Inherited susceptibility to colorectal adenomas and carcinomas: Evidence for a new predisposition gene on 15q14-q22

被引:71
作者
Tomlinson, I
Rahman, N
Frayling, I
Mangion, J
Barfoot, R
Hamoudi, R
Seal, S
Northover, J
Thomas, HJW
Neale, K
Hodgson, S
Talbot, I
Houlston, R
Stratton, MR [1 ]
机构
[1] Inst Canc Res, Haddow Labs, Sect Canc Genet, Sutton SM2 5NG, Surrey, England
[2] Univ Oxford, Radcliffe Hosp, Dept Clin Med, Oxford, England
[3] Imperial Canc Res Fund, Mol & Populat Genet Lab, London WC2A 3PX, England
[4] St Marks & Northwick Pk NHS Trust, Imperial Canc Res Fund, Colorectal Canc Unit, Harrow, Middx, England
[5] St Marks Hosp, Polyposis Registry, Harrow, Middx, England
[6] Guys Hosp, Dept Clin Genet, London SE1 9RT, England
[7] St Marks Hosp, Dept Pathol, Harrow, Middx, England
基金
英国医学研究理事会;
关键词
D O I
10.1016/S0016-5085(99)70061-2
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background & Aims: The aim of this study was to evaluate the role of known colorectal adenoma and carcinoma susceptibility genes and to locate a novel susceptibility gene in an Ashkenazi family (SM1311) with dominantly inherited predisposition to colorectal adenomas and carcinomas. Methods: Clinicopathologic and family history data were collected. Genetic linkage and mutational analyses were used to investigate the genetic basis of the family's disease. Results: Affected members of SM1311 develop multiple tubular, villous, tubulovillous, and/or serrated colorectal adenomas throughout the large bowel, and some develop colon carcinoma. There are no extracolonic features clearly associated with disease in SM1311. We have shown that the family's phenotype does not result from APC mutations (including the l1307K variant) or from genetic changes in the other known genes that predispose to colon cancer. Using genetic linkage analysis, supplemented by allele loss in tumors, we have provided evidence for a new colorectal cancer susceptibility gene, CRAC1 (colorectal adenoma and carcinoma), mapping to chromosome 15q14-q22. Conclusions: We provide evidence for a novel colorectal adenoma and carcinoma susceptibility gene on chromosome 15q14-q22. Further studies are needed to confirm this localization and to evaluate the contribution of CRAC1. to this disease.
引用
收藏
页码:789 / 795
页数:7
相关论文
共 46 条
[1]   Life-time risk of different cancers in hereditary non-polyposis colorectal cancer (HNPCC) syndrome [J].
Aarnio, M ;
Mecklin, JP ;
Aaltonen, LA ;
NystromLahti, M ;
Jarvinen, HJ .
INTERNATIONAL JOURNAL OF CANCER, 1995, 64 (06) :430-433
[2]  
ALBRIGHT LAC, 1988, NEW ENGL J MED, V319, P533
[3]   Frequency of germline hereditary non-polyposis colorectal cancer gene mutations in patients with multiple or early onset colorectal adenomas [J].
Beck, NE ;
Tomlinson, IPM ;
Homfray, TFR ;
Frayling, IM ;
Hodgson, SV ;
Bodmer, WF .
GUT, 1997, 41 (02) :235-238
[4]   APC gene: Database of germline and somatic mutations in human tumors and cell lines [J].
Beroud, C ;
Soussi, T .
NUCLEIC ACIDS RESEARCH, 1996, 24 (01) :121-124
[5]  
BONELLI L, 1988, INT J CANCER, V41, P513
[6]  
BURT RW, 1990, B WORLD HEALTH ORGAN, V68, P655
[7]   Mutations of mitotic checkpoint genes in human cancers [J].
Cahill, DP ;
Lengauer, C ;
Yu, J ;
Riggins, GJ ;
Willson, JKV ;
Markowitz, SD ;
Kinzler, KW ;
Vogelstein, B .
NATURE, 1998, 392 (6673) :300-303
[8]  
DELEON MP, 1987, CANCER, V60, P2848, DOI 10.1002/1097-0142(19871201)60:11<2848::AID-CNCR2820601141>3.0.CO
[9]  
2-F
[10]   Localization of a susceptibility locus for Peutz-Jeghers syndrome to 19p using comparative genomic hybridization and targeted linkage analysis [J].
Hemminki, A ;
Tomlinson, I ;
Markie, D ;
Jarvinen, H ;
Sistonen, P ;
Bjorkqvist, AM ;
Knuutila, S ;
Salovaara, R ;
Bodmer, W ;
Shibata, D ;
delaChapelle, A ;
Aaltonen, LA .
NATURE GENETICS, 1997, 15 (01) :87-90