The G 1 /S checkpoint of the cell cycle is regulated by p16, p53 and RB tumor suppressor genes. Loss of expression of the p16 INK4 tumor suppressor protein, the product of the CDKN2 gene, has been associated with a wide variety of human malignancies. Mutations, loss of heterozygosity and deletions o
Melanoma antigen-encoding gene-1 expression in invasive gastric carcinoma: Correlation with stage of disease
β Scribed by Katano, Mitsuo; Nakamura, Mitsunari; Morisaki, Takashi; Fujimoto, Kazuma
- Publisher
- John Wiley and Sons
- Year
- 1997
- Tongue
- English
- Weight
- 156 KB
- Volume
- 64
- Category
- Article
- ISSN
- 0022-4790
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β¦ Synopsis
Background:
A human melanoma antigen-encoding gene-1, mage-1 gene, may be linked to the neoplastic transformation. in the present study, we extended this association with human gastric carcinomas. specifically, we focused on the relationship between mage-1 gene expression and the histologic stage of gastric carcinoma.
Methods:
We used a reverse transcription-polymerase chain reaction assay (rt-pcr) to analyze the expression of the mage-1 gene in 38 endoscopic biopsy specimens from gastric carcinomas. we also studied the relationship between the expression of mage-1 gene and the genetic expression of several tumor invasion-related factors, including 72 kd type iv collagenase (mmp2), urokinase-type plasminogen activator (upa), platelet-derived growth factor a (pdgf-a), and vascular endothelial growth factor (vegf).
Results:
Eleven of the 38 tumor samples (28.9%) expressed the mage-1 gene. mage-1 gene expression was present only in two of the 38 adjacent nontumor samples (5.3%). mage-1 gene expression in the 38 tumor samples was significantly correlated with the histological stage of disease (p = 0.0008), especially with the depth of histologically confirmed tumor invasion (t1 vs. t2 or greater, p = 0.00048). the expression of mage-1 gene correlated with the expression of mmp2 (p = 0.0064), upa (p = 0.0390), and pdgf-a (p = 0.00018).
Conclusions:
These data suggest that the mage-1 gene may be activated in gastric carcinomas during periods of their development or invasion. in addition, a relationship between mage-1 gene expression and expression of invasion-related factors has been demonstrated.
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