Transformation-associated gene regulation by ATF6alpha during hepatocarcinogenesis

• Published in: FEBS letters Vol. 580; no. 1; pp. 184 - 190
• Main Authors: Arai, Masaaki, Kondoh, Nobuo, Imazeki, Nobuo, Hada, Akiyuki, Hatsuse, Kazuo, Kimura, Fumihiro, Matsubara, Osamu, Mori, Kazutoshi, Wakatsuki, Toru, Yamamoto, Mikio
• Format: Journal Article
• Language: English
• Published: England 09.01.2006
• Subjects: Activating Transcription Factor 6 - genetics; Activating Transcription Factor 6 - metabolism; Carcinoma - genetics; Carcinoma - metabolism; Carcinoma - pathology; Cell Line, Tumor; Cell Transformation, Neoplastic - genetics; Cell Transformation, Neoplastic - metabolism; Endoplasmic Reticulum - genetics; Endoplasmic Reticulum - metabolism; Gene Expression Regulation, Neoplastic; Humans; Liver Neoplasms - genetics; Liver Neoplasms - metabolism; Liver Neoplasms - pathology; Neoplasm Proteins - biosynthesis; Neoplasm Proteins - genetics; Regulatory Elements, Transcriptional - genetics
• ISSN: 0014-5793

We have previously reported that the endoplasmic reticulum (ER) stress-regulated transmembrane transcription factor 6 alpha (ATF6alpha) is implicated in the pathogenesis of hepatocellular carcinomas (HCCs). In order to further identify genes that are regulated by ATF6alpha, the global gene expression profiles of the ATF6alpha-transfected and untransfected HCC cell line, HLF, were analyzed. These results were then compared with the differential gene expression patterns of poorly differentiated HCC and control non-tumorous liver tissue. Our findings demonstrate that at least 18 genes are specifically upregulated by ATF6alpha, while another UPR mediator, XBP1 or ER-stress inducer, thapsigargin could partially stimulate or even repress some of them in HCC cells. Moreover, six of these identified genes contain potential ER stress-responsive elements and/or unfolded protein response elements in their 5' regulatory regions.