Epithelial to mesenchymal transition might be induced via CD44 isoform switching in colorectal cancer. Issue 6 (29th June 2014)
- Record Type:
- Journal Article
- Title:
- Epithelial to mesenchymal transition might be induced via CD44 isoform switching in colorectal cancer. Issue 6 (29th June 2014)
- Main Title:
- Epithelial to mesenchymal transition might be induced via CD44 isoform switching in colorectal cancer
- Authors:
- Mashita, Naoki
Yamada, Suguru
Nakayama, Goro
Tanaka, Chie
Iwata, Naoki
Kanda, Mitsuro
Kobayashi, Daisuke
Fujii, Tsutomu
Sugimoto, Hiroyuki
Koike, Masahiko
Nomoto, Shuji
Fujiwara, Michitaka
Kodera, Yasuhiro - Abstract:
- <abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="jso23705-sec-0001" sec-type="section"> <title>Background</title> <p>Isoform switching of CD44 is associated with epithelial to mesenchymal transition (EMT) in several cancers; however, the clinical implications of this remain unclear for colorectal cancer (CRC).</p> </sec> <sec id="jso23705-sec-0002" sec-type="section"> <title>Methods</title> <p>We measured expression levels of E‐cadherin, vimentin, CD44 standard (CD44s) and CD44 variant 9 (CD44v9) transcripts in 14 CRC cell lines and 150 CRC patients. We determined EMT and CD44 status by calculating vimentin/E‐cadherin and CD44s/CD44v9 expression ratios, respectively. Associations between EMT status and CD44 isoform switching, and between clinicopathological factors and prognosis were analyzed.</p> </sec> <sec id="jso23705-sec-0003" sec-type="section"> <title>Results</title> <p>CD44s was highly expressed in mesenchymal‐type cell lines, while CD44v9 was highly expressed in epithelial‐type cell lines. CD44 knockdown resulted in decreased levels of vimentin expression, and significantly reduced proliferation, migration and invasion of cells. In CRC patients, the mesenchymal group and the high CD44 status group exhibited significantly poorer survival than that for the epithelial group (5‐year survival; 62.1% vs. 85.5%, <italic>P</italic> = 0.0085) and the low CD44 status group (5‐year survival; 66.1% vs. 85.0%,<abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="jso23705-sec-0001" sec-type="section"> <title>Background</title> <p>Isoform switching of CD44 is associated with epithelial to mesenchymal transition (EMT) in several cancers; however, the clinical implications of this remain unclear for colorectal cancer (CRC).</p> </sec> <sec id="jso23705-sec-0002" sec-type="section"> <title>Methods</title> <p>We measured expression levels of E‐cadherin, vimentin, CD44 standard (CD44s) and CD44 variant 9 (CD44v9) transcripts in 14 CRC cell lines and 150 CRC patients. We determined EMT and CD44 status by calculating vimentin/E‐cadherin and CD44s/CD44v9 expression ratios, respectively. Associations between EMT status and CD44 isoform switching, and between clinicopathological factors and prognosis were analyzed.</p> </sec> <sec id="jso23705-sec-0003" sec-type="section"> <title>Results</title> <p>CD44s was highly expressed in mesenchymal‐type cell lines, while CD44v9 was highly expressed in epithelial‐type cell lines. CD44 knockdown resulted in decreased levels of vimentin expression, and significantly reduced proliferation, migration and invasion of cells. In CRC patients, the mesenchymal group and the high CD44 status group exhibited significantly poorer survival than that for the epithelial group (5‐year survival; 62.1% vs. 85.5%, <italic>P</italic> = 0.0085) and the low CD44 status group (5‐year survival; 66.1% vs. 85.0%, <italic>P</italic> = 0.0251). On multivariate analysis, CD44 status was an independent prognostic factor.</p> </sec> <sec id="jso23705-sec-0004" sec-type="section"> <title>Conclusions</title> <p>The status of EMT and CD44 is a critical prognostic factor, with CD44 isoform switching a possible trigger for EMT in CRC. <italic>J. Surg. Oncol. 2014 110:745–751</italic>. © 2014 Wiley Periodicals, Inc.</p> </sec> </abstract> … (more)
- Is Part Of:
- Journal of surgical oncology. Volume 110:Issue 6(2014:Nov. 01)
- Journal:
- Journal of surgical oncology
- Issue:
- Volume 110:Issue 6(2014:Nov. 01)
- Issue Display:
- Volume 110, Issue 6 (2014)
- Year:
- 2014
- Volume:
- 110
- Issue:
- 6
- Issue Sort Value:
- 2014-0110-0006-0000
- Page Start:
- 745
- Page End:
- 751
- Publication Date:
- 2014-06-29
- Subjects:
- Cancer -- Surgery -- Periodicals
Neoplasms -- Periodicals
616 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1096-9098 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/jso.23705 ↗
- Languages:
- English
- ISSNs:
- 0022-4790
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5067.380000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 3140.xml