CommentaryHuman ovarian cancer of the surface epithelium
References (32)
- et al.
Epidermal growth factor receptor expression in normal ovarian epithelium and ovarian cancer. I. Correlation of receptor expression with prognostic factors in patients with ovarian cancer
Am J Obstet Gynecol
(1991) - et al.
Epidermal growth factor receptor expression in normal ovarian epithelium and ovarian cancer. II. Relationship between receptor expression and response to epidermal growth factor
Am J Obstet Gynecol
(1991) - et al.
Prognostic significance of HER-2/neu expression in advanced ovarian cancer
Am J Obstet Gynecol
(1993) - et al.
Neu protein overexpression in benign, borderline, and malignant ovarian neoplasms
Gynecol Oncol
(1992) - et al.
Regulation of growth of normal ovarian epithelial cells and ovarian cancer cell lines by transforming growth factor-β
Am J Obstet Gynecol
(1992) - et al.
Transforming growth factor-beta and ovarian carcinoma cells: Regulation of proliferation and surface antigen expression
Cancer Lett
(1990) - et al.
Growth regulation of ovarian cancer cells by epidermal growth factor and transforming growth factors α and β1
Biochim Biophys Acta
(1992) - et al.
Overexpression of p53 is not a feature of benign and early-stage borderline epithelial ovarian tumors
Gynecol Oncol
(1994) - et al.
Characteristics relating to ovarian cancer risk. Collaborative analysis of twelve US case-control studies. II. Invasive epithelial ovarian cancers in white women
Am J Epidemiol
(1992) Ovarian tumors of the hen
Environ Health Perspect
(1987)
The expression of EGF receptors, EGF-like factors and c-myc in ovarian and cervical carcinomas and their potential clinical significance
Anticancer Res
Studies of HER-2/neu proto-oncogene in human breast and ovarian cancer
Science
Overexpression of HER-2/neu is associated with poor survival in advanced epithelial ovarian cancer
Cancer Res
K-ras activation in neoplasms of the human female reproductive tract
Cancer Res
Somatic activation of rasK gene in a human ovarian carcinoma
Science
Evidence against ras activation in human ovarian carcinomas
Mol Biol Med
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Secretome proteomics for discovery of cancer biomarkers
2010, Journal of ProteomicsCitation Excerpt :Overall, this proteomic analysis revealed extensive shedding of extra cellular domains of cell surface proteins and high secretion rates in ovarian cancer cells [91]. Ascites fluid has attracted a lot of interest in the ovarian cancer biomarker research because it represents the local microenvironment secreted by ovarian tumors [92–95]. Gortzak-Uzan et al. [94] presented an in-depth proteomic analysis of human ovarian cancer ascites, resulting in the stringent and confident identification of over 2500 proteins by multidimensional protein identification technology (MudPIT) and gel enhanced LC-MS. In order to minimize these secreted proteins to a more manageable number of putative biomarkers for further investigation, the data were mapped against several recently published proteomic data sets of human plasma, urine, protein–protein interactions from the Interologous Interaction Database I2D (http://ophid.utoronto.ca/i2d) and 59 ovarian cancer related microarray data sets.
Biology and Pathology of Ovarian Cancer
2010, Early Diagnosis and Treatment of Cancer Series: Ovarian CancerMining the ovarian cancer ascites proteome for potential ovarian cancer biomarkers
2009, Molecular and Cellular ProteomicsA serum based analysis of ovarian epithelial tumorigenesis
2009, Gynecologic OncologyCitation Excerpt :The IPA software identified relationships between molecules in the two groups as shown in Fig. 2A. A similar analysis was performed for biomarkers we identified in our comparison of serous carcinomas with benign samples utilizing a list of genes including: AKT2[26,53], APOE2[27], BCL2[29], HLA-G[28], MK167[29], TP53[21–25], and WT1[9]. The results of this analysis are shown in Fig. 2B. Several of the genes examined are established players within molecular pathways widely considered to play a role in ovarian cancer.
Early detection and treatment of ovarian cancer: shifting from early stage to minimal volume of disease based on a new model of carcinogenesis
2008, American Journal of Obstetrics and GynecologyCitation Excerpt :In addition, type II tumors are characterized by considerable genetic instability, which is not observed in type I tumors. Most studies have shown that approximately 50-80% of advanced stage, presumably high-grade, serous carcinomas have mutant TP53.34-39 When purified tumor samples are analyzed, the frequency of TP53 mutations is over 80% in high-grade serous carcinomas.40
Gap junctions in the ovary: Expression, localization and function
2008, Molecular and Cellular Endocrinology