Podoplanin is expressed at the invasive front of esophageal squamous cell carcinomas and is involved in collective cell invasion. Issue 12 (22nd October 2013)
- Record Type:
- Journal Article
- Title:
- Podoplanin is expressed at the invasive front of esophageal squamous cell carcinomas and is involved in collective cell invasion. Issue 12 (22nd October 2013)
- Main Title:
- Podoplanin is expressed at the invasive front of esophageal squamous cell carcinomas and is involved in collective cell invasion
- Authors:
- Nakashima, Yuichiro
Yoshinaga, Keiji
Kitao, Hiroyuki
Ando, Koji
Kimura, Yasue
Saeki, Hiroshi
Oki, Eiji
Morita, Masaru
Kakeji, Yoshihiro
Hirahashi, Minako
Oda, Yoshinao
Maehara, Yoshihiko - Abstract:
- <abstract abstract-type="main" id="cas12286-abs-0001"> <title> <x xml:space="preserve">Abstract</x> </title> <p>The expression of podoplanin is reportedly involved in collective cell invasion, which is independent from the epithelial–mesenchymal transition (EMT). We focused on the expression of podoplanin in esophageal squamous cell carcinomas (ESCC) and investigated the correlation of podoplanin and EMT‐related markers, and evaluated its prognostic significance. Five ESCC cell lines were subjected to western blot analysis for podoplanin and EMT markers. The effects of podoplanin on EMT and carcinoma invasion were evaluated with wound healing assays, invasion assays and 3‐D culture. Transfection of ectopic podoplanin into a podoplanin‐negative ESCC cell line (TE‐15) induced cell migration and invasive activity (<italic>P</italic> &lt; 0.001 and <italic>P</italic> &lt; 0.05, respectively) without downregulation of E‐cadherin. In contrast, transfection of si‐podoplanin RNA into a podoplanin‐positive ESCC cell line (TE‐13) reduced cell migration and invasive activity (<italic>P</italic> &lt; 0.05). We reviewed 101 patients who had undergone esophagectomy for ESCC. Podoplanin expression was observed in 58 patients (57.4%), and positive expression was positively correlated with expression of E‐cadherin (<italic>P</italic> &lt; 0.01), deeper wall invasion (<italic>P</italic> &lt; 0.01), venous invasion (<italic>P</italic> &lt; 0.05) and poorer prognosis<abstract abstract-type="main" id="cas12286-abs-0001"> <title> <x xml:space="preserve">Abstract</x> </title> <p>The expression of podoplanin is reportedly involved in collective cell invasion, which is independent from the epithelial–mesenchymal transition (EMT). We focused on the expression of podoplanin in esophageal squamous cell carcinomas (ESCC) and investigated the correlation of podoplanin and EMT‐related markers, and evaluated its prognostic significance. Five ESCC cell lines were subjected to western blot analysis for podoplanin and EMT markers. The effects of podoplanin on EMT and carcinoma invasion were evaluated with wound healing assays, invasion assays and 3‐D culture. Transfection of ectopic podoplanin into a podoplanin‐negative ESCC cell line (TE‐15) induced cell migration and invasive activity (<italic>P</italic> &lt; 0.001 and <italic>P</italic> &lt; 0.05, respectively) without downregulation of E‐cadherin. In contrast, transfection of si‐podoplanin RNA into a podoplanin‐positive ESCC cell line (TE‐13) reduced cell migration and invasive activity (<italic>P</italic> &lt; 0.05). We reviewed 101 patients who had undergone esophagectomy for ESCC. Podoplanin expression was observed in 58 patients (57.4%), and positive expression was positively correlated with expression of E‐cadherin (<italic>P</italic> &lt; 0.01), deeper wall invasion (<italic>P</italic> &lt; 0.01), venous invasion (<italic>P</italic> &lt; 0.05) and poorer prognosis (<italic>P</italic> &lt; 0.01). Multivariate Cox analysis revealed that expression of podoplanin was a significant and independent unfavorable predictor of survival (<italic>P</italic> &lt; 0.05). These data suggest that podoplanin is significantly associated with and likely contributes to ESCC invasion in the absence of EMT.</p> </abstract> … (more)
- Is Part Of:
- Cancer science. Volume 104:Issue 12(2013:Dec.)
- Journal:
- Cancer science
- Issue:
- Volume 104:Issue 12(2013:Dec.)
- Issue Display:
- Volume 104, Issue 12 (2013)
- Year:
- 2013
- Volume:
- 104
- Issue:
- 12
- Issue Sort Value:
- 2013-0104-0012-0000
- Page Start:
- 1718
- Page End:
- 1725
- Publication Date:
- 2013-10-22
- Subjects:
- 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.12286 ↗
- 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
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 4135.xml