## BACKGROUND. The progression of solid tumors is at least partly dependent on angiogenesis, the induction of which is mediated by several angiogenic factors, including angiogenin (ANG). The authors evaluated the expression of ANG in the tumor tissue and serum of patients with urothelial carcinoma
The expression of Fhit protein is related inversely to disease progression in patients with breast carcinoma
β Scribed by Zoran Gatalica; Subodh M. Lele; B. Alan Rampy; Brent A. Norris
- Publisher
- John Wiley and Sons
- Year
- 2000
- Tongue
- English
- Weight
- 549 KB
- Volume
- 88
- Category
- Article
- ISSN
- 0008-543X
No coin nor oath required. For personal study only.
β¦ Synopsis
BACKGROUND.
The FHIT gene, located at human chromosome 3p14.2, frequently is deleted in a number of human tumors, including breast carcinoma. Its protein product (Fhit) is presumed to have tumor suppressor function. Loss of expression of a tumor suppressor gene is an important step in tumor progression from premalignant, to in situ, to invasive carcinoma.
METHODS.
In the current study, Fhit expression was examined in invasive carcinomas and in epithelial lesions representing stages of carcinoma progression in 50 mastectomy specimens using immunohistochemical methods.
RESULTS.
Normal ductal and lobular epithelium consistently and strongly expressed Fhit. A complete loss of or a significant reduction in Fhit expression was observed in 72% of breast carcinomas. A statistically significant, negative correlation in Fhit expression among the stages of disease progression in Fhit negative breast carcinomas was observed (normal epithelium ΟΎ hyperplasia ΟΎ atypical hyperplasia and carcinoma in situ ΟΎ invasive carcinoma), whereas no loss of Fhit expression in precursor lesions was observed in Fhit positive tumors.
CONCLUSIONS.
These observations are consistent with the observed role of FHIT as a tumor suppressor gene in the pathogenesis of specific subsets of carcinomas.
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