I‐branching N‐acetylglucosaminyltransferase regulates prostate cancer invasiveness by enhancing α5β1 integrin signaling. Issue 3 (10th February 2016)
- Record Type:
- Journal Article
- Title:
- I‐branching N‐acetylglucosaminyltransferase regulates prostate cancer invasiveness by enhancing α5β1 integrin signaling. Issue 3 (10th February 2016)
- Main Title:
- I‐branching N‐acetylglucosaminyltransferase regulates prostate cancer invasiveness by enhancing α5β1 integrin signaling
- Authors:
- Mikami, Jotaro
Tobisawa, Yuki
Yoneyama, Tohru
Hatakeyama, Shingo
Mori, Kazuyuki
Hashimoto, Yasuhiro
Koie, Takuya
Ohyama, Chikara
Fukuda, Minoru - Abstract:
- Abstract : Cell surface carbohydrates are important for cell migration and invasion of prostate cancer (PCa). Accordingly, the I‐branching N ‐acetylglucosaminyltransferase (GCNT2) converts linear i‐antigen to I‐branching glycan, and its expression is associated with breast cancer progression. In the present study, we identified relationships between GCNT2 expression and clinicopathological parameters in patients with PCa. Paraffin‐embedded PCa specimens were immunohistochemically tested for GCNT2 expression, and the roles of GCNT2 in PCa progression were investigated using cell lines with high GCNT2 expression and low GCNT2 expression. GCNT2‐positive cells were significantly lesser in organ‐confined disease than in that with extra‐capsular extensions, and GCNT2‐negative tumors were associated with significantly better prostate‐specific antigen‐free survival compared with GCNT2‐positive tumors. Subsequent functional studies revealed that knockdown of GCNT2 expression in PCa cell lines significantly inhibited cell migration and invasion. GCNT2 regulated the expression of cell surface I‐antigen on the O ‐glycan and glycolipid. Moreover, I‐antigen‐bearing glycolipids were subject to α5β1 integrin–fibronectin mediated protein kinase B phosphorylation. In conclusion, GCNT2 expression is closely associated with invasive potential of PCa. Abstract : The I‐branching N ‐acetylglucosaminyltransferase (GCNT2) is a glycosyltransferase that converts linear i‐antigens to I‐branchingAbstract : Cell surface carbohydrates are important for cell migration and invasion of prostate cancer (PCa). Accordingly, the I‐branching N ‐acetylglucosaminyltransferase (GCNT2) converts linear i‐antigen to I‐branching glycan, and its expression is associated with breast cancer progression. In the present study, we identified relationships between GCNT2 expression and clinicopathological parameters in patients with PCa. Paraffin‐embedded PCa specimens were immunohistochemically tested for GCNT2 expression, and the roles of GCNT2 in PCa progression were investigated using cell lines with high GCNT2 expression and low GCNT2 expression. GCNT2‐positive cells were significantly lesser in organ‐confined disease than in that with extra‐capsular extensions, and GCNT2‐negative tumors were associated with significantly better prostate‐specific antigen‐free survival compared with GCNT2‐positive tumors. Subsequent functional studies revealed that knockdown of GCNT2 expression in PCa cell lines significantly inhibited cell migration and invasion. GCNT2 regulated the expression of cell surface I‐antigen on the O ‐glycan and glycolipid. Moreover, I‐antigen‐bearing glycolipids were subject to α5β1 integrin–fibronectin mediated protein kinase B phosphorylation. In conclusion, GCNT2 expression is closely associated with invasive potential of PCa. Abstract : The I‐branching N ‐acetylglucosaminyltransferase (GCNT2) is a glycosyltransferase that converts linear i‐antigens to I‐branching glycans. In the present study, we demonstrated that GCNT2 expression correlates with malignant potential of prostate cancer (PCa). GCNT2‐expressing PCa formed I‐branching glycan on cell surface glycolipids, and GCNT2‐low PCa cells exhibited decreased invasion potential and α5β1 integrin‐mediated protein kinase B phosphorylation, suggesting that GCNT2 plays important roles in PCa invasiveness. … (more)
- Is Part Of:
- Cancer science. Volume 107:Issue 3(2016)
- Journal:
- Cancer science
- Issue:
- Volume 107:Issue 3(2016)
- Issue Display:
- Volume 107, Issue 3 (2016)
- Year:
- 2016
- Volume:
- 107
- Issue:
- 3
- Issue Sort Value:
- 2016-0107-0003-0000
- Page Start:
- 359
- Page End:
- 368
- Publication Date:
- 2016-02-10
- Subjects:
- Cell migration -- glycolipid -- I‐antigen -- I‐branching N‐acetylglucosaminyltransferase -- prostate cancer
Cancer -- Periodicals
Neoplasms -- Periodicals
Research -- Periodicals
Electronic journals
616.994005 - Journal URLs:
- http://firstsearch.oclc.org ↗
http://firstsearch.oclc.org/journal=1347-9032;screen=info;ECOIP ↗
http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1349-7006 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/cas.12859 ↗
- Languages:
- English
- ISSNs:
- 1347-9032
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3046.603000
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