1996
DOI: 10.1002/(sici)1097-0142(19960515)77:10<2092::aid-cncr19>3.0.co;2-q
|View full text |Cite
|
Sign up to set email alerts
|

Expression of cell regulatory proteins in ovarian borderline tumors

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1
1

Citation Types

0
13
0

Year Published

1998
1998
2012
2012

Publication Types

Select...
10

Relationship

0
10

Authors

Journals

citations
Cited by 26 publications
(13 citation statements)
references
References 32 publications
0
13
0
Order By: Relevance
“…p16 and p53, as regulator genes of cell proliferation and apoptosis, are main targets in the chromosomal changes. p53 gene inactivation is the most common defect in ovarian cancer with a 60% mutation rate in advanced stage ovarian carcinoma whereas immunohistochemical p53 expression in SBTs varies from 0 to 33,3% (11)(12)(13)(14)(15)(16)(17)(18)(19)(20)(21). Ratio of p53 expression in SBTs is reported to be between benign and malignant tumors (15,(22)(23)(24).…”
Section: Discussionmentioning
confidence: 99%
“…p16 and p53, as regulator genes of cell proliferation and apoptosis, are main targets in the chromosomal changes. p53 gene inactivation is the most common defect in ovarian cancer with a 60% mutation rate in advanced stage ovarian carcinoma whereas immunohistochemical p53 expression in SBTs varies from 0 to 33,3% (11)(12)(13)(14)(15)(16)(17)(18)(19)(20)(21). Ratio of p53 expression in SBTs is reported to be between benign and malignant tumors (15,(22)(23)(24).…”
Section: Discussionmentioning
confidence: 99%
“…Most of the markers included in this category have been identified through approaches in which human cancer cells are used as an antigenic stimulus in animals to raise antibodies, which can then efficiently detect the antigen in human serum. A review of Table 1 suggests that CA 125 remains the best-documented and bestperforming single marker among the epithelial sialomucins currently described [2,6,47,48,54,63,91,94,98,101,102,108,112,116]. Sensitivity estimates vary from as low as 27% in some studies for early-staged disease to better than 90% for late-staged disease.…”
Section: Epithelial Sialomucinsmentioning
confidence: 99%
“…The most extensively studied oncogenes in ovarian tumors are HER‐2/neu oncogene and K‐ras oncogene. Overexpression of the HER‐2/neu oncogene occurs in approximately 30% of EOC and correlates with poor survival, whereas in BTO 21% overexpression is found without a clinical correlation (41–43) . There is no clear correlation between FIGO stage and HER‐2/neu gene expression.…”
Section: Etiologymentioning
confidence: 99%