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http://ir.nhri.org.tw/handle/3990099045/4310
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Title: | Molecular characterization of invasive subpopulations from an esophageal squamous cell carcinoma cell line |
Authors: | Chen, YK;Chang, WSW;Wu, IC;Li, LH;Yang, SF;Chen, JYF;Hsu, MC;Cheni, SH;Wu, DC;Lee, JM;Huang, CH;Goan, YG;Chou, SH;Huang, CT;Wu, MT |
Contributors: | National Institute of Cancer Research |
Abstract: | Background: Once diagnosed, esophageal cancer has a very low overall 5-year survival rate. This study investigates the mechanisms behind the invasiveness and severity of esophageal squamous cell carcinoma (ESCC). Materials and Methods: Transwell invasion chamber was used to subdivide one Taiwanese ESCC cell line, CE81T/VGH, into sublines (CE81T-0, CE81T-1, CE81T-2, CE81T-3, and CE81T-4) in four rounds of assays; the most invasive were identified, and various factors related to their invasiveness measured. Results: CE81T-1, CE81T-2, CE81T-3 and CE81T-4 sublines were significantly more invasive than the parental cells (CE81T/VGH) and CE81T-0 subtitle. CE81T-1 and CE81T-4, the sublines we chose to study further, had significantly greater colony-forming ability (3.5- to 2.7-fold) and wound migrating activity (1.95- to 2.6-fold) than the parental cells in vitro (p<0.01). They also displayed greater tumorigenesis in immunodeficient BALB/c Foxlnn mice than the parental cells. We found an inverse correlation between expression of tissue inhibitor of metalloproteinase-2 and invasive ability, and a significant positive correlation between expressions of matrix metalloproteinase-1, vimentin, and p-Src (pY416) in these cell lines and their invasiveness (all p<0.05). Conclusion: The subline model may be used to study the molecular and genetic mechanisms underlying the invasion and metastasis of ESCC. |
Date: | 2010-03 |
Relation: | Anticancer Research. 2010 Mar;30(3):727-736. |
Link to: | http://ar.iiarjournals.org/content/30/3/727.abstract |
JIF/Ranking 2023: | http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=NHRI&SrcApp=NHRI_IR&KeyISSN=0250-7005&DestApp=IC2JCR |
Cited Times(WOS): | https://www.webofscience.com/wos/woscc/full-record/WOS:000276561300004 |
Cited Times(Scopus): | http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=77951035900 |
Appears in Collections: | [張文祥] 期刊論文
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