TY - JOUR
T1 - Association of HNPCC and endometrial cancers
AU - Banno, Kouji
AU - Susumu, Nobuyuld
AU - Yanokura, Megumi
AU - Hirao, Takeshi
AU - Iwata, Takashi
AU - Hirasawa, Akira
AU - Aoki, Daisuke
AU - Sugano, Kokichi
AU - Nozawa, Shiro
PY - 2004/8/1
Y1 - 2004/8/1
N2 - Hereditary nonpolyposis colorectal cancer (HNPCC) is among the representative familial cancers that are autosomally dominant inherited disorders. Because endometrial cancers develop at high rates in women with HNPCC, it is suggested that some endometrial cancers are familial cancers that are induced by mutations of the DNA mismatch repair (MMR) genes, as in HNPCC. To understand the clinical pathology of familial endometrial cancers that are associated with HNPCC, we surveyed the family histories of 385 patients with endometrial cancer and found that 0.5% of endometrial cancers met the new diagnostic criteria of HNPCC. From molecular and biological analyses, we found microsatellite instability in 30.8% of endometrial cancers and germline mutations of MMR genes in 8.3%. These results suggest a close relationship of MMR gene mutations to the development of endometrial cancers. For a better understanding of the clinical pathology of HNPCC-associated familial endometrial cancers, it is critical for gynecologists to perform a large multicenter study, including detailed family histories.
AB - Hereditary nonpolyposis colorectal cancer (HNPCC) is among the representative familial cancers that are autosomally dominant inherited disorders. Because endometrial cancers develop at high rates in women with HNPCC, it is suggested that some endometrial cancers are familial cancers that are induced by mutations of the DNA mismatch repair (MMR) genes, as in HNPCC. To understand the clinical pathology of familial endometrial cancers that are associated with HNPCC, we surveyed the family histories of 385 patients with endometrial cancer and found that 0.5% of endometrial cancers met the new diagnostic criteria of HNPCC. From molecular and biological analyses, we found microsatellite instability in 30.8% of endometrial cancers and germline mutations of MMR genes in 8.3%. These results suggest a close relationship of MMR gene mutations to the development of endometrial cancers. For a better understanding of the clinical pathology of HNPCC-associated familial endometrial cancers, it is critical for gynecologists to perform a large multicenter study, including detailed family histories.
KW - Endometrial cancer
KW - HNPCC
KW - Revised Amsterdam Criteria
KW - hMLH1
KW - hMSH2
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UR - http://www.scopus.com/inward/citedby.url?scp=4644262947&partnerID=8YFLogxK
U2 - 10.1007/s10147-004-0402-8
DO - 10.1007/s10147-004-0402-8
M3 - Review article
C2 - 15375702
AN - SCOPUS:4644262947
SN - 1341-9625
VL - 9
SP - 262
EP - 269
JO - International Journal of Clinical Oncology
JF - International Journal of Clinical Oncology
IS - 4
ER -