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International Journal of Cancer
Article . 2007 . Peer-reviewed
License: Wiley Online Library User Agreement
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Hereditary nonpolyposis colorectal cancer in endometrial cancer patients

Authors: Sang Nam, Yoon; Ja-Lok, Ku; Young-Kyoung, Shin; Kyung-Hee, Kim; Jin-Sung, Choi; Eun-Ja, Jang; Hyoung-Chul, Park; +11 Authors

Hereditary nonpolyposis colorectal cancer in endometrial cancer patients

Abstract

AbstractEndometrial cancer is the second most common cancer in hereditary nonpolyposis colorectal cancer (HNPCC). It has often been overlooked to explore the possibility of HNPCC in endometrial cancer patients. Our study was to investigate how many HNPCC patients existed among endometrial cancer patients. Among patients who underwent hysterectomy for endometrial cancer at Seoul National University Hospital from 1996 to 2004, 113 patients were included, whose family history and clinical data could be obtained and tumor specimens were available for microsatellite instability (MSI) testing and immunohistochemical (IHC) staining of MLH1, MSH2 and MSH6 proteins. There were 4 (3.5%) clinical HNPCC patients fulfilling the Amsterdam criteria II, and 2 (2/4, 50%) of them carried MSH2 germline mutations. There were also 8 (7.1%) suspected HNPCC (s‐HNPCC) patients fulfilling the revised criteria for s‐HNPCC, and one (1/8, 12.5%) of them revealed MLH1 germline mutation. In 101 patients, who were not clinical HNPCC or s‐HNPCC, 11 patients showed both MSI‐high and loss of expression of MLH1, MSH2 or MSH6 proteins, and 2 (2/11, 18.2%) of them showed MSH6 germline mutations. In 113 patients with endometrial cancer, we could find 5 (4.4%) HNPCC patients with MMR germline mutation and 2 (1.8%) clinical HNPCC patients without identified MMR gene mutation. Family history was critical in detecting 3 HNPCC patients with MMR germline mutation, and MSI testing with IHC staining for MLH1, MSH2 and MSH6 proteins was needed in the diagnosis of 2 HNPCC patients who were not clinical HNPCC or s‐HNPCC, especially for MSH6 germline mutation. © 2007 Wiley‐Liss, Inc.

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Keywords

Adult, DNA Mutational Analysis, Nuclear Proteins, Middle Aged, Colorectal Neoplasms, Hereditary Nonpolyposis, Immunohistochemistry, Polymerase Chain Reaction, Endometrial Neoplasms, DNA-Binding Proteins, Neoplasms, Multiple Primary, MutS Homolog 2 Protein, Tissue Array Analysis, Humans, Female, Microsatellite Instability, MutL Protein Homolog 1, Germ-Line Mutation, Adaptor Proteins, Signal Transducing, Aged

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    popularity
    This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
    Top 10%
    influence
    This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
    Top 10%
    impulse
    This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
    Top 10%
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selected citations
These citations are derived from selected sources.
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
26
Top 10%
Top 10%
Top 10%
bronze