Literature DB >> 16226103

Nuclear size distinguishes low- from high-grade ovarian serous carcinoma and predicts outcome.

Chih-Yi Hsu1, Robert J Kurman, Russell Vang, Tian-Li Wang, Jan Baak, Ie-Ming Shih.   

Abstract

A dualistic model for ovarian serous carcinogenesis based on morphological and molecular genetic studies has recently been proposed. This model divides serous carcinoma into low- and high-grade tumors, which develop along distinct molecular pathways. In this report, we evaluated computerized morphometry to determine its utility in distinguishing low- and high-grade serous carcinoma. The mean nuclear area (MNA) and the volume percentage of epithelium (VPE) in 93 high-grade serous carcinomas was measured and compared with 16 low-grade serous carcinomas and 21 serous borderline tumors, the putative precursor of low-grade serous carcinoma. We found that both MNA and VPE were significantly higher in high-grade serous carcinoma compared with low-grade serous carcinoma and serous borderline tumors (P < .001 and P = .02, respectively). There was no significant difference in MNA and VPE between low-grade carcinoma and serous borderline tumors (P > .3). Among high-grade serous carcinomas, those with an MNA of 46 microm2 or higher had a poorer survival (P = .035) than those with an MNA below 46 microm2. In contrast, VPE and tumor grade (moderately versus poorly differentiated) had no significant prognostic value. The morphometry findings lend further support to the dualistic model of ovarian serous carcinogenesis and suggest that MNA is an excellent adjunctive tool for distinguishing low- from high-grade serous carcinomas. In addition, MNA is an independent prognostic factor for high-grade serous carcinoma.

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Year:  2005        PMID: 16226103     DOI: 10.1016/j.humpath.2005.07.014

Source DB:  PubMed          Journal:  Hum Pathol        ISSN: 0046-8177            Impact factor:   3.466


  13 in total

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Review 2.  Ovarian low-grade and high-grade serous carcinoma: pathogenesis, clinicopathologic and molecular biologic features, and diagnostic problems.

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4.  Dependence of temporal diffusion spectra on microstructural properties of biological tissues.

Authors:  Junzhong Xu; Mark D Does; John C Gore
Journal:  Magn Reson Imaging       Date:  2010-12-03       Impact factor: 2.546

5.  Quantitative characterization of tissue microstructure with temporal diffusion spectroscopy.

Authors:  Junzhong Xu; Mark D Does; John C Gore
Journal:  J Magn Reson       Date:  2009-07-03       Impact factor: 2.229

6.  Sensitivity of MR diffusion measurements to variations in intracellular structure: effects of nuclear size.

Authors:  Junzhong Xu; Mark D Does; John C Gore
Journal:  Magn Reson Med       Date:  2009-04       Impact factor: 4.668

7.  Defining the cut point between low-grade and high-grade ovarian serous carcinomas: a clinicopathologic and molecular genetic analysis.

Authors:  Ayse Ayhan; Robert J Kurman; Anna Yemelyanova; Russell Vang; Sanjay Logani; Jeffrey D Seidman; Ie-Ming Shih
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8.  Integrated analysis of gene expression and tumor nuclear image profiles associated with chemotherapy response in serous ovarian carcinoma.

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9.  Nuclear envelope structural defects cause chromosomal numerical instability and aneuploidy in ovarian cancer.

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10.  Loss of A-type lamin expression compromises nuclear envelope integrity in breast cancer.

Authors:  Callinice D Capo-chichi; Kathy Q Cai; Jennifer Smedberg; Parvin Ganjei-Azar; Andrew K Godwin; Xiang-Xi Xu
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