Home LiteratureArticle Details
PMID: 7954427 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Loss of Apc+ in intestinal adenomas from Min mice.

Cancer research ·Vol. 54 ·No. 22 ·1994-11-15 ·Pages 5947-52

Luongo C, Moser AR, Gledhill S, Dove WF

Abstract

Allelic loss at the Apc locus in spontaneously occurring intestinal adenomas from mice heterozygous for the ApcMin nonsense mutation was analyzed using a site-specific quantitative polymerase chain reaction assay. All 97 of the intestinal adenomas analyzed showed extensive loss of the wild-type Apc (Apc+) allele. Quantitative polymerase chain reaction analysis of loci linked to Apc indicated loss of the chromosome carrying Apc+. Only one copy of the homologue carrying ApcMin remained in the intestinal adenomas. Possible reasons for the difference in the mechanism of Apc+ loss between human and Min mouse intestinal adenomas are discussed.

Related Genes
MeSH Terms
Adenoma/genetics Animals Base Sequence Chromosome Mapping Colonic Neoplasms/genetics DNA Probes/genetics Female Gene Deletion Genes, APC/genetics Intestinal Neoplasms/genetics Intestine, Small Male Mice Mice, Inbred AKR Molecular Sequence Data Polymerase Chain Reaction
Chemicals
DNA Probes
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Luongo C
McArdle Laboratory for Cancer Research, University of Wisconsin Medical School, Madison 53706.
Moser A R
Gledhill S
Dove W F
Article Info
Journal
Cancer research
Abbr.
Cancer Res
ISSN
0008-5472
Published
1994-11-15
Pages
5947-52
Language
English
Region
United States
NLM ID
2984705R
Subset
IM
Grants
PHS HHS · P01-23076 · United States
PHS HHS · R01-63677 · United States
NCI NIH HHS · R01-CA50585 · United States
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: [email protected]