Expression of ErbB Receptors and their Cognate Ligands in Gastric and Colon Cancer Cell Lines

被引:1
作者
Wu, William Ka Kei [1 ,2 ,3 ]
Tse, Timothy Tim Ming [1 ]
Sung, Joseph Jao Yiu [2 ,3 ]
Li, Zhi Jie [1 ]
Yu, Le [1 ]
Ch, Chi Hin [1 ,3 ]
机构
[1] Chinese Univ Hong Kong, Dept Pharmacol, Shatin, Hong Kong, Peoples R China
[2] Chinese Univ Hong Kong, Dept Med & Therapeut, Shatin, Hong Kong, Peoples R China
[3] Chinese Univ Hong Kong, Inst Digest Dis, Shatin, Hong Kong, Peoples R China
关键词
Gastric cancer; colon cancer; ErbB; neuroglycan-C; proliferation; GROWTH-FACTOR RECEPTOR; TYROSINE KINASE INHIBITORS; COLORECTAL-CANCER; BREAST-CANCER; NEUROGLYCAN-C; LUNG-CANCER; IN-VIVO; ACTIVATION; MECHANISMS; PROLIFERATION;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: ErbB receptors and their cognate ligands are implicated in cancer progression. Their expression in gastrointestinal cancer, however, has not been systemically studied. Materials and Methods: The expression of four ErbB receptors and a panel of ErbB ligands were determined by reverse transcription-PCR in two gastric (TMK1, MKN-45) and two colon (SW1116, HT-29) cancer cell lines. Cell proliferation was measured by MTT assay while gene knockdown was achieved by RNA interference. Results: ErbB1, ErbB2 and ErbB3 receptors and five known or putative ErbB ligands, namely, epiregulin, epidermal growth factor (EGF), heparin-binding EGF, transforming growth factor alpha (TGF alpha) and neuroglycan-C were expressed in all four cell lines. Knockdown of neuroglycan-C, however, did not affect cell proliferation. Conclusion: This study profiles the expression of ErbB receptors and their cognate ligands in gastric and colon cancer cells. These findings might lay the basis for the development of ErbB pathway-directed therapeutics for gastrointestinal cancer.
引用
收藏
页码:229 / 234
页数:6
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