Literature DB >> 19331154

Expression of ErbB receptors and their cognate ligands in gastric and colon cancer cell lines.

William Ka Kei Wu1, Timothy Tim Ming Tse, Joseph Jao Yiu Sung, Zhi Jie Li, Le Yu, Chi Hin Cho.   

Abstract

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 (TGFalpha) 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.

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Year:  2009        PMID: 19331154

Source DB:  PubMed          Journal:  Anticancer Res        ISSN: 0250-7005            Impact factor:   2.480


  18 in total

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4.  Integrated Proteomic and Genomic Analysis of Gastric Cancer Patient Tissues.

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8.  Tumor endothelial cells promote metastasis and cancer stem cell-like phenotype through elevated Epiregulin in esophageal cancer.

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9.  Autocrine-derived epidermal growth factor receptor ligands contribute to recruitment of tumor-associated macrophage and growth of basal breast cancer cells in vivo.

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10.  Simultaneous profiling of 194 distinct receptor transcripts in human cells.

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Journal:  Sci Signal       Date:  2013-08-06       Impact factor: 8.192

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