Grant Details
Grant Number: |
5R01CA067151-04 Interpret this number |
Primary Investigator: |
Li, Frederick |
Organization: |
Dana-Farber Cancer Institute |
Project Title: |
Inherited Msh2/Mlh1 Mutations in Colon Cancer Subgroups |
Fiscal Year: |
1998 |
Abstract
In recent months, 2 genes were identified for the common form of
hereditary colorectal cancer (hereditary non-polyposis colon cancer;
HNPCC). Based on small numbers of highly selected families, as much as 90%
of HNPCC might be attributable to these genes and carriers have an
estimated 70-90% lifetime risk of colorectal cancer. However, HNPCC
accounts for 4% or less of all colorectal cancers. The frequency of
inherited MSH2 and MLH1 mutations is unknown among the other 96% of all
colorectal cancers. Therefore, the aims of this population-based
epidemiological study are to determine the frequencies of germline MSH2
and MLH1 mutations (carriers) in a population-based, stratified sample of
400 colorectal cancer patients randomly selected from the Cancer
Surveillance Program of Orange, Imperial and San Diego Counties,
California. Study subjects will be sampled from strata defined by family
history of colorectal cancer (hereditary non-polyposis colon cancer,
familial cases but not HNPCC, and sporadic cases), and age at cancer
diagnosis (0-64 years, and 65 years and over). The results of mutational
status (its presence or absence, and mutation site and type within the
MSH2/MSH1 genes) will be correlated with data collated on family history,
age at diagnosis, and RER status, as well as clinical, demographic and
risk factor data from the questionnaire interview. The data from this
population-based study will facilitate strategic planning for translation
cancer control research that targets family members of subsets of
colorectal cancer cases.
Publications
Risk and risk reduction involving arginine intake and meat consumption in colorectal tumorigenesis and survival.
Authors: Zell J.A.
, Ignatenko N.A.
, Yerushalmi H.F.
, Ziogas A.
, Besselsen D.G.
, Gerner E.W.
, Anton-Culver H.
.
Source: International journal of cancer, 2007-02-01; 120(3), p. 459-68.
PMID: 17096347
Related Citations
Differential effects of wine consumption on colorectal cancer outcomes based on family history of the disease.
Authors: Zell J.A.
, McEligot A.J.
, Ziogas A.
, Holcombe R.F.
, Anton-Culver H.
.
Source: Nutrition and cancer, 2007; 59(1), p. 36-45.
PMID: 17927500
Related Citations
Characterization of hereditary nonpolyposis colorectal cancer families from a population-based series of cases.
Authors: Peel D.J.
, Ziogas A.
, Fox E.A.
, Gildea M.
, Laham B.
, Clements E.
, Kolodner R.D.
, Anton-Culver H.
.
Source: Journal of the National Cancer Institute, 2000-09-20; 92(18), p. 1517-22.
PMID: 10995807
Related Citations
Germ-line msh6 mutations in colorectal cancer families.
Authors: Kolodner R.D.
, Tytell J.D.
, Schmeits J.L.
, Kane M.F.
, Gupta R.D.
, Weger J.
, Wahlberg S.
, Fox E.A.
, Peel D.
, Ziogas A.
, et al.
.
Source: Cancer research, 1999-10-15; 59(20), p. 5068-74.
PMID: 10537275
Related Citations
Methylation of the hMLH1 promoter correlates with lack of expression of hMLH1 in sporadic colon tumors and mismatch repair-defective human tumor cell lines.
Authors: Kane M.F.
, Loda M.
, Gaida G.M.
, Lipman J.
, Mishra R.
, Goldman H.
, Jessup J.M.
, Kolodner R.
.
Source: Cancer research, 1997-03-01; 57(5), p. 808-11.
PMID: 9041175
Related Citations
Biochemistry and genetics of eukaryotic mismatch repair.
Authors: Kolodner R.
.
Source: Genes & development, 1996-06-15; 10(12), p. 1433-42.
PMID: 8666228
Related Citations
Mismatch repair: mechanisms and relationship to cancer susceptibility.
Authors: Kolodner R.D.
.
Source: Trends in biochemical sciences, 1995 Oct; 20(10), p. 397-401.
PMID: 8533151
Related Citations