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Hereditary nonpolyposis colorectal cancer in endometrial cancer patients
Authors:Yoon Sang Nam  Ku Ja-Lok  Shin Young-Kyoung  Kim Kyung-Hee  Choi Jin-Sung  Jang Eun-Ja  Park Hyoung-Chul  Kim Duck-Woo  Kim Min A  Kim Woo Ho  Lee Taek Sang  Kim Jae Weon  Park Noh-Hyun  Song Yong-Sang  Kang Soon-Beom  Lee Hyo-Pyo  Jeong Seung-Yong  Park Jae-Gahb
Affiliation:Korean Hereditary Tumor Registry, Cancer Research Institute, Seoul National University, Seoul, Korea.
Abstract:Endometrial 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.
Keywords:endometrial cancer  hereditary nonpolyposis colorectal cancer (HNPCC)  microsatellite instability (MSI)  mismatch repair gene (MMR)  MLH1  MSH2  MSH6
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