» Articles » PMID: 7954427

Loss of Apc+ in Intestinal Adenomas from Min Mice

Overview
Journal Cancer Res
Specialty Oncology
Date 1994 Nov 15
PMID 7954427
Citations 136
Authors
Affiliations
Soon will be listed here.
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.

Citing Articles

Exploration of different quantitative polymerase chain reaction-based genotyping methods to distinguish Apcmin/+ mice from wildtype mice.

Sun Y, Zhou T, Ye S, Lau E, Zeng Y, Liang J PLoS One. 2025; 20(2):e0317038.

PMID: 39903728 PMC: 11793731. DOI: 10.1371/journal.pone.0317038.


Plasma-Derived Extracellular Vesicles and Non-Extracellular Vesicle Components from APC Mice Promote Pro-Tumorigenic Activities and Activate Human Colonic Fibroblasts via the NF-κB Signaling Pathway.

Arteaga-Blanco L, Evans A, Dixon D Cells. 2024; 13(14).

PMID: 39056778 PMC: 11274984. DOI: 10.3390/cells13141195.


Cancer-on-a-chip model shows that the adenomatous polyposis coli mutation impairs T cell engagement and killing of cancer spheroids.

Bonnet V, Maikranz E, Madec M, Vertti-Quintero N, Cuche C, Mastrogiovanni M Proc Natl Acad Sci U S A. 2024; 121(11):e2316500121.

PMID: 38442157 PMC: 10945811. DOI: 10.1073/pnas.2316500121.


Tumor-Promoting Role of GNA14 in Colon Cancer Development.

Park R, Lee S, Chin H, Nguyen A, Lee D Cancers (Basel). 2023; 15(18).

PMID: 37760541 PMC: 10527020. DOI: 10.3390/cancers15184572.


Interstitial deletion of the Apc locus in β-catenin-overexpressing cells is a signature of radiation-induced intestinal tumors in C3B6F1 ApcMin/+ mice†.

Yanagihara H, Morioka T, Yamazaki S, Yamada Y, Tachibana H, Daino K J Radiat Res. 2023; 64(3):622-631.

PMID: 37117033 PMC: 10215001. DOI: 10.1093/jrr/rrad021.