Abstract | AIM: To detect the expression pattern of FAK ( focal adhesion kinase) and integrin alpha5 and beta1 subunits in different kinds of cancerous tissues and to study their correlation with clinicopathological data including tumor type, grade and lymph node status. METHODS: RESULTS: The staining of FAK was stronger in cancerous than in noncancerous areas. Enhanced expression of FAKwas detected in poor-differentiated carcinoma of the stomach and colorectum. Tumors with lymph node metastases had more FAK protein than those without metastases. In addition, the deeper the extent of tumor infiltration, the higher the FAK expression. The expression of integrin alpha5 and beta1 subunits was lower in cancerous areas than in noncancerous areas, but it was higher in well-differentiated cancerous tissues than in poor differentiated tissues. The relationship between the expression of integrin alpha5 and beta1 subunits and infiltration or metastasis was not significant. Cancerous tissues with stronger FAK expression (++ or +++) also had a higher expression of integrin alpha5 and beta1 subunits in the tumor and its unaffected margins. CONCLUSION:
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Authors | Jian-Min Su, Lu Gui, Yi-Ping Zhou, Xi-Liang Zha |
Journal | World journal of gastroenterology
(World J Gastroenterol)
Vol. 8
Issue 4
Pg. 613-8
(Aug 2002)
ISSN: 1007-9327 [Print] United States |
PMID | 12174366
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Antigens, CD
- Integrin alpha5
- Integrin beta1
- Protein-Tyrosine Kinases
- Focal Adhesion Kinase 1
- Focal Adhesion Protein-Tyrosine Kinases
- PTK2 protein, human
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Topics |
- Adult
- Aged
- Aged, 80 and over
- Antigens, CD
(metabolism)
- Breast Neoplasms
(metabolism, pathology)
- Colorectal Neoplasms
(metabolism, pathology)
- Female
- Focal Adhesion Kinase 1
- Focal Adhesion Protein-Tyrosine Kinases
- Humans
- Integrin alpha5
- Integrin beta1
(metabolism)
- Liver Neoplasms
(metabolism, pathology)
- Male
- Middle Aged
- Neoplasms
(metabolism, pathology)
- Protein-Tyrosine Kinases
(metabolism)
- Stomach Neoplasms
(metabolism, pathology)
- Uterine Neoplasms
(metabolism, pathology)
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