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[Relationship between the expression of fragile histidine (FHIT) and the development of vulvar carcinoma].

AbstractOBJECTIVE:
To explore the relationship between the reduction of FHIT expression of fragile histidine (FHIT) and the development of vulvar carcinoma.
METHODS:
The expression of the FHIT product was detected by immunochemistry in the tissue samples of 20 normal vulvas, 22 vulvar intraepithelial neoplasias (VINs), and 60 primary vulvar carcinomas.
RESULTS:
The expressive rates of FHIT protein in the squamous epithelium of normal vulvas, VIN I - II, VIN II, and noninvasive and invasive vulvar carcinoma were 100% (20/20), 72.7% (8/11), 45.5% (5/11), and 21.7% (13/60) respectively (P<0.05). The expressive rates of FHIT protein in the well differentiated, intermediately differentiated and poorly differentiated invasive vulav carcinoma were 60.0% (9/15), 20.0% (3/15), and 3.3% (1/30) respectively (P<0.05). The expressive rate of the impaired FHIT protein in the invasive vulva carcinoma with lymphnode metastasis (10%) was lower than that without lymphnode metastasis (27.5%).
CONCLUSION:
Abnormal FHIT expression may play an important role in the progression of vulvar carcinoma. The expression of FHIT may provide important information for the prognosis of vulva carcinoma.
AuthorsYan-Xia Chu, Ai Zheng, Ming-Rong Xi, Jian Zhang
JournalSichuan da xue xue bao. Yi xue ban = Journal of Sichuan University. Medical science edition (Sichuan Da Xue Xue Bao Yi Xue Ban) Vol. 37 Issue 2 Pg. 218-20 (Mar 2006) ISSN: 1672-173X [Print] China
PMID16608079 (Publication Type: English Abstract, Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Neoplasm Proteins
  • fragile histidine triad protein
  • Acid Anhydride Hydrolases
Topics
  • Acid Anhydride Hydrolases (biosynthesis, genetics)
  • Adult
  • Aged
  • Aged, 80 and over
  • Carcinoma in Situ (metabolism)
  • Carcinoma, Squamous Cell (metabolism, pathology)
  • Female
  • Humans
  • Middle Aged
  • Neoplasm Proteins (biosynthesis, genetics)
  • Vulvar Neoplasms (metabolism, pathology)

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