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Title:
High-level β1-integrin expression in a subpopulation of highly tumorigenic oral cancer cells | Clinical Oral Investigations
Description:
Objectives The β1 integrin (CD29) is a putative marker for cancerous epithelial stem cells. Cancer stem cells are essential to drive tumor growth, recurrence, and metastasis. We investigated the role of β1-integrin expression in the development of malignant phenotypes of oral squamous cell carcinoma (OSCC). Materials and methods Immunostaining was used to analyze the expression levels of β1 integrins in different types of cell colonies and tumor spheres. The results of cell viability and migration assays with and without siRNA knockdown of β1-integrin expression were compared. Cells expressing β1 integrins were evaluated for their tumorigenicity in mice. The expression of β1 integrins in human specimens of oral cancers at different clinical stages was semiquantified based on immunohistochemical staining of the β1-integrin protein. Results The expression level of β1 integrins in Meng-1 oral epidermoid carcinoma cells (OECM-1) cells was significantly higher in holoclonal colonies and tumor spheres compared to control cells. The knockdown of β1-integrin expression in OECM-1 cells reduced cell proliferation, migration, and tumor sphere formation. Beta-1 integrin (+) cells were more tumorigenic in the mouse xenograft model than β1 integrin (−) cells. In the human specimens, the expression level of the β1-integrin protein positively correlated with the clinical stage. Conclusion The expression of β1 integrin in OECM-1 cells is involved in the development of malignant phenotypes of OSCC. Clinical relevance Inhibitors for β1-integrin signaling may be suitable to become target-specific therapies for OSCC.
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article, pubmed, cancer, oral, google, scholar, cell, cells, integrin, expression, stem, carcinoma, squamous, human, βintegrin, integrins, res, tumor, signaling, central, clinical, access, head, neck, clin, privacy, cookies, content, chen, yuan, growth, beta, national, taiwan, university, publish, search, lin, huang, wong, kuo, model, oncol, metastatic, springer, cheng, kung, author, analysis, data,
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tung-yiu wong & kuo yuan high-level β1-integrin expression chao-liang wu integrin β1/fak/akt signaling month download article/chapter potential therapeutic target carcinoma-derived cell lines metastasis-related gene expression beta1 integrin-dependent activation squamous cell carcinoma neck cancer cells cancer stem cell cancer stem cells cancer stem cells lymph node metastasis full article pdf oral verrucous carcinoma β1-integrin protein related subjects tumor dormancy induced stem cell patterning target-specific therapies β1-integrin expression β1-integrin signaling ovarian cancer cells privacy choices/manage cookies suppresses metastatic ability engineering integrin signaling oral epithelial progenitors mouse xenograft model jehn-shyun huang alpha1beta1 integrin inhibitor article lin mouse skin carcinogenesis experimental melanoma growth national science council author information authors endothelial cell migration kuo yuan de moraes rv de fougerolles ar drive tumor growth epithelial-mesenchymal transition altered expression linked de luca lm allosteric signaling machines yuh-ling chen cancer stem check access instant access
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headline:High-level β1-integrin expression in a subpopulation of highly tumorigenic oral cancer cells
description:The β1 integrin (CD29) is a putative marker for cancerous epithelial stem cells. Cancer stem cells are essential to drive tumor growth, recurrence, and metastasis. We investigated the role of β1-integrin expression in the development of malignant phenotypes of oral squamous cell carcinoma (OSCC). Immunostaining was used to analyze the expression levels of β1 integrins in different types of cell colonies and tumor spheres. The results of cell viability and migration assays with and without siRNA knockdown of β1-integrin expression were compared. Cells expressing β1 integrins were evaluated for their tumorigenicity in mice. The expression of β1 integrins in human specimens of oral cancers at different clinical stages was semiquantified based on immunohistochemical staining of the β1-integrin protein. The expression level of β1 integrins in Meng-1 oral epidermoid carcinoma cells (OECM-1) cells was significantly higher in holoclonal colonies and tumor spheres compared to control cells. The knockdown of β1-integrin expression in OECM-1 cells reduced cell proliferation, migration, and tumor sphere formation. Beta-1 integrin (+) cells were more tumorigenic in the mouse xenograft model than β1 integrin (−) cells. In the human specimens, the expression level of the β1-integrin protein positively correlated with the clinical stage. The expression of β1 integrin in OECM-1 cells is involved in the development of malignant phenotypes of OSCC. Inhibitors for β1-integrin signaling may be suitable to become target-specific therapies for OSCC.
datePublished:2013-08-25T00:00:00Z
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Integrin
Oral cancer
Tumorigenesis
Stem cells
Dentistry
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headline:High-level β1-integrin expression in a subpopulation of highly tumorigenic oral cancer cells
description:The β1 integrin (CD29) is a putative marker for cancerous epithelial stem cells. Cancer stem cells are essential to drive tumor growth, recurrence, and metastasis. We investigated the role of β1-integrin expression in the development of malignant phenotypes of oral squamous cell carcinoma (OSCC). Immunostaining was used to analyze the expression levels of β1 integrins in different types of cell colonies and tumor spheres. The results of cell viability and migration assays with and without siRNA knockdown of β1-integrin expression were compared. Cells expressing β1 integrins were evaluated for their tumorigenicity in mice. The expression of β1 integrins in human specimens of oral cancers at different clinical stages was semiquantified based on immunohistochemical staining of the β1-integrin protein. The expression level of β1 integrins in Meng-1 oral epidermoid carcinoma cells (OECM-1) cells was significantly higher in holoclonal colonies and tumor spheres compared to control cells. The knockdown of β1-integrin expression in OECM-1 cells reduced cell proliferation, migration, and tumor sphere formation. Beta-1 integrin (+) cells were more tumorigenic in the mouse xenograft model than β1 integrin (−) cells. In the human specimens, the expression level of the β1-integrin protein positively correlated with the clinical stage. The expression of β1 integrin in OECM-1 cells is involved in the development of malignant phenotypes of OSCC. Inhibitors for β1-integrin signaling may be suitable to become target-specific therapies for OSCC.
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Oral cancer
Tumorigenesis
Stem cells
Dentistry
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Analytics and Tracking {📊}
- Google Tag Manager
Libraries {📚}
- Clipboard.js
- Prism.js
CDN Services {📦}
- Crossref