These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Search MEDLINE/PubMed

  • Title: [Detection of chromosome 8 anomalies in ovarian carcinoma by fluorescence in situ hybridization].
    Author: Dong YL, Li CH, Chen LX, Feng HY, Zhu BS.
    Journal: Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2003 Feb; 20(1):59-60. PubMed ID: 12579504.
    Abstract:
    OBJECTIVE: To detect the relationship between chromosomal anomalies and the pathogenesis, development and prognosis of ovarian carcinoma. METHODS: Thirty-six specimens of ovarian carcinoma (n=12), ovarian benign tumor (n=12), and normal ovary (n=12) were examined by fluorescence in situ hybridization (FISH). RESULTS: Twelve cases of mutations, including trisomy 8, monosomy 8 or tetraploid 8 chromosomal anomalies, were found in the group of ovarian carcinoma, making up 100% (12/12). Three cases of trisomy 8 chromosomal anomalies were found in the group of ovarian benign tumor, accounting for 25% (3/12). No anomaly was found in the normal group. There were significant differences between the three groups, P<0.001. CONCLUSION: The above anomalies of chromosome 8 are significantly associated with the pathogenesis and development of ovarian carcinoma. The anomalies may occur in the early stage of the carcinoma, and may be significantly associated with the pathological differentiation and clinical stage of the case.
    [Abstract] [Full Text] [Related] [New Search]