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遗传性非息肉病性结直肠癌中Ha-ras 1等位基因频率的分析。

Analysis of Ha-ras 1 allele frequencies in hereditary non-polyposis colorectal cancer.

作者信息

Jeevaratnam P, Browett P J, Van de Water N S, Jass J R

机构信息

Department of Molecular Medicine and Pathology, School of Medicine, University of Auckland, New Zealand.

出版信息

Gut. 1995 Mar;36(3):382-4. doi: 10.1136/gut.36.3.382.

DOI:10.1136/gut.36.3.382
PMID:7698697
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1382450/
Abstract

Restriction enzyme digests of genomic DNA show multiple alleles of common, intermediate, and rare frequencies at the minisatellite locus of Ha-ras. It has been suggested that a higher frequency of rare alleles is associated with the presence of colorectal and other types of cancer. This study investigated the distribution of Ha-ras alleles in 40 members of hereditary non-polyposis colorectal carcinoma (HNPCC) families and in 34 cancer free subjects (spouses). There was no difference in rare allele frequency between the cancer group and cancer free group (chi2 = 0.25, not significant).

摘要

基因组DNA的限制性酶切消化显示,在Ha-ras的小卫星位点存在常见、中等和罕见频率的多个等位基因。有人提出,罕见等位基因的较高频率与结直肠癌和其他类型癌症的存在有关。本研究调查了遗传性非息肉病性结直肠癌(HNPCC)家族的40名成员和34名无癌受试者(配偶)中Ha-ras等位基因的分布。癌症组和无癌组之间的罕见等位基因频率没有差异(χ2 = 0.25,无统计学意义)。

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本文引用的文献

1
Clues to the pathogenesis of familial colorectal cancer.家族性结直肠癌的发病机制线索。
Science. 1993 May 7;260(5109):812-6. doi: 10.1126/science.8484121.
2
Genetic mapping of a locus predisposing to human colorectal cancer.一个易患人类结直肠癌位点的基因定位。
Science. 1993 May 7;260(5109):810-2. doi: 10.1126/science.8484120.
3
Molecular biology of colorectal neoplasia.结直肠肿瘤的分子生物学
Gut. 1993 Mar;34(3):289-92. doi: 10.1136/gut.34.3.289.
4
An association between the risk of cancer and mutations in the HRAS1 minisatellite locus.癌症风险与HRAS1小卫星位点突变之间的关联。
N Engl J Med. 1993 Aug 19;329(8):517-23. doi: 10.1056/NEJM199308193290801.
5
Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancer.遗传性非息肉病性结直肠癌中一种MutS同源物的突变
Cell. 1993 Dec 17;75(6):1215-25. doi: 10.1016/0092-8674(93)90330-s.
6
The human mutator gene homolog MSH2 and its association with hereditary nonpolyposis colon cancer.人类错配修复基因同源物MSH2及其与遗传性非息肉病性结直肠癌的关联。
Cell. 1993 Dec 3;75(5):1027-38. doi: 10.1016/0092-8674(93)90546-3.
7
Genetic identification of Mom-1, a major modifier locus affecting Min-induced intestinal neoplasia in the mouse.Mom-1的基因鉴定,Mom-1是影响小鼠Min诱导的肠道肿瘤形成的一个主要修饰位点。
Cell. 1993 Nov 19;75(4):631-9. doi: 10.1016/0092-8674(93)90484-8.
8
Genetic mapping of a second locus predisposing to hereditary non-polyposis colon cancer.遗传性非息肉病性结直肠癌第二个易感位点的基因定位
Nat Genet. 1993 Nov;5(3):279-82. doi: 10.1038/ng1193-279.
9
Transforming genes in human tumors.人类肿瘤中的转化基因。
J Cell Biochem. 1982;20(1):51-61. doi: 10.1002/jcb.240200106.
10
Complete nucleotide sequences of the T24 human bladder carcinoma oncogene and its normal homologue.T24人膀胱癌癌基因及其正常同源基因的完整核苷酸序列。
Nature. 1983 Mar 3;302(5903):33-7. doi: 10.1038/302033a0.