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• W2500530206 abstract "// Shun-Hong Huang 1 , Ching-Hsuan Law 1 , Ping-Hsueh Kuo 2 , Ren-Yu Hu 1 , Ching-Chieh Yang 3, 4 , Ting-Wen Chung 1 , Ji-Min Li 1 , Li-Hsun Lin 1 , Yi-Chung Liu 1, 12 , En-Chi Liao 1 , Yi-Ting Tsai 1 , Yu-Shan Wei 1 , Chi-Chen Lin 5, 6, 7, 8 , Chien-Wen Chang 9 , Hsiu-Chuan Chou 10 , Wen-Ching Wang 2 , Margaret Dah-Tsyr Chang 2 , Lu-Hai Wang 11 , Hsing-Jien Kung 11 , Hong-Lin Chan 1, 2 , Ping-Chiang Lyu 1, 2 1 Department of Medical Sciences and Institute of Bioinformatics and Structural Biology, National Tsing Hua University, Hsinchu, Taiwan 2 Department of Medical Sciences and Institute of Molecular and Cellular Biology, National Tsing Hua University, Hsinchu, Taiwan 3 Department of Radiation Oncology, Chi-Mei Medical Center, Tainan, Taiwan 4 Institute of Biomedical Sciences, National Sun Yat-Sen University, Kaohsiung, Taiwan 5 Institute of Biomedical Science, National Chung Hsing University, Taichung, Taiwan 6 Institute of Biomedical Science and Rong Hsing Research Center for Translational Medicine, National Chung Hsing University, Taichung, Taiwan 7 Department of Medical Research and Education, Taichung Veterans General Hospital, Taichung, Taiwan 8 Division of Chest Medicine. Department of Internal Medicine, Changhua Christian Hospital, Changhua, Taiwan 9 Department of Biomedical Engineering and Environmental Sciences, National Tsing Hua University, Taiwan 10 Department of Applied Science, National Hsinchu University of Education, Hsinchu, Taiwan 11 Institute of Molecular and Genomic Medicine, National Health Research Institutes, Miaoli County, Taiwan 12 Institute of Population Sciences, National Health Research Institutes, Miaoli County, Taiwan Correspondence to: Hong-Lin Chan, e-mail: hlchan@life.nthu.edu.tw Ping-Chiang Lyu, e-mail: pclyu@mx.nthu.edu.tw Keywords: ECM, EMT, IF, MMP-13, OSCC Received: November 23, 2015      Accepted: February 09, 2016      Published: March 06, 2016 ABSTRACT The oral cancer cell line OC3-I5 with a highly invasive ability was selected and derived from an established OSCC line OC3. In this study, we demonstrated that matrix metalloproteinases protein MMP-13 was up-regulated in OC3-I5 than in OC3 cells. We also observed that expression of epithelial–mesenchymal transition (EMT) markers including Twist, p-Src, Snail1, SIP1, JAM-A, and vinculin were increased in OC3-I5 compared to OC3 cells, whereas E-cadherin expression was decreased in the OC3-I5 cells. Using siMMP-13 knockdown techniques, we showed that siMMP-13 not only reduced the invasion and migration, but also the adhesion abilities of oral cancer cells. In support of the role of MMP-13 in metastasis, we used MMP-13 expressing plasmid-transfected 293T cells to enhance MMP-13 expression in the OC3 cells, transplanting the MMP-13 over expressing OC3 cells into nude mice led to enhanced lung metastasis. In summary, our findings show that MMP-13 promotes invasion and metastasis in oral cancer cells, suggesting altered expression of MMP-13 may be utilized to impede the process of metastasis." @default.
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• W2500530206 date "2016-07-25" @default.
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• W2500530206 title "Retraction: MMP-13 is involved in oral cancer cell metastasis" @default.
• W2500530206 doi "https://doi.org/10.18632/oncotarget.10823" @default.
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