Malignant neoplasm of prostate
|
0.380 |
Biomarker
|
disease |
BEFREE |
Further secondary and tertiary hit characterization assays are underway to select AR-TIF2 PPI inhibitor/disruptor hits suitable for medicinal chemistry lead optimization and development into novel PCa/CRPC therapeutics.
|
30109944 |
2019 |
Malignant neoplasm of prostate
|
0.380 |
Biomarker
|
disease |
BEFREE |
Furthermore, for the first time, we detected a structural rearrangement involving NCOA2 in PCa.
|
26799514 |
2016 |
Malignant neoplasm of prostate
|
0.380 |
Biomarker
|
disease |
BEFREE |
Concordant assessment of DNA copy number, mRNA expression, and focused exon resequencing in 218 prostate cancer tumors identified the nuclear receptor coactivator NCOA2 as an oncogene in approximately 11% of tumors.
|
20579941 |
2010 |
Malignant neoplasm of prostate
|
0.380 |
Biomarker
|
disease |
BEFREE |
Interleukin-6 increases prostate cancer cells resistance to bicalutamide via TIF2.
|
19240160 |
2009 |
Malignant neoplasm of prostate
|
0.380 |
AlteredExpression
|
disease |
BEFREE |
Depletion of TIF2 reduced expression of AR-induced target genes and slowed proliferation of AR-dependent and AR-independent prostate cancer cells.
|
17079484 |
2006 |
Malignant neoplasm of prostate
|
0.380 |
AlteredExpression
|
disease |
BEFREE |
Cofactors SRC-1, RAC3, p300/CBP, TIF-2, and Tip60 are upregulated in advanced prostate cancer.
|
16598769 |
2006 |
Malignant neoplasm of prostate
|
0.380 |
AlteredExpression
|
disease |
BEFREE |
AR coactivators SRC-1 and TIF-2 are up-regulated in tissue specimens obtained from patients who failed prostate cancer endocrine therapy.
|
15663989 |
2004 |
Malignant neoplasm of prostate
|
0.380 |
Biomarker
|
disease |
CTD_human |
The three coactivators, TIF-2, SRC-1 and RAC3, are up-regulated in relapsed prostate cancer.
|
12237244 |
2002 |
Malignant neoplasm of prostate
|
0.380 |
AlteredExpression
|
disease |
BEFREE |
The three coactivators, TIF-2, SRC-1 and RAC3, are up-regulated in relapsed prostate cancer.
|
12237244 |
2002 |
Malignant neoplasm of breast
|
0.360 |
Biomarker
|
disease |
BEFREE |
However, the transcriptional role of SRC-2 in breast cancer is still ambiguous.
|
30048685 |
2019 |
Malignant neoplasm of breast
|
0.360 |
Biomarker
|
disease |
BEFREE |
In conclusion, our results suggest NCOA2 as a potential target of therapeutics against breast cancer.
|
30941313 |
2019 |
Breast Carcinoma
|
0.360 |
Biomarker
|
disease |
BEFREE |
However, the transcriptional role of SRC-2 in breast cancer is still ambiguous.
|
30048685 |
2019 |
Breast Carcinoma
|
0.360 |
Biomarker
|
disease |
BEFREE |
In conclusion, our results suggest NCOA2 as a potential target of therapeutics against breast cancer.
|
30941313 |
2019 |
Malignant neoplasm of breast
|
0.360 |
AlteredExpression
|
disease |
BEFREE |
As the members of the p160/nuclear receptor co-activator (NCOA) family, NCOA1, NCOA2 and NCOA3 are known to be overexpressed in breast cancer and essentially involved in estrogen-mediated cancer cell proliferation we asked if these proteins are involved in the ERα-mediated transactivation of PLAC1 in breast cancer cells.
|
24304549 |
2013 |
Breast Carcinoma
|
0.360 |
AlteredExpression
|
disease |
BEFREE |
As the members of the p160/nuclear receptor co-activator (NCOA) family, NCOA1, NCOA2 and NCOA3 are known to be overexpressed in breast cancer and essentially involved in estrogen-mediated cancer cell proliferation we asked if these proteins are involved in the ERα-mediated transactivation of PLAC1 in breast cancer cells.
|
24304549 |
2013 |
Malignant neoplasm of breast
|
0.360 |
Biomarker
|
disease |
BEFREE |
Collectively, these data indicate that SRC control of basal and hormone-regulated proliferations is not solely mediated by ERα, and suggest that targeting growth inhibition by disrupting SRC-2 and SRC-3 function may be an effective approach to inhibit the growth of tamoxifen-resistant breast cancer.
|
21059860 |
2011 |
Breast Carcinoma
|
0.360 |
Biomarker
|
disease |
BEFREE |
Collectively, these data indicate that SRC control of basal and hormone-regulated proliferations is not solely mediated by ERα, and suggest that targeting growth inhibition by disrupting SRC-2 and SRC-3 function may be an effective approach to inhibit the growth of tamoxifen-resistant breast cancer.
|
21059860 |
2011 |
Malignant neoplasm of breast
|
0.360 |
Biomarker
|
disease |
CTD_human |
Effect of low-dose tamoxifen on steroid receptor coactivator 3/amplified in breast cancer 1 in normal and malignant human breast tissue.
|
20332317 |
2010 |
Malignant neoplasm of breast
|
0.360 |
Biomarker
|
disease |
BEFREE |
Genes of known importance in breast cancer and estrogen signaling, including ERBB2, PGR, MYC, CLU, and NCOA2, were among those identified as Sin3A-responsive.
|
20920219 |
2010 |
Breast Carcinoma
|
0.360 |
Biomarker
|
disease |
CTD_human |
Effect of low-dose tamoxifen on steroid receptor coactivator 3/amplified in breast cancer 1 in normal and malignant human breast tissue.
|
20332317 |
2010 |
Breast Carcinoma
|
0.360 |
Biomarker
|
disease |
BEFREE |
Genes of known importance in breast cancer and estrogen signaling, including ERBB2, PGR, MYC, CLU, and NCOA2, were among those identified as Sin3A-responsive.
|
20920219 |
2010 |
Malignant neoplasm of breast
|
0.360 |
AlteredExpression
|
disease |
BEFREE |
Amplified in breast cancer (AIB1 or SRC-3) is an estrogen receptor coregulatory protein that together with other co-activators like transcription intermediary factor 2 (TIF2) and nuclear receptor co-repressor (NCoR), is implicated in estrogen signaling pathway and estrogen regulated tumor progression.
|
18521745 |
2009 |
Breast Carcinoma
|
0.360 |
AlteredExpression
|
disease |
BEFREE |
Amplified in breast cancer (AIB1 or SRC-3) is an estrogen receptor coregulatory protein that together with other co-activators like transcription intermediary factor 2 (TIF2) and nuclear receptor co-repressor (NCoR), is implicated in estrogen signaling pathway and estrogen regulated tumor progression.
|
18521745 |
2009 |
Mammary Neoplasms
|
0.320 |
Biomarker
|
group |
BEFREE |
Elevated expression of steroid receptor coactivator-3 (SRC-3), a member of the p160 family of nuclear receptor coactivators, has been implicated in tamoxifen resistance of breast tumors while the involvement of the two other members of this family, SRC-1 and SRC-2, is less well characterized.
|
21059860 |
2011 |
Mammary Neoplasms
|
0.320 |
Biomarker
|
group |
CTD_human |
Effect of low-dose tamoxifen on steroid receptor coactivator 3/amplified in breast cancer 1 in normal and malignant human breast tissue.
|
20332317 |
2010 |