-content style=\"fixed-case\">BL<\/jats:styled-content>6 mouse, there were decreased vessel density and tumor volume when inoculation with <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\u201027\u2010overexpressed <jats:styled-content style=\"fixed-case\">TC<\/jats:styled-content>\u20101 cells.<\/jats:p><\/jats:sec><jats:sec><jats:title>Conclusion<\/jats:title><jats:p>This study indicates that <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\u201027 secreted by cervical carcinoma cells restricts the angiogenesis in a paracrine manner in the pathogenesis of cervical cancer.<\/jats:p><\/jats:sec>","DOI":"10.1111\/aji.12706","type":"journal-article","created":{"date-parts":[[2017,5,16]],"date-time":"2017-05-16T04:06:42Z","timestamp":1494907602000},"source":"Crossref","is-referenced-by-count":8,"title":["The cross talk between cervical carcinoma cells and vascular endothelial cells mediated by 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