Decreased expression of kallikrein‐related peptidase 13: Possible contribution to metastasis of human oral cancer. Issue 7 (31st January 2013)
- Record Type:
- Journal Article
- Title:
- Decreased expression of kallikrein‐related peptidase 13: Possible contribution to metastasis of human oral cancer. Issue 7 (31st January 2013)
- Main Title:
- Decreased expression of kallikrein‐related peptidase 13: Possible contribution to metastasis of human oral cancer
- Authors:
- Ishige, Shunsaku
Kasamatsu, Atsushi
Ogoshi, Kenji
Saito, Yasuhiro
Usukura, Katsuya
Yokoe, Hidetaka
Kouzu, Yukinao
Koike, Hirofumi
Sakamoto, Yosuke
Ogawara, Katsunori
Shiiba, Masashi
Tanzawa, Hideki
Uzawa, Katsuhiro - Abstract:
- <abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <sec id="mc22007-sec-0001" sec-type="section"> <p>The human kallikrein‐related peptidase family is comprised of 15 serine protease genes on chromosome 19q13.4 <xref ref-type="link" rid="mc22007-bib-0001">1</xref>. Our previous microarray analyses showed that the gene <italic>kallikrein‐related peptidase 13</italic> (<italic>KLK13</italic>) was down‐regulated in oral squamous cell carcinoma (OSCC) cell lines. We evaluated the expression status of KLK13 in primary OSCCs and performed functional molecular experiments in OSCC cell lines. In 102 primary tumors studied, KLK13 expression significantly (<italic>P</italic> &lt; 0.05) decreased compared with matched normal counterparts. Interestingly, KLK13‐negative cases correlated significantly (<italic>P</italic> &lt; 0.05) with regional lymph node metastasis. In vitro, cells overexpressing KLK13 (oeKLK13) had decreased invasiveness and motility and up‐regulation of adhesion molecules (E‐cadherin, α‐catenin, β‐catenin, junction plakoglobin, plakophilin4, desmocollin2, desmoglein3, and desmoplakin) compared with control cells. A rescue experiment that transfected oeKLK13 cells with siRNA against KLK13 restored invasiveness and migration activities with down‐regulated adhesion molecules. Based on our results, we concluded that KLK13 may play an important role in regulating cellular migration and invasiveness, making the loss of KLK13 a potential biomarker for early<abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <sec id="mc22007-sec-0001" sec-type="section"> <p>The human kallikrein‐related peptidase family is comprised of 15 serine protease genes on chromosome 19q13.4 <xref ref-type="link" rid="mc22007-bib-0001">1</xref>. Our previous microarray analyses showed that the gene <italic>kallikrein‐related peptidase 13</italic> (<italic>KLK13</italic>) was down‐regulated in oral squamous cell carcinoma (OSCC) cell lines. We evaluated the expression status of KLK13 in primary OSCCs and performed functional molecular experiments in OSCC cell lines. In 102 primary tumors studied, KLK13 expression significantly (<italic>P</italic> &lt; 0.05) decreased compared with matched normal counterparts. Interestingly, KLK13‐negative cases correlated significantly (<italic>P</italic> &lt; 0.05) with regional lymph node metastasis. In vitro, cells overexpressing KLK13 (oeKLK13) had decreased invasiveness and motility and up‐regulation of adhesion molecules (E‐cadherin, α‐catenin, β‐catenin, junction plakoglobin, plakophilin4, desmocollin2, desmoglein3, and desmoplakin) compared with control cells. A rescue experiment that transfected oeKLK13 cells with siRNA against KLK13 restored invasiveness and migration activities with down‐regulated adhesion molecules. Based on our results, we concluded that KLK13 may play an important role in regulating cellular migration and invasiveness, making the loss of KLK13 a potential biomarker for early detection of lymph node metastasis in OSCCs. © 2013 Wiley Periodicals, Inc.</p> </sec> </abstract> … (more)
- Is Part Of:
- Molecular carcinogenesis. Volume 53:Issue 7(2014:Jul.)
- Journal:
- Molecular carcinogenesis
- Issue:
- Volume 53:Issue 7(2014:Jul.)
- Issue Display:
- Volume 53, Issue 7 (2014)
- Year:
- 2014
- Volume:
- 53
- Issue:
- 7
- Issue Sort Value:
- 2014-0053-0007-0000
- Page Start:
- 557
- Page End:
- 565
- Publication Date:
- 2013-01-31
- Subjects:
- Carcinogenesis -- Molecular aspects -- Periodicals
616.994071 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1098-2744 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/mc.22007 ↗
- Languages:
- English
- ISSNs:
- 0899-1987
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5900.802000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 4054.xml