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http://purl.uniprot.org/citations/21521534http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
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Background

The aim of this study was to clarify the clinical significance of TM4SF members CD9, CD63 and CD82 in human gastric carcinoma.

Methods

By employing RT-PCR and immunohistochemistry, we studied the expression of CD9, CD63 and CD82 in 49 paired tissue specimens of normal gastric mucosa and carcinoma. All tissues were obtained from patients who underwent curative surgery.

Results

All normal gastric epithelium and gastric ulcer tissues strongly expressed transcripts and proteins of CD9, CD63 and CD82 as compared with corresponding controls. We found a significant correlation between CD63 mRNA level and different pM statuses (P = 0.036). Carcinomas in M0 stage revealed a stronger expression of CD63 than carcinomas in M1 stage. Expression of CD9 protein was found significantly stronger in pN0, pM0 than in advanced pN stages (P = 0.03), pM1 (P = 0.013), respectively. We found the relationship between CD63 expression, gender (p = 0.09) and nodal status (p = 0.028), respectively. Additionally, advanced and metastasized tumor tissues revealed significantly down-regulated CD82 protein expression (p = 0.033 and p = 0, respectively), which correlated with the tumor pTNM stage (p = 0.001).

Conclusion

The reduction of CD9, CD63 and CD82 expression are indicators for the metastatic potential of gastric carcinoma cells. Unlike their expression in other tumor types, the constitutive expression of CD63 may indicate that this factor does play a direct role in human gastric carcinogenesis."xsd:string
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http://purl.uniprot.org/citations/21521534http://purl.uniprot.org/core/author"Chen Z."xsd:string
http://purl.uniprot.org/citations/21521534http://purl.uniprot.org/core/author"Gu S."xsd:string
http://purl.uniprot.org/citations/21521534http://purl.uniprot.org/core/author"Liu N."xsd:string
http://purl.uniprot.org/citations/21521534http://purl.uniprot.org/core/author"Zhu G."xsd:string
http://purl.uniprot.org/citations/21521534http://purl.uniprot.org/core/author"Hoang-Vu C."xsd:string
http://purl.uniprot.org/citations/21521534http://purl.uniprot.org/core/author"Dralle H."xsd:string
http://purl.uniprot.org/citations/21521534http://purl.uniprot.org/core/author"Trojanowicz B."xsd:string
http://purl.uniprot.org/citations/21521534http://purl.uniprot.org/core/date"2011"xsd:gYear
http://purl.uniprot.org/citations/21521534http://purl.uniprot.org/core/name"World J Surg Oncol"xsd:string
http://purl.uniprot.org/citations/21521534http://purl.uniprot.org/core/pages"43"xsd:string
http://purl.uniprot.org/citations/21521534http://purl.uniprot.org/core/title"Down-regulation of TM4SF is associated with the metastatic potential of gastric carcinoma TM4SF members in gastric carcinoma."xsd:string
http://purl.uniprot.org/citations/21521534http://purl.uniprot.org/core/volume"9"xsd:string
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