Malignant neoplasm of breast
|
0.060 |
GeneticVariation
|
disease |
BEFREE |
A novel RAP80 haplotype or rare missense mutations may be associated with a modest increased risk of breast cancer, but this observation needs to be confirmed by additional studies.
|
18306035 |
2009 |
Malignant neoplasm of breast
|
0.060 |
GeneticVariation
|
disease |
BEFREE |
Conclusions Overall, it seems unlikely that moderate to highly penetrant alleles of either RAP80 or Abraxas, confer a significantly high relative risk of breast cancer.
|
18695986 |
2009 |
Malignant neoplasm of breast
|
0.060 |
Biomarker
|
disease |
BEFREE |
Our analysis suggests that RAP80 and CCDC98 do not play an important role as high penetrance breast cancer susceptibility genes.
|
18270812 |
2009 |
Malignant neoplasm of breast
|
0.060 |
AlteredExpression
|
disease |
BEFREE |
Association between the epithelial growth factor receptor (EGFR) mutation and the expression of breast cancer 1 (BRCA1) and receptor-associated protein 80 (RAP80) in non-small cell lung cancer (NSCLC) was studied.
|
30008919 |
2018 |
Malignant neoplasm of breast
|
0.060 |
Biomarker
|
disease |
BEFREE |
Mutation screening of the MERIT40 gene encoding a novel BRCA1 and RAP80 interacting protein in breast cancer families.
|
19572197 |
2010 |
Malignant neoplasm of breast
|
0.060 |
AlteredExpression
|
disease |
BEFREE |
RAP80 expression in breast cancer (62.3%, 101/162) was significantly lower than that in adjacent normal breast tissues (<i>P</i><0.05).
|
30705591 |
2019 |
Breast Carcinoma
|
0.060 |
AlteredExpression
|
disease |
BEFREE |
Association between the epithelial growth factor receptor (EGFR) mutation and the expression of breast cancer 1 (BRCA1) and receptor-associated protein 80 (RAP80) in non-small cell lung cancer (NSCLC) was studied.
|
30008919 |
2018 |
Breast Carcinoma
|
0.060 |
Biomarker
|
disease |
BEFREE |
Our analysis suggests that RAP80 and CCDC98 do not play an important role as high penetrance breast cancer susceptibility genes.
|
18270812 |
2009 |
Breast Carcinoma
|
0.060 |
GeneticVariation
|
disease |
BEFREE |
A novel RAP80 haplotype or rare missense mutations may be associated with a modest increased risk of breast cancer, but this observation needs to be confirmed by additional studies.
|
18306035 |
2009 |
Breast Carcinoma
|
0.060 |
GeneticVariation
|
disease |
BEFREE |
Conclusions Overall, it seems unlikely that moderate to highly penetrant alleles of either RAP80 or Abraxas, confer a significantly high relative risk of breast cancer.
|
18695986 |
2009 |
Breast Carcinoma
|
0.060 |
Biomarker
|
disease |
BEFREE |
Mutation screening of the MERIT40 gene encoding a novel BRCA1 and RAP80 interacting protein in breast cancer families.
|
19572197 |
2010 |
Breast Carcinoma
|
0.060 |
AlteredExpression
|
disease |
BEFREE |
RAP80 expression in breast cancer (62.3%, 101/162) was significantly lower than that in adjacent normal breast tissues (<i>P</i><0.05).
|
30705591 |
2019 |
Non-Small Cell Lung Carcinoma
|
0.030 |
AlteredExpression
|
disease |
BEFREE |
Tubulin, BRCA1, ERCC1, Abraxas, RAP80 mRNA expression, p53/p21 immunohistochemistry and clinical outcome in patients with advanced non small-cell lung cancer receiving first-line platinum-gemcitabine chemotherapy.
|
21529986 |
2011 |
Non-Small Cell Lung Carcinoma
|
0.030 |
AlteredExpression
|
disease |
BEFREE |
The protein fluorescence expression of BRCA1 and RAP80 in non-small cell lung cancer group was significantly increased.
|
30008919 |
2018 |
Non-Small Cell Lung Carcinoma
|
0.030 |
AlteredExpression
|
disease |
BEFREE |
In a Spanish Lung Cancer Group (SLCG) phase II trial, the combination of BRCA1 and receptor-associated protein 80 (RAP80) expression was significantly associated with outcome in Caucasian patients with nonsmall-cell lung cancer (NSCLC).
|
25164908 |
2014 |
Breast Cancer, Familial
|
0.020 |
GeneticVariation
|
disease |
BEFREE |
In summary, we did not find truncating mutations of the RAP80 gene to be a cause of familial breast cancer.
|
18306035 |
2009 |
Breast Cancer, Familial
|
0.020 |
GeneticVariation
|
disease |
BEFREE |
Evaluation of the BRCA1 interacting genes RAP80 and CCDC98 in familial breast cancer susceptibility.
|
18270812 |
2009 |
Fanconi Anemia
|
0.010 |
Biomarker
|
disease |
BEFREE |
These findings implicate MERIT40 in the earliest stages of ICL repair and define specific functional interactions between RAP80 complex-dependent ubiquitin recognition and the Fanconi anemia (FA)-BRCA ICL repair network.
|
26338419 |
2015 |
Ovarian Carcinoma
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
Low RAP80 mRNA expression correlates with shorter survival in sporadic high-grade serous ovarian carcinoma.
|
27443420 |
2017 |
Squamous cell carcinoma of esophagus
|
0.010 |
Biomarker
|
disease |
BEFREE |
Moreover, the RAP80 mRNA level was validated to be an independent prognosis biomarker for the overall survival time of ESCC patients.
|
29396516 |
2018 |
ovarian neoplasm
|
0.010 |
GeneticVariation
|
disease |
LHGDN |
Evaluation of the BRCA1 interacting genes RAP80 and CCDC98 in familial breast cancer susceptibility.
|
18270812 |
2009 |
Malignant neoplasm of ovary
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
Low RAP80 mRNA expression correlates with shorter survival in sporadic high-grade serous ovarian carcinoma.
|
27443420 |
2017 |
Sporadic Breast Carcinoma
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
BRCA1 PARsylation and/or RAP80 expression is defective in a subset of sporadic breast cancer cell lines and patient-derived tumor xenograft models.
|
25252691 |
2014 |
FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder)
|
0.010 |
Biomarker
|
disease |
BEFREE |
These findings implicate MERIT40 in the earliest stages of ICL repair and define specific functional interactions between RAP80 complex-dependent ubiquitin recognition and the Fanconi anemia (FA)-BRCA ICL repair network.
|
26338419 |
2015 |
Triple Negative Breast Neoplasms
|
0.010 |
GeneticVariation
|
disease |
BEFREE |
We detected 37 common variants in ABRAXAS, RAP80, BRE, BRCC36 and NBA1/MERIT40 genes encoding the BRCA1-A complex and evaluated their genetic susceptibility to the risk of TNBC.
|
26848770 |
2016 |