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ShareMay 7, 2010 — Gastric cancer is the most common malignant gastrointestinal cancer and accounts for 25% of cancer deaths. Nuclear matrix, a filamentous protein framework for eukaryotic cellular chromatin, closely relates to DNA duplication and transcription. Research on nuclear matrix proteins will provide insight into how tumors developed.
A research article to be published on May 7, 2010 in the World Journal of Gastroenterology addresses this question. The research team from Xiamen University, China, investigated the aberrant expression of nuclear matrix proteins in human gastric cancer cells before and after hexamethylene bisacetamide (HMBA) treatment.
In the proteomics analysis, 43 protein spots were significantly changed due to HMBA treatment. Fifteen proteins were identified in the HMBA-induced differentiation of gastric tumor cells. Eight proteins spots were down-regulated while seven were up-regulated. Among these proteins, prohibitin, nucleophosmin and hnRNP A2/B1 were significantly decreased in HMBA-treated human gastric cancer cells, and their locations in nuclear matrix were altered by HMBA. The results proved the alteration of specific nuclear matrix proteins during the differentiation of human gastric cancer cells. And the aberrant expressions of nuclear matrix proteins were of significance in revealing the regulatory mechanism of tumor cell proliferation and differentiation.
The differentially expressed nuclear matrix proteins might be intracellular target proteins of HMBA and the tumor markers for gastric cancer. Continued investigation on specific nuclear matrix proteins will contribute to better understanding the regulatory mechanisms of nuclear matrix proteins in gastric carcinogenesis and reversal.
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The above story is reprinted from materials provided by World Journal of Gastroenterology, via EurekAlert!, a service of AAAS.
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Journal Reference:
- Jing GJ, Xu DH, Shi SL, Li QF, Wang SY, Wu FY, Kong HY. Aberrant expression of nuclear matrix proteins during HMBA-induced differentiation of gastric cancer cells. World Journal of Gastroenterology, 2010; 16 (17): 2176 DOI: 10.3748/wjg.v16.i17.2176
Note: If no author is given, the source is cited instead.
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