RACIAL VARIATION IN THE DISTRIBUTION OF HA-RAS-1 ALLELES

被引:28
作者
WESTON, A
VINEIS, P
CAPORASO, NE
KRONTIRIS, TG
LONERGAN, JA
SUGIMURA, H
机构
[1] NCI,ENVIRONM EPIDEMIOL BRANCH,BETHESDA,MD 20892
[2] UNIV TURIN,CANC EPIDEMIOL UNIT,I-10124 TURIN,ITALY
[3] TUFTS UNIV,NEW ENGLAND MED CTR,DEPT MED HEMATOL ONCOL,BOSTON,MA 02111
关键词
RESTRICTION FRAGMENT LENGTH POLYMORPHISMS; VARIABLE TANDEM REPEATS; ONCOGENE; EPIDEMIOLOGY; CARCINOGENESIS;
D O I
10.1002/mc.2940040404
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Restriction fragment length polymorphism analyses of the Ha-ras-1 proto-oncogene were undertaken in white and black populations residing in the Baltimore-Washington metropolitan area to address whether specific rare alleles of the Ha-ras-1 proto-oncogene locus vary in their distribution among different racial groups. High-molecular-weight genomic DNA samples from the lungs of 80 lung cancer patients and 92 accident victims were digested with appropriate restriction enzymes and subjected to Southern analysis using the 6.6-kb BamHl human Ha-ras-1 recombinant fragment from the plasmid pEC. Thirty allelomorphs of different sizes were detected among the 172 study subjects. An association was observed between race and specific alleles. Rare alleles were more frequent in black cancer patients and trauma victims than in whites. Within each racial category, lung cancer patients had an excess of rare alleles. These data indicate the importance of controlling for racial variation when designing studies to determine human cancer risk factors.
引用
收藏
页码:265 / 268
页数:4
相关论文
共 29 条
[1]   REDUCTION TO HOMOZYGOSITY OF GENES ON CHROMOSOME-11 IN HUMAN-BREAST NEOPLASIA [J].
ALI, IU ;
LIDEREAU, R ;
THEILLET, C ;
CALLAHAN, R .
SCIENCE, 1987, 238 (4824) :185-188
[2]  
BAIRD M, 1986, AM J HUM GENET, V39, P489
[3]   COMPLETE NUCLEOTIDE-SEQUENCES OF THE T24 HUMAN BLADDER-CARCINOMA ONCOGENE AND ITS NORMAL HOMOLOG [J].
CAPON, DJ ;
CHEN, EY ;
LEVINSON, AD ;
SEEBURG, PH ;
GOEDDEL, DV .
NATURE, 1983, 302 (5903) :33-37
[4]   THE HA-RAS POLYMORPHISM IN MYELODYSPLASIA AND ACUTE MYELOID-LEUKEMIA [J].
CARTER, G ;
WORWOOD, M ;
JACOBS, A .
LEUKEMIA RESEARCH, 1988, 12 (05) :385-&
[5]   RARE HA-RAS AND C-MOS ALLELES IN PATIENTS WITH INTRACRANIAL TUMORS [J].
DIEDRICH, U ;
ECKERMANN, O ;
SCHMIDTKE, J .
NEUROLOGY, 1988, 38 (04) :587-589
[6]   HYPOMETHYLATION OF RAS ONCOGENES IN PRIMARY HUMAN CANCERS [J].
FEINBERG, AP ;
VOGELSTEIN, B .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1983, 111 (01) :47-54
[7]   EVIDENCE AGAINST HA-RAS-1 INVOLVEMENT IN SPORADIC AND FAMILIAL MELANOMA [J].
GERHARD, DS ;
DRACOPOLI, NC ;
BALE, SJ ;
HOUGHTON, AN ;
WATKINS, P ;
PAYNE, CE ;
GREENE, MH ;
HOUSMAN, DE .
NATURE, 1987, 325 (6099) :73-75
[8]   GENETIC PREDISPOSITION TO HUMAN-LUNG CANCER [J].
HEIGHWAY, J ;
THATCHER, N ;
CERNY, T ;
HASLETON, PS .
BRITISH JOURNAL OF CANCER, 1986, 53 (04) :453-457
[9]   LACK OF CORRELATION BETWEEN RARE HA-RAS ALLELES AND UROTHELIAL CANCER IN JAPAN [J].
ISHIKAWA, J ;
MAEDA, S ;
TAKAHASHI, R ;
KAMIDONO, S ;
SUGIYAMA, T .
INTERNATIONAL JOURNAL OF CANCER, 1987, 40 (04) :474-478
[10]   HUMAN RESTRICTION-FRAGMENT-LENGTH-POLYMORPHISMS AND CANCER RISK ASSESSMENT [J].
KRONTIRIS, TG ;
DIMARTINO, NA ;
COLB, M ;
MITCHESON, HD ;
PARKINSON, DR .
JOURNAL OF CELLULAR BIOCHEMISTRY, 1986, 30 (04) :319-329