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Jul 15, 2004 (publication date) through Apr 25, 2024
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Publication Name
World Journal of Gastroenterology
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1007-9327
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Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA
| For: | Si SH, Yang JM, Peng ZH, Luo YH, Zhou P. Effects of KAI1 gene on growth and invasion of human hepatocellular carcinoma MHCC97-H cells. World J Gastroenterol 2004; 10(14): 2019-2023 [PMID: 15237426 DOI: 10.3748/wjg.v10.i14.2019] |
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| URL: | https://www.wjgnet.com/1007-9327/full/v10/i14/2019.htm |
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C.K. Miranti. Controlling cell surface dynamics and signaling: How CD82/KAI1 suppresses metastasis. Cellular Signalling 2009; 21(2): 196 doi: 10.1016/j.cellsig.2008.08.023
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Shuo Wang, Jiang Chen, Xiao-Zhong Guo. <i>KAI1/CD82</i> gene and autotaxin-lysophosphatidic acid axis in gastrointestinal cancers. World Journal of Gastrointestinal Oncology 2022; 14(8): 1388-1405 doi: 10.4251/wjgo.v14.i8.1388
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Sina Upheber, Alexandra Karle, Julia Miller, Stephanie Schlaugk, Eva Gross, Ute Reuning. Alternative splicing of KAI1 abrogates its tumor-suppressive effects on integrin αvβ3-mediated ovarian cancer biology. Cellular Signalling 2015; 27(3): 652 doi: 10.1016/j.cellsig.2014.11.028
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Jian‐min Yang, Zhi‐hong Peng, Sui‐hai Si, Wei‐wen Liu, Yuan‐hui Luo, Zai‐yuan Ye. KAI1 gene suppresses invasion and metastasis of hepatocellular carcinoma MHCC97‐H cells in vitro and in animal models. Liver International 2008; 28(1): 132 doi: 10.1111/j.1478-3231.2007.01620.x
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Hyun-Ah Lee, Iha Park, Hee-Jung Byun, Dooil Jeoung, Young-Myeong Kim, Hansoo Lee. Metastasis Suppressor KAI1/CD82 Attenuates the Matrix Adhesion of Human Prostate Cancer Cells by Suppressing Fibronectin Expression and β <sub>1</sub> Integrin Activation. Cellular Physiology and Biochemistry 2011; 27(5): 575 doi: 10.1159/000329979
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Y Suh, C-H Yoon, R-K Kim, E-J Lim, Y S Oh, S-G Hwang, S An, G Yoon, M C Gye, J-M Yi, M-J Kim, S-J Lee. Claudin-1 induces epithelial–mesenchymal transition through activation of the c-Abl-ERK signaling pathway in human liver cells. Oncogene 2013; 32(41): 4873 doi: 10.1038/onc.2012.505
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