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Liu, Ling-Zhi [Verfasser:in]; Ge, Xin [Verfasser:in]; He, Jun [Verfasser:in]; Wang, Lin [Verfasser:in]; Zhao, Lei [Verfasser:in]; Wang, Yifang [Verfasser:in]; Wu, Gang [Verfasser:in]; Shu, Yongqian [Verfasser:in]; Gong, Wei [Verfasser:in]; Ma, Xin-Liang [Verfasser:in]; Wang, Yajing [Verfasser:in]; Jiang, Bing-Hua [Verfasser:in]

Epigenetic Alterations of Cxcl5 in Cr(Vi)-Induced Carcinogenesis

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  • Medientyp: E-Book
  • Titel: Epigenetic Alterations of Cxcl5 in Cr(Vi)-Induced Carcinogenesis
  • Beteiligte: Liu, Ling-Zhi [Verfasser:in]; Ge, Xin [Verfasser:in]; He, Jun [Verfasser:in]; Wang, Lin [Verfasser:in]; Zhao, Lei [Verfasser:in]; Wang, Yifang [Verfasser:in]; Wu, Gang [Verfasser:in]; Shu, Yongqian [Verfasser:in]; Gong, Wei [Verfasser:in]; Ma, Xin-Liang [Verfasser:in]; Wang, Yajing [Verfasser:in]; Jiang, Bing-Hua [Verfasser:in]
  • Erschienen: [S.l.]: SSRN, [2022]
  • Umfang: 1 Online-Ressource (29 p)
  • Sprache: Englisch
  • DOI: 10.2139/ssrn.4034516
  • Identifikator:
  • Entstehung:
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  • Beschreibung: Chronic exposure to hexavalent chromium compounds [Cr(VI)] is associated with an increased risk of cancers, but the molecular mechanisms remain to be elucidated. In this study, we found that CXCL5 levels in peripheral blood monocytes (PBMCs) and plasma from workers with occupational exposure to Cr(VI) were dramatically upregulated compared to non-exposure healthy subjects, and plasma C-X-C Motif Chemokine Ligand 5 (CXCL5) CXCL5 levels were positively correlated with Cr concentrations in subjects’ toenails. Zinc chromate exposed mice showed higher levels of CXCL5 and its receptor CXCR2 in lung tissues, and in PBMCs. Similar CXCL5 upregulation was evident in Cr(VI)-induced transformed (Cr-T) cells with long-term Cr(VI) treatment. Mechanistic studies showed that elevated CXCL5 expression levels were regulated by Cr(VI)-induced histone modifications and DNA hypomethylation, and that the c-Myc/p300 complex was a key upstream regulator of histone H3 acetylation. CXCL5 overexpression promoted Cr(VI)-induced the epithelial to mesenchyme transition (EMT) by upregulating zinc finger E-box binding homeobox 1 (ZEB1) to promote tumor development. Our findings identify a novel mechanism by which CXCL5 is upregulated and promotes EMT and carcinogenesis upon chronic Cr(VI) exposure. Our work also implies that CXCL5 mRNA and protein levels will elevate in PBMCs and serum after occupational Cr(VI) exposure, which may be a potential target and biomarker for cancer prevention and health surveillance among populations exposed to Cr(VI)
  • Zugangsstatus: Freier Zugang