Mechanisms of confluence-dependent expression of CD26 in colon cancer cell lines
<p>Abstract</p> <p>Background</p> <p>CD26 (dipeptidyl peptidase IV, DPPIV) is a 110 kDa surface glycoprotein expressed in most normal tissues, and is a potential novel therapeutic target for selected cancers. Our work evaluates the mechanism involved in confluence-depen...
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doaj-e56fc07b26f14a99bfa6a0cf6674158a2020-11-25T00:19:21ZengBMCBMC Cancer1471-24072011-02-011115110.1186/1471-2407-11-51Mechanisms of confluence-dependent expression of CD26 in colon cancer cell linesMorimoto ChikaoOhnuma KeiUrasaki YasuyoHavre Pamela AAbe MasakoDang Long HDang Nam H<p>Abstract</p> <p>Background</p> <p>CD26 (dipeptidyl peptidase IV, DPPIV) is a 110 kDa surface glycoprotein expressed in most normal tissues, and is a potential novel therapeutic target for selected cancers. Our work evaluates the mechanism involved in confluence-dependent CD26 expression in colon cancer.</p> <p>Methods</p> <p>Colon adenocarcinoma cells were grown to confluence, and expression of CD26 and transcription factors implicated in its regulation was confirmed by immunofluorescence and Western blotting. Real-time PCR was also performed to evaluate CD26 upregulation at the transcriptional level. The influence of c-Myc on CD26 expression during different growth conditions was further evaluated following transient transfection of a c-Myc-expressing plasmid and a c-Myc specific siRNA.</p> <p>Results</p> <p>We found that the colon cancer cell lines HCT-116 and HCT-15 exhibited a confluence-dependent increase in CD26 mRNA and protein, associated with decreased expression of c-Myc, increased USF-1 and Cdx 2 levels, and unchanged HNF-1α expression. Meanwhile, ectopic expression of c-Myc in both cell lines led to decreased CD26 expression. In contrast, transfection of a siRNA targeted to Cdx2 resulted in decreased CD26 level. Importantly, culturing of cells in serum-depleted media, but not acidic conditions, upregulated CD26. While HIF-1α level also increased when cells were cultured in serum-depleted media, its expression was required but not sufficient for CD26 upregulation.</p> <p>Conclusions</p> <p>CD26 mRNA and protein levels increase in a confluence-dependent manner in colon carcinoma cell lines, with c-Myc acting as a repressor and Cdx2 acting as an enhancer of CD26 expression. The enhanced expression of CD26 in serum-depleted media and a requirement for HIF-1α suggest a role for nutrients or growth factors in the regulation of CD26 protein expression.</p> http://www.biomedcentral.com/1471-2407/11/51 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Morimoto Chikao Ohnuma Kei Urasaki Yasuyo Havre Pamela A Abe Masako Dang Long H Dang Nam H |
spellingShingle |
Morimoto Chikao Ohnuma Kei Urasaki Yasuyo Havre Pamela A Abe Masako Dang Long H Dang Nam H Mechanisms of confluence-dependent expression of CD26 in colon cancer cell lines BMC Cancer |
author_facet |
Morimoto Chikao Ohnuma Kei Urasaki Yasuyo Havre Pamela A Abe Masako Dang Long H Dang Nam H |
author_sort |
Morimoto Chikao |
title |
Mechanisms of confluence-dependent expression of CD26 in colon cancer cell lines |
title_short |
Mechanisms of confluence-dependent expression of CD26 in colon cancer cell lines |
title_full |
Mechanisms of confluence-dependent expression of CD26 in colon cancer cell lines |
title_fullStr |
Mechanisms of confluence-dependent expression of CD26 in colon cancer cell lines |
title_full_unstemmed |
Mechanisms of confluence-dependent expression of CD26 in colon cancer cell lines |
title_sort |
mechanisms of confluence-dependent expression of cd26 in colon cancer cell lines |
publisher |
BMC |
series |
BMC Cancer |
issn |
1471-2407 |
publishDate |
2011-02-01 |
description |
<p>Abstract</p> <p>Background</p> <p>CD26 (dipeptidyl peptidase IV, DPPIV) is a 110 kDa surface glycoprotein expressed in most normal tissues, and is a potential novel therapeutic target for selected cancers. Our work evaluates the mechanism involved in confluence-dependent CD26 expression in colon cancer.</p> <p>Methods</p> <p>Colon adenocarcinoma cells were grown to confluence, and expression of CD26 and transcription factors implicated in its regulation was confirmed by immunofluorescence and Western blotting. Real-time PCR was also performed to evaluate CD26 upregulation at the transcriptional level. The influence of c-Myc on CD26 expression during different growth conditions was further evaluated following transient transfection of a c-Myc-expressing plasmid and a c-Myc specific siRNA.</p> <p>Results</p> <p>We found that the colon cancer cell lines HCT-116 and HCT-15 exhibited a confluence-dependent increase in CD26 mRNA and protein, associated with decreased expression of c-Myc, increased USF-1 and Cdx 2 levels, and unchanged HNF-1α expression. Meanwhile, ectopic expression of c-Myc in both cell lines led to decreased CD26 expression. In contrast, transfection of a siRNA targeted to Cdx2 resulted in decreased CD26 level. Importantly, culturing of cells in serum-depleted media, but not acidic conditions, upregulated CD26. While HIF-1α level also increased when cells were cultured in serum-depleted media, its expression was required but not sufficient for CD26 upregulation.</p> <p>Conclusions</p> <p>CD26 mRNA and protein levels increase in a confluence-dependent manner in colon carcinoma cell lines, with c-Myc acting as a repressor and Cdx2 acting as an enhancer of CD26 expression. The enhanced expression of CD26 in serum-depleted media and a requirement for HIF-1α suggest a role for nutrients or growth factors in the regulation of CD26 protein expression.</p> |
url |
http://www.biomedcentral.com/1471-2407/11/51 |
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