Hereditary Nonpolyposis Colorectal Cancer
|
0.700 |
GeneticVariation
|
disease |
BEFREE |
We previously showed that constitutional 3' end deletions of EPCAM can cause Lynch syndrome through epigenetic silencing of MSH2 in EPCAM-expressing tissues, resulting in tissue-specific MSH2 deficiency.
|
21145788 |
2011 |
Hereditary Nonpolyposis Colorectal Cancer
|
0.700 |
GeneticVariation
|
disease |
BEFREE |
The ultimate diagnosis of Lynch syndrome requires documentation of mutation within one of the four MMR genes (MLH1, PMS2, MSH2 and MSH6) or EPCAM, currently achieved by comprehensive sequencing analysis of germline DNA.
|
26895074 |
2016 |
Hereditary Nonpolyposis Colorectal Cancer
|
0.700 |
AlteredExpression
|
disease |
BEFREE |
Germline deletion of the 3' portion of the Epithelial Cell Adhesion Molecule (EPCAM) gene located 5' upstream of MutS Homolog 2 (MSH2) is a novel mechanism for its inactivation in Lynch syndrome.
|
26613680 |
2016 |
Hereditary Nonpolyposis Colorectal Cancer
|
0.700 |
GeneticVariation
|
disease |
BEFREE |
Heritable somatic methylation and inactivation of MSH2 in families with Lynch syndrome due to deletion of the 3' exons of TACSTD1.
|
19098912 |
2009 |
Hereditary Nonpolyposis Colorectal Cancer
|
0.700 |
GeneticVariation
|
disease |
BEFREE |
Out of the 11 patients, 9 (0.7%) were finally diagnosed as having Lynch syndrome; the responsible genes included MLH1 (n = 1), MSH2 (n = 4), EPCAM (n = 1) and MSH6 (n = 3).
|
27920101 |
2017 |
Hereditary Nonpolyposis Colorectal Cancer
|
0.700 |
GeneticVariation
|
disease |
BEFREE |
Using data from the Colon Cancer Family Registry, we compared the proportion of childhood cancers (diagnosed before 18 years of age) in the first-, second-, and third-degree relatives of 781 probands with a pathogenic mutation in one of the MMR genes; MLH1 (n = 275), MSH2 (n = 342), MSH6 (n = 99), or PMS2 (n = 55) or in EPCAM (n = 10) (Lynch syndrome families), with that of 5073 probands with MMR-deficient colorectal cancer (non-Lynch syndrome families).
|
25963852 |
2015 |
Hereditary Nonpolyposis Colorectal Cancer
|
0.700 |
GeneticVariation
|
disease |
BEFREE |
Lynch syndrome is a hereditary cancer syndrome associated with high risks of colorectal and endometrial cancer that is caused by pathogenic variants in the mismatch repair genes (MLH1, MSH2, MSH6, PMS2, EPCAM).
|
27363726 |
2016 |
Hereditary Nonpolyposis Colorectal Cancer
|
0.700 |
AlteredExpression
|
disease |
BEFREE |
Our study's aim was to explore EPCAM expression in colorectal carcinomas of MSH2-associated LS cases to evaluate the usefulness of EPCAM protein expression in the algorithm approach to LS population screening.
|
23026194 |
2013 |
Hereditary Nonpolyposis Colorectal Cancer
|
0.700 |
GeneticVariation
|
disease |
BEFREE |
Genetic counseling and germline analysis for mutations in genes associated with Lynch syndrome (MLH1, MSH2, MSH6, PMS2, and EPCAM) were offered to individuals with PREMM<sub>1,2,6</sub> scores of 5% or higher.
|
28668538 |
2018 |
Hereditary Nonpolyposis Colorectal Cancer
|
0.700 |
GeneticVariation
|
disease |
BEFREE |
The 138 analyzable patients were all proven mismatch repair mutation carriers for LS (MLH1 = 33%, MSH2 = 47%, MSH6 = 15%, PMS2 = 4%, and EPCAM = 1%).
|
31498154 |
2019 |
Hereditary Nonpolyposis Colorectal Cancer
|
0.700 |
GeneticVariation
|
disease |
BEFREE |
We have recently reported that lack of EPCAM expression occurs in many, but not all tumors from Lynch syndrome patients with EPCAM germline deletions.
|
22388758 |
2012 |
Hereditary Nonpolyposis Colorectal Cancer
|
0.700 |
GeneticVariation
|
disease |
BEFREE |
Cytoplasmic MSH2 immunoreactivity in a patient with Lynch syndrome with an EPCAM-MSH2 fusion.
|
27896849 |
2017 |
Hereditary Nonpolyposis Colorectal Cancer
|
0.700 |
AlteredExpression
|
disease |
BEFREE |
Immunohistochemistry was used to assess EPCAM expression in Lynch syndrome-associated MSH2-negative tumors (n = 26).
|
21115857 |
2011 |
Hereditary Nonpolyposis Colorectal Cancer
|
0.700 |
GeneticVariation
|
disease |
BEFREE |
Larger numbers of Lynch syndrome families and screening of the two additional predisposition genes, PMS2 and EPCAM, are needed in order to decipher the full spectrum of mutations associated with Lynch syndrome predisposition in Cyprus.
|
25133505 |
2014 |
Hereditary Nonpolyposis Colorectal Cancer
|
0.700 |
GeneticVariation
|
disease |
BEFREE |
Recent studies have shown that some Lynch syndrome cases are due to 3' EPCAM/TACSTD1 deletions that subsequently lead to MSH2 promoter hypermethylation.
|
21227399 |
2011 |
Hereditary Nonpolyposis Colorectal Cancer
|
0.700 |
GeneticVariation
|
disease |
BEFREE |
EPCAM germline and somatic rearrangements in Lynch syndrome: identification of a novel 3'EPCAM deletion.
|
23801599 |
2013 |
Hereditary Nonpolyposis Colorectal Cancer
|
0.700 |
GeneticVariation
|
disease |
BEFREE |
Moreover, the mutations in the EpCAM gene lead to congenital tufting enteropathy, severe intestinal epithelium homeostasis disorders, and Lynch and Lynch syndrome.
|
30628064 |
2019 |
Hereditary Nonpolyposis Colorectal Cancer
|
0.700 |
GeneticVariation
|
disease |
BEFREE |
The genetic basis for hereditary nonpolyposis colorectal cancer is the detection of mutations in the MLH1, MSH2, MSH6, PMS2, and EPCAM genes.
|
29776633 |
2018 |
Hereditary Nonpolyposis Colorectal Cancer
|
0.700 |
GeneticVariation
|
disease |
BEFREE |
Being located immediately upstream of the MSH2 gene, EPCAM abnormalities can affect MSH2 and cause Lynch syndrome.
|
31273487 |
2019 |
Hereditary Nonpolyposis Colorectal Cancer
|
0.700 |
GeneticVariation
|
disease |
BEFREE |
The identification of an EPCAM founder mutation has useful implications for the molecular diagnosis of LS in Spain.
|
23530899 |
2014 |
Hereditary Nonpolyposis Colorectal Cancer
|
0.700 |
GeneticVariation
|
disease |
BEFREE |
Next to mutations c. 2041G>A in MLH1 gene and c.942+3A>T in MSH2, the deletion mutation encompassing EPCAM is one of the most common causative changes responsible for LS in Poland.
|
28369810 |
2017 |
Hereditary Nonpolyposis Colorectal Cancer
|
0.700 |
GeneticVariation
|
disease |
BEFREE |
Toward a better definition of EPCAM deletions in Lynch Syndrome: Report of new variants in Italy and the associated molecular phenotype.
|
30916491 |
2019 |
Hereditary Nonpolyposis Colorectal Cancer
|
0.700 |
GeneticVariation
|
disease |
BEFREE |
It was recently shown that constitutional 3' end deletions of EPCAM could cause Lynch syndrome in tissues with MSH2 deficiency.
|
21791569 |
2011 |
Hereditary Nonpolyposis Colorectal Cancer
|
0.700 |
GeneticVariation
|
disease |
BEFREE |
EPCAM deletion analysis followed by MSH2 methylation testing of the tumor is a fast low-cost procedure that can be used to identify mutations that cause LS.
|
20864635 |
2010 |
Hereditary Nonpolyposis Colorectal Cancer
|
0.700 |
Biomarker
|
disease |
BEFREE |
We developed a new prediction model, PREMM<sub>5</sub>, that incorporates the genes PMS2 and EPCAM to provide comprehensive LS risk assessment.
|
28489507 |
2017 |