Results 41 to 50 of about 7,566,127 (187)
The development and progression of colorectal cancer (CRC) is a multi-step process, and the Wnt pathways with its two molecular gladiators adenomatous polyposis coli (APC) and β-catenin plays an important role in transforming a normal tissue into a ...
Sameer A +4 more
doaj +1 more source
The tumor suppressor gene adenomatous polyposis coli (APC) is the initiating mutation in approximately 80% of all colorectal cancers (CRC), underscoring the importance of aberrant regulation of intracellular WNT signaling in CRC development.
Adam Grant +8 more
doaj +1 more source
Statin Treatment as a Targeted Therapy for APC-Mutated Colorectal Cancer
BackgroundMutations in the tumor suppressor gene Adenomatous Polyposis Coli (APC) are found in 80% of sporadic colorectal cancer (CRC) tumors and are also responsible for the inherited form of CRC, Familial adenomatous polyposis (FAP).MethodsTo identify ...
Hannah Shailes +4 more
doaj +1 more source
Differential RNA-seq analysis comparing APC-defective and APC-restored SW480 colorectal cancer cells
The adenomatous polyposis coli (APC) tumour suppressor gene is mutated in about 80% of colorectal cancers (CRC) Brannon et al. (2014) [1]. APC is a large multifunctional protein that regulates many biological functions including Wnt signalling (through ...
Lauren E. King +4 more
doaj +1 more source
Expression Profiles in Stage II Colon Cancer According to APC Gene Status.
Colorectal cancer is one of the most common cancers in the world. Histoclinical staging is efficient, but combination with molecular markers may improve the classification of stage II cancers.
D. Birnbaum +7 more
semanticscholar +1 more source
Rare mutations predisposing to familial adenomatous polyposis in Greek FAP patients
Background Familial Adenomatous Polyposis (FAP) is caused by germline mutations in the APC (Adenomatous Polyposis Coli) gene. The vast majority of APC mutations are point mutations or small insertions / deletions which lead to truncated protein products.
Danielidis Ioannis +11 more
doaj +1 more source
APC and MUTYH Analysis in FAP Patients: A Novel Mutation in APC Gene and Genotype-Phenotype Correlation [PDF]
APC and MUTYH genes are mutated in 70–90% and 10–30% of familial adenomatous polyposis cases (FAP) respectively. An association between mutation localization and FAP clinical phenotype is reported. The aims of this study were to determine APC and MUTYH mutational status in a small cohort of FAP patients and to evaluate the genotype-phenotype ...
D'Elia G. +5 more
openaire +2 more sources
Mutational spectrum of
Background Familial adenomatous polyposis, an autosomal dominant inherited disease caused by germline mutations within the APC gene, is characterized by early onset colorectal cancer as a consequence of the intrinsic phenotypic feature of multiple ...
Fountzilas George +4 more
doaj +1 more source
Familial Adenomatous Polyposis: An Uncommon Autosomal Genetic Condition [PDF]
A 40-year-old man presented to the Department of Emergency Medicine with severe pain in abdomen which was present for the past two days. He experienced three episodes of vomiting and two episodes of diarrhoea which was greenish in colour without any ...
Simran Khan, Shreya Giri, Suhit Naseri
doaj +1 more source
BACKGROUND: Some of colorectal cancers (CRCs) are familial, however, heterozygote relatives have approximately 80% lifetime risk of cancer. Risk assessment of CRC’s family could be calculated by direct measurement of mRNA gene expression and Bayesian ...
Tjahjadi Robert Tedjasaputra +13 more
doaj +1 more source

