Neoplasms
|
0.080 |
AlteredExpression
|
group |
BEFREE |
DAC can restore expression of NALP1 to suppress tumor growth in colon cancer.
|
25611377 |
2015 |
Malignant neoplasm of lung
|
0.010 |
Biomarker
|
disease |
BEFREE |
DAC (5-aza-2-deoxycytidine) is an antitumor drug useful to lung cancer, myelodysplastic disorders, myelodysplasia and acute myeloid leukemia.
|
25611377 |
2015 |
Carcinoma of lung
|
0.010 |
Biomarker
|
disease |
BEFREE |
DAC (5-aza-2-deoxycytidine) is an antitumor drug useful to lung cancer, myelodysplastic disorders, myelodysplasia and acute myeloid leukemia.
|
25611377 |
2015 |
Primary malignant neoplasm of lung
|
0.010 |
Biomarker
|
disease |
BEFREE |
DAC (5-aza-2-deoxycytidine) is an antitumor drug useful to lung cancer, myelodysplastic disorders, myelodysplasia and acute myeloid leukemia.
|
25611377 |
2015 |
MYELODYSPLASTIC SYNDROME
|
0.060 |
Biomarker
|
group |
BEFREE |
DAC (5-aza-2-deoxycytidine) is an antitumor drug useful to lung cancer, myelodysplastic disorders, myelodysplasia and acute myeloid leukemia.
|
25611377 |
2015 |
Myelodysplasia
|
0.030 |
Biomarker
|
disease |
BEFREE |
DAC (5-aza-2-deoxycytidine) is an antitumor drug useful to lung cancer, myelodysplastic disorders, myelodysplasia and acute myeloid leukemia.
|
25611377 |
2015 |
Leukemia, Myelocytic, Acute
|
0.090 |
Biomarker
|
disease |
BEFREE |
DAC (5-aza-2-deoxycytidine) is an antitumor drug useful to lung cancer, myelodysplastic disorders, myelodysplasia and acute myeloid leukemia.
|
25611377 |
2015 |
Gilles de la Tourette syndrome
|
0.020 |
Biomarker
|
disease |
BEFREE |
AADAC is a candidate susceptibility factor for GTS and the present findings warrant further genomic and functional studies to investigate the role of this gene in the pathogenesis of GTS.
|
26444075 |
2016 |
Multiple Sclerosis, Relapsing-Remitting
|
0.020 |
Biomarker
|
disease |
BEFREE |
A comprehensive clinical program in relapsing-remitting multiple sclerosis demonstrated an impressive effect of DAC-HYP on inflammatory and clinical disease activity compared with placebo or interferon beta, which led to its recent approval for the treatment of relapsing forms of multiple sclerosis.
|
28387383 |
2017 |
Multiple Sclerosis
|
0.030 |
AlteredExpression
|
disease |
BEFREE |
A comprehensive clinical program in relapsing-remitting multiple sclerosis demonstrated an impressive effect of DAC-HYP on inflammatory and clinical disease activity compared with placebo or interferon beta, which led to its recent approval for the treatment of relapsing forms of multiple sclerosis.
|
28387383 |
2017 |
HIV Infections
|
0.010 |
Biomarker
|
group |
BEFREE |
A Population Pharmacokinetic Analysis Shows that Arylacetamide Deacetylase (AADAC) Gene Polymorphism and HIV Infection Affect the Exposure of Rifapentine.
|
30670438 |
2019 |
Sarcoma
|
0.010 |
AlteredExpression
|
group |
BEFREE |
A significant increase in the mRNA expression levels of MAGE-A1 and MAGE-A3 were found in 70 %, and NY-ESO-1 in 80 % of the sarcoma lines following exposure to pharmacological levels of DAC.
|
24584817 |
2014 |
Malignant neoplasm of soft tissue
|
0.010 |
AlteredExpression
|
group |
BEFREE |
A significant increase in the mRNA expression levels of MAGE-A1 and MAGE-A3 were found in 70 %, and NY-ESO-1 in 80 % of the sarcoma lines following exposure to pharmacological levels of DAC.
|
24584817 |
2014 |
Multiple Sclerosis, Relapsing-Remitting
|
0.020 |
Biomarker
|
disease |
BEFREE |
Continued clinical experience with DAC-beta, including observations from the REMS program, will define its place in the armamentarium of immunotherapeutics for relapsing-remitting multiple sclerosis.
|
28707278 |
2017 |
Neoplasms
|
0.080 |
Biomarker
|
group |
BEFREE |
Cytotoxic T cells specifically recognizing MAGE-A family and NY-ESO-1 clustered at the tumor site in mice pre-treated with DAC and resulted in tumor growth suppression, while it was not observed in mice without DAC pre-treatment.
|
25301731 |
2014 |
Leukemia, Myelocytic, Acute
|
0.090 |
Biomarker
|
disease |
BEFREE |
Decitabine (5-Aza-2'-deoxycytidine, DAC), an anti-leukemic drug, is effective in treating acute myeloid leukemia (AML) and myelodysplastic syndrome (MDS).
|
30210693 |
2018 |
MYELODYSPLASTIC SYNDROME
|
0.060 |
Biomarker
|
group |
BEFREE |
Decitabine (5-Aza-2'-deoxycytidine, DAC), an anti-leukemic drug, is effective in treating acute myeloid leukemia (AML) and myelodysplastic syndrome (MDS).
|
30210693 |
2018 |
MYELODYSPLASTIC SYNDROME
|
0.060 |
Biomarker
|
group |
BEFREE |
During the last 10 years, three European phase II studies were performed to investigate the treatment of elderly patients with myelodysplastic syndrome (MDS) with low-dose 5-aza-2'-deoxycytidine (decitabine, DAC).
|
16211386 |
2005 |
Leukemia, Myelocytic, Acute
|
0.090 |
GeneticVariation
|
disease |
BEFREE |
Early induction intensification with cladribine, cytarabine, and mitoxantrone (CLAM) in AML patients treated with the DAC induction regimen: a prospective, non-randomized, phase II study of the Polish Adult Leukemia Group (PALG).
|
31661339 |
2020 |
Acute monocytic leukemia
|
0.010 |
GeneticVariation
|
disease |
BEFREE |
Early induction intensification with cladribine, cytarabine, and mitoxantrone (CLAM) in AML patients treated with the DAC induction regimen: a prospective, non-randomized, phase II study of the Polish Adult Leukemia Group (PALG).
|
31661339 |
2020 |
MYELODYSPLASTIC SYNDROME
|
0.060 |
GeneticVariation
|
group |
BEFREE |
Encouraging response rates of about 50% in myelodysplasia with 5-azacytidine and 5-aza-2'-deoxycytidine (decitabine or DAC) have resulted in a number of phase III studies being initiated in this disorder.
|
16210092 |
2005 |
Myelodysplasia
|
0.030 |
GeneticVariation
|
disease |
BEFREE |
Encouraging response rates of about 50% in myelodysplasia with 5-azacytidine and 5-aza-2'-deoxycytidine (decitabine or DAC) have resulted in a number of phase III studies being initiated in this disorder.
|
16210092 |
2005 |
Multiple Sclerosis
|
0.030 |
Biomarker
|
disease |
BEFREE |
Expert commentary: Monthly daclizumab-beta [DAC-beta, formerly daclizumab high yield process (DAC HYP), approved as ZINBRYTA®, which has a different form and structure than an earlier form of daclizumab], is an effective and convenient treatment option for patients with relapsing forms of MS who have failed other treatment, or as a first-line option in highly active MS patients.
|
28803486 |
2017 |
Malignant Neoplasms
|
0.030 |
Biomarker
|
group |
BEFREE |
Functional assays, such as flow cytometry, cytotoxicity assays and ELISA, were performed to determine the demethylation agent, decitabine (5-aza-2'-deoxycytidine, DAC)-treated cancer cell improved antigen specific T cells response.
|
30797153 |
2019 |
Primary malignant neoplasm
|
0.020 |
Biomarker
|
group |
BEFREE |
Functional assays, such as flow cytometry, cytotoxicity assays and ELISA, were performed to determine the demethylation agent, decitabine (5-aza-2'-deoxycytidine, DAC)-treated cancer cell improved antigen specific T cells response.
|
30797153 |
2019 |