CXCL3 overexpression promotes the tumorigenic potential of uterine cervical cancer cells via the MAPK/ERK pathway
Autor: | Weiqun Wang, Bai-Xin Wang, Yaling Qi, Hui Zhang, Hongyu Sui, Yue Li, Xia-Xia Man, Pengxia Zhang, Chunbin Zhang, Xiao-Lian Zhao, Lin-Lin Jia, Haiyan Luan, Jing Li, Shu-Fang Qi, Xiu-Sheng Qu |
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Rok vydání: | 2019 |
Předmět: |
0301 basic medicine
MAPK/ERK pathway Adult Chemokine Chemokine CXCL5 Physiology Clinical Biochemistry Mice Nude Uterine Cervical Neoplasms Apoptosis HeLa 03 medical and health sciences 0302 clinical medicine Cell Movement Paracrine Communication Animals Humans Neoplasm Invasiveness Extracellular Signal-Regulated MAP Kinases Aged Cell Proliferation bcl-2-Associated X Protein biology Kinase Chemistry Cell Biology Middle Aged biology.organism_classification Up-Regulation Gene Expression Regulation Neoplastic 030104 developmental biology CXCL3 Proto-Oncogene Proteins c-bcl-2 CXCL5 Cell culture 030220 oncology & carcinogenesis Cancer research biology.protein Female Signal transduction Chemokines CXC HeLa Cells Signal Transduction |
Zdroj: | Journal of cellular physiologyREFERENCES. 235(5) |
ISSN: | 1097-4652 |
Popis: | CXCL3 belongs to the CXC-type chemokine family and is known to play a multifaceted role in various human malignancies. While its clinical significance and mechanisms of action in uterine cervical cancer (UCC) remain unclear. This investigation demonstrated that the UCC cell line HeLa expressed CXCL3, and strong expression of CXCL3 was detected in UCC tissues relative to nontumor tissues. In addition, CXCL3 expression was strongly correlated with CXCL5 expression in UCC tissues. In vitro, HeLa cells overexpressing CXCL3, HeLa cells treated with exogenous CXCL3 or treated with conditioned medium from WPMY cells overexpressing CXCL3, exhibited enhanced proliferation and migration activities. In agreement with these findings, CXCL3 overexpression was also associated with the generation of HeLa cell tumor xenografts in athymic nude mice. Subsequent mechanistic studies demonstrated that CXCL3 overexpressing influenced the expression of extracellular signal-regulated kinase (ERK) signaling pathway associated genes, including ERK1/2, Bcl-2, and Bax, whereas the CXCL3-induced proliferation and migration effects were attenuated by exogenous administration of the ERK1/2 blocker PD98059. The data of the current investigation support that CXCL3 appears to hold promise as a potential tumor marker and interference target for UCC. |
Databáze: | OpenAIRE |
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