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FHIT oncosuppressor gene expression profile in human anal cancers
C Zucchini1, M Concu, F Martini
1Molecular Genetics Research Center Fondazione CARISBO, Department of Histology, Embryology and Applied Biology, University of Bologna, Bologna, Italy.
Abstract:
The FHIT gene, a member of the histidine triad gene family, is a tumor suppressor gene exhibiting deletions in the majority of human cancers. Aberrant transcripts of this gene have been found in about 50% of esophageal, stomach and colon carcinomas. Little is known about the molecular mechanisms involved in malignant transformation of the lining cells of the anus. In this study FHIT gene expression was investigated in this particular kind of human cancer. FHIT expression was comparatively analyzed at the mRNA level, by RT-PCR, in squamous anal cancers, normal anal tissue and peripheral blood samples. cDNA analyses showed variability in FHIT transcripts, without apparent effects on the predicted amino acid sequence. These different FHIT mRNAs could represent transcripts from an alternative splicing event. Our data indicate that the FHIT mRNA detected in anal cancers and in normal samples is heterogeneous. Immunohistochemical data suggest that the Fhit protein is expressed only in a fraction of the tumor cells, while it is strongly expressed in the epithelial cells of glands of the normal anal mucosa. The absence or poor expression of the Fhit protein in anal cancers suggests a role for this tumor suppressor gene product, as a risk factor, in the onset of this human cancer, as reported before for other human gastrointestinal tumors.
Insights
The FHIT gene, a tumor suppressor, shows reduced expression in anal cancers. Its absence or low levels in tumors suggest it may be a risk factor for this cancer.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- The FHIT gene, part of the histidine triad gene family, is a known tumor suppressor.
- Deletions and aberrant transcripts of FHIT are observed in various human cancers, including gastrointestinal tumors.
- Molecular mechanisms of anal cancer development are not well understood.
Purpose of the Study:
- To investigate FHIT gene expression in squamous anal cancer.
- To compare FHIT mRNA and protein levels in cancerous and normal anal tissues.
Main Methods:
- Reverse transcription-polymerase chain reaction (RT-PCR) was used to analyze FHIT mRNA levels.
- Immunohistochemistry was employed to assess Fhit protein expression.
- Anal cancer tissues, normal anal tissue, and peripheral blood samples were analyzed.
Main Results:
- FHIT mRNA transcripts in anal cancers and normal tissues were heterogeneous, potentially due to alternative splicing.
- Fhit protein expression was significantly reduced or absent in anal cancer cells compared to normal anal glands.
- Normal anal mucosa showed strong Fhit protein expression in epithelial cells of glands.
Conclusions:
- Reduced or absent Fhit protein expression in anal cancer suggests its role as a tumor suppressor.
- FHIT may function as a risk factor in the development of anal cancer.
- The findings align with previous observations in other gastrointestinal tumors.
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