vorinostat has been researched along with Cancer of the Thyroid in 12 studies
Vorinostat: A hydroxamic acid and anilide derivative that acts as a HISTONE DEACETYLASE inhibitor. It is used in the treatment of CUTANEOUS T-CELL LYMPHOMA and SEZARY SYNDROME.
vorinostat : A dicarboxylic acid diamide comprising suberic (octanedioic) acid coupled to aniline and hydroxylamine. A histone deacetylase inhibitor, it is marketed under the name Zolinza for the treatment of cutaneous T cell lymphoma (CTCL).
Excerpt | Relevance | Reference |
---|---|---|
"The incidence of thyroid cancer continues to increase and this neoplasia remains the most common endocrine malignancy." | 2.48 | Novel molecular targeted therapies for refractory thyroid cancer. ( Arango, BA; Cohen, EE; Perez, CA; Raez, LE; Santos, ES, 2012) |
"In both, thyroid cancer is driven by overactivation of PI3K-AKT signaling." | 1.43 | SAHA-induced loss of tumor suppressor Pten gene promotes thyroid carcinogenesis in a mouse model. ( Cheng, SY; Kim, DW; Willingham, MC; Zhao, L; Zhu, X, 2016) |
"Seven thyroid cancer cell lines (SNU-790, BCPAP, KTC1, TPC1, TPC1-M, KTC2, and FRO) and four HIF1α inhibitors (echinomycin, LAQ824, temsirolimus, and vorinostat) were used in the present study." | 1.42 | Effect of perioperative treatment with a hypoxia-inducible factor-1-alpha inhibitor in an orthotopic surgical mouse model of thyroid cancer. ( Ahn, SH; Cha, W; Jeon, EH; Jeong, WJ; Kim, DW; Kim, SD, 2015) |
" The objective of this study was to investigate the effects of 1,25(OH)(2)D(3) and the superagonistic analog CD578 in anaplastic thyroid cancer, alone or in combination with paclitaxel, a taxane, and suberoylanilide hydroxamic acid (SAHA), a potent histone deacetylase inhibitor with promising effects in undifferentiated thyroid cancer." | 1.37 | 1,25-dihydroxyvitamin D3 and a superagonistic analog in combination with paclitaxel or suberoylanilide hydroxamic acid have potent antiproliferative effects on anaplastic thyroid cancer. ( Bouillon, R; Clinckspoor, I; Decallonne, B; Korch, C; Mathieu, C; Overbergh, L; Verlinden, L; Verstuyf, A, 2011) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 4 (33.33) | 29.6817 |
2010's | 8 (66.67) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Cha, W | 1 |
Kim, DW | 2 |
Kim, SD | 1 |
Jeon, EH | 1 |
Jeong, WJ | 1 |
Ahn, SH | 1 |
Kim, SH | 1 |
Kang, JG | 1 |
Kim, CS | 1 |
Ihm, SH | 1 |
Choi, MG | 1 |
Yoo, HJ | 1 |
Lee, SJ | 1 |
Zhu, X | 1 |
Zhao, L | 1 |
Willingham, MC | 1 |
Cheng, SY | 1 |
Ning, L | 1 |
Jaskula-Sztul, R | 1 |
Kunnimalaiyaan, M | 1 |
Chen, H | 1 |
Woyach, JA | 1 |
Kloos, RT | 1 |
Ringel, MD | 1 |
Arbogast, D | 1 |
Collamore, M | 1 |
Zwiebel, JA | 1 |
Grever, M | 1 |
Villalona-Calero, M | 1 |
Shah, MH | 1 |
Borbone, E | 1 |
Berlingieri, MT | 1 |
De Bellis, F | 1 |
Nebbioso, A | 1 |
Chiappetta, G | 1 |
Mai, A | 1 |
Altucci, L | 1 |
Fusco, A | 1 |
Hou, P | 1 |
Bojdani, E | 1 |
Xing, M | 1 |
Clinckspoor, I | 1 |
Verlinden, L | 1 |
Overbergh, L | 1 |
Korch, C | 1 |
Bouillon, R | 1 |
Mathieu, C | 1 |
Verstuyf, A | 1 |
Decallonne, B | 1 |
Perez, CA | 1 |
Santos, ES | 1 |
Arango, BA | 1 |
Raez, LE | 1 |
Cohen, EE | 1 |
Dom, G | 1 |
Galdo, VC | 1 |
Tarabichi, M | 1 |
Tomás, G | 1 |
Hébrant, A | 1 |
Andry, G | 1 |
De Martelar, V | 1 |
Libert, F | 1 |
Leteurtre, E | 1 |
Dumont, JE | 1 |
Maenhaut, C | 1 |
van Staveren, WC | 1 |
Mitsiades, CS | 1 |
Poulaki, V | 1 |
McMullan, C | 1 |
Negri, J | 1 |
Fanourakis, G | 1 |
Goudopoulou, A | 1 |
Richon, VM | 1 |
Marks, PA | 1 |
Mitsiades, N | 1 |
Luong, QT | 1 |
O'Kelly, J | 1 |
Braunstein, GD | 1 |
Hershman, JM | 1 |
Koeffler, HP | 1 |
Trial | Phase | Enrollment | Study Type | Start Date | Status | ||
---|---|---|---|---|---|---|---|
Phase II Study of Histone Deacetylase Inhibitor SAHA (Vorinostat) in Patients With Metastatic Thyroid Carcinoma[NCT00134043] | Phase 2 | 19 participants (Actual) | Interventional | 2005-12-31 | Completed | ||
[information is prepared from clinicaltrials.gov, extracted Sep-2024] |
"Per Response Evaluation Criteria In Solid Tumors Criteria (RECIST v1.0) for target lesions and assessed by MRI: Complete Response (CR), Disappearance of all target lesions; Partial Response (PR), >=30% decrease in the sum of the longest diameter of target lesions; Overall Response (OR) = CR + PR., or similar definition that is accurate and appropriate." (NCT00134043)
Timeframe: Up to 3 years
Intervention | percentage of participants (Number) | ||
---|---|---|---|
PR (Partial Response) | CR (Complete Response) | Stable disease | |
DTCs (Well-differentiated Thyroid Carcinomas) | 0 | 0 | 56 |
MTC (Medullary Thyroid Cancer) | 0 | 0 | 0 |
1 review available for vorinostat and Cancer of the Thyroid
Article | Year |
---|---|
Novel molecular targeted therapies for refractory thyroid cancer.
Topics: Angiogenesis Inhibitors; Anilides; Antineoplastic Agents; Axitinib; Benzamides; Benzenesulfonates; B | 2012 |
1 trial available for vorinostat and Cancer of the Thyroid
Article | Year |
---|---|
Lack of therapeutic effect of the histone deacetylase inhibitor vorinostat in patients with metastatic radioiodine-refractory thyroid carcinoma.
Topics: Adult; Aged; Antineoplastic Agents; Calcitonin; Carcinoembryonic Antigen; Carcinoma, Medullary; Enzy | 2009 |
10 other studies available for vorinostat and Cancer of the Thyroid
Article | Year |
---|---|
Effect of perioperative treatment with a hypoxia-inducible factor-1-alpha inhibitor in an orthotopic surgical mouse model of thyroid cancer.
Topics: Animals; Apoptosis; Cell Proliferation; Disease Models, Animal; Gene Expression Regulation, Neoplast | 2015 |
The heat shock protein 90 inhibitor SNX5422 has a synergistic activity with histone deacetylase inhibitors in induction of death of anaplastic thyroid carcinoma cells.
Topics: Antineoplastic Agents; Apoptosis; Benzamides; Caspase 3; Cell Line, Tumor; Cell Survival; Drug Syner | 2016 |
SAHA-induced loss of tumor suppressor Pten gene promotes thyroid carcinogenesis in a mouse model.
Topics: Adenocarcinoma, Follicular; Animals; Carcinogenesis; Disease Models, Animal; Hydroxamic Acids; Mice, | 2016 |
Suberoyl bishydroxamic acid activates notch1 signaling and suppresses tumor progression in an animal model of medullary thyroid carcinoma.
Topics: Animals; Apoptosis; Basic Helix-Loop-Helix Transcription Factors; Blotting, Western; Carcinoma, Medu | 2008 |
Histone deacetylase inhibitors induce thyroid cancer-specific apoptosis through proteasome-dependent inhibition of TRAIL degradation.
Topics: Animals; Apoptosis; Benzamides; Blotting, Western; Carcinoma; Cell Line; Cell Line, Tumor; Cell Prol | 2010 |
Induction of thyroid gene expression and radioiodine uptake in thyroid cancer cells by targeting major signaling pathways.
Topics: Cell Line, Tumor; Gene Expression Regulation; Humans; Hydroxamic Acids; Intracellular Signaling Pept | 2010 |
1,25-dihydroxyvitamin D3 and a superagonistic analog in combination with paclitaxel or suberoylanilide hydroxamic acid have potent antiproliferative effects on anaplastic thyroid cancer.
Topics: Antineoplastic Combined Chemotherapy Protocols; Calcitriol; Cell Cycle; Cell Line, Tumor; Cell Proli | 2011 |
5-aza-2'-deoxycytidine has minor effects on differentiation in human thyroid cancer cell lines, but modulates genes that are involved in adaptation in vitro.
Topics: Antimetabolites, Antineoplastic; Apoptosis; Azacitidine; Carcinoma; Cell Differentiation; Cell Line, | 2013 |
Novel histone deacetylase inhibitors in the treatment of thyroid cancer.
Topics: Antineoplastic Agents; Apoptosis; Carcinoma; Cell Death; Cinnamates; Down-Regulation; Gene Expressio | 2005 |
Antitumor activity of suberoylanilide hydroxamic acid against thyroid cancer cell lines in vitro and in vivo.
Topics: Animals; Antineoplastic Agents; Apoptosis Regulatory Proteins; Carboplatin; Carcinoma; Cell Cycle Pr | 2006 |