Page last updated: 2024-10-26

valproic acid and Carcinoma, Non-Small Cell Lung

valproic acid has been researched along with Carcinoma, Non-Small Cell Lung in 15 studies

Valproic Acid: A fatty acid with anticonvulsant and anti-manic properties that is used in the treatment of EPILEPSY and BIPOLAR DISORDER. The mechanisms of its therapeutic actions are not well understood. It may act by increasing GAMMA-AMINOBUTYRIC ACID levels in the brain or by altering the properties of VOLTAGE-GATED SODIUM CHANNELS.
valproic acid : A branched-chain saturated fatty acid that comprises of a propyl substituent on a pentanoic acid stem.

Research Excerpts

ExcerptRelevanceReference
" Patients were treated with escalating doses of decitabine (5-15 mg/m(2)) IV for 10 days in combination with VPA (10-20 mg/kg/day) PO on days 5-21 of a 28-day cycle."2.78Phase I study of 5-aza-2'-deoxycytidine in combination with valproic acid in non-small-cell lung cancer. ( Aimiuwu, J; Chan, KK; Chu, BF; Grever, MR; Karpenko, MJ; Liu, Z; Otterson, GA; Villalona-Calero, MA, 2013)
"Lung cancer is the most frequent cause of cancer death."1.72Tumors derived from lung cancer cells respond differently to treatment with sodium valproate (a HDAC inhibitor) in a chicken embryo chorioallantoic membrane model. ( Balnytė, I; Diržiuvienė, R; Lasienė, K; Palubinskienė, J; Šlekienė, L; Stakišaitis, D; Valančiūtė, A, 2022)
" In this paper, we have investigated the cytotoxic interaction of ERL and valproic acid (VA) in ERL-resistant NSCLC cells and developed a liquisolid formulation of ERL-VA for improving oral bioavailability of ERL."1.51Erlotinib-Valproic Acid Liquisolid Formulation: Evaluating Oral Bioavailability and Cytotoxicity in Erlotinib-Resistant Non-small Cell Lung Cancer Cells. ( Bagde, A; Doddapaneni, R; Patel, K; Patki, M; Sekar, V; Singh, M, 2019)
"Valproic acid (VPA) has been suggested to be a histone deacetylase inhibitor (HDACI)."1.46Valproic acid (VPA) enhances cisplatin sensitivity of non-small cell lung cancer cells via HDAC2 mediated down regulation of ABCA1. ( Chen, JH; Ding, ZL; Fu, R; Gu, LZ; Hu, CP; Qin, L; Wan, YF; Wang, Y; Xu, CQ; Zheng, YL, 2017)
" Oral dosing of mice results in absorption of intact prodrug with slow systemic hydrolysis yielding higher plasma levels of LY2334737 than gemcitabine and prolonged gemcitabine exposure."1.39Efficacy of low-dose oral metronomic dosing of the prodrug of gemcitabine, LY2334737, in human tumor xenografts. ( Dantzig, AH; Donoho, GP; Durland-Busbice, S; Perkins, EJ; Pratt, SE; Shepard, RL; Starling, JJ; Wickremsinhe, ER, 2013)
" The abovementioned activity of VPA as a differentiation agent suggested that it might be worth investigating its possible therapeutic potential in synergistic combination with FTS."1.37Downregulation of survivin and aurora A by histone deacetylase and RAS inhibitors: a new drug combination for cancer therapy. ( Biran, A; Brownstein, M; Haklai, R; Kloog, Y, 2011)

Research

Studies (15)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (6.67)29.6817
2010's13 (86.67)24.3611
2020's1 (6.67)2.80

Authors

AuthorsStudies
Diržiuvienė, R1
Šlekienė, L1
Palubinskienė, J1
Balnytė, I1
Lasienė, K1
Stakišaitis, D1
Valančiūtė, A1
Patel, K1
Doddapaneni, R1
Patki, M1
Sekar, V1
Bagde, A1
Singh, M1
Du, XZ1
Li, QY1
Du, FW1
He, ZG1
Wang, J1
Shirsath, N1
Rathos, M1
Chaudhari, U1
Sivaramakrishnan, H1
Joshi, K1
Gavrilov, V1
Lavrenkov, K1
Ariad, S1
Shany, S1
Ciardiello, C1
Roca, MS1
Noto, A1
Bruzzese, F1
Moccia, T1
Vitagliano, C1
Di Gennaro, E1
Ciliberto, G1
Roscilli, G1
Aurisicchio, L1
Marra, E1
Mancini, R1
Budillon, A1
Leone, A1
Carter, CA1
Zeman, K1
Day, RM1
Richard, P1
Oronsky, A1
Oronsky, N1
Lybeck, M1
Scicinski, J1
Oronsky, B1
Aebischer, B1
Elsig, S1
Taeymans, J1
Pomp, S1
Kuhness, D1
Barcaro, G1
Sementa, L1
Mankad, V1
Fortunelli, A1
Sterrer, M1
Netzer, FP1
Surnev, S1
Schmieder, AH1
Caruthers, SD1
Keupp, J1
Wickline, SA1
Lanza, GM1
Lowe, J1
Wodarcyk, AJ1
Floyd, KT1
Rastogi, N1
Schultz, EJ1
Swager, SA1
Chadwick, JA1
Tran, T1
Raman, SV1
Janssen, PM1
Rafael-Fortney, JA1
Alcalay, RN1
Levy, OA1
Wolf, P1
Oliva, P1
Zhang, XK1
Waters, CH1
Fahn, S1
Kang, U1
Liong, C1
Ford, B1
Mazzoni, P1
Kuo, S1
Johnson, A1
Xiong, L1
Rouleau, GA1
Chung, W1
Marder, KS1
Gan-Or, Z1
Kamei, K1
Terao, T1
Katayama, Y1
Hatano, K1
Kodama, K1
Shirahama, M1
Sakai, A1
Hirakawa, H1
Mizokami, Y1
Shiotsuki, I1
Ishii, N1
Inoue, Y1
Akboga, MK1
Yayla, C1
Balci, KG1
Ozeke, O1
Maden, O1
Kisacik, H1
Temizhan, A1
Aydogdu, S1
Zhu, J2
Ying, SH1
Feng, MG1
Zhang, XG1
Li, H1
Wang, L1
Hao, YY1
Liang, GD1
Ma, YH1
Yang, GS1
Hu, JH1
Pfeifer, L1
Goertz, RS1
Neurath, MF1
Strobel, D1
Wildner, D1
Lin, JT1
Yang, XN1
Zhong, WZ1
Liao, RQ1
Dong, S1
Nie, Q1
Weng, SX1
Fang, XJ1
Zheng, JY1
Wu, YL1
Řezanka, T1
Kaineder, K1
Mezricky, D1
Řezanka, M1
Bišová, K1
Zachleder, V1
Vítová, M1
Rinker, JA1
Marshall, SA1
Mazzone, CM1
Lowery-Gionta, EG1
Gulati, V1
Pleil, KE1
Kash, TL1
Navarro, M1
Thiele, TE1
Zhang, Y1
Huang, Y1
Jin, Z1
Li, X1
Li, B1
Xu, P1
Huang, P1
Liu, C1
Fokdal, L1
Sturdza, A1
Mazeron, R1
Haie-Meder, C1
Tan, LT1
Gillham, C1
Šegedin, B1
Jürgenliemk-Schultz, I1
Kirisits, C1
Hoskin, P1
Pötter, R1
Lindegaard, JC1
Tanderup, K1
Levin, DE1
Schmitz, AJ1
Hines, SM1
Hines, KJ1
Tucker, MJ1
Brewer, SH1
Fenlon, EE1
Álvarez-Pérez, S1
Blanco, JL1
Peláez, T1
Martínez-Nevado, E1
García, ME1
Puckerin, AA1
Chang, DD1
Subramanyam, P1
Colecraft, HM1
Dogan, H1
Coteli, E1
Karatas, F1
Ceylan, O1
Sahin, MD1
Akdamar, G1
Kryczyk, A1
Żmudzki, P1
Hubicka, U1
Giovannelli, D1
Chung, M1
Staley, J1
Starovoytov, V1
Le Bris, N1
Vetriani, C1
Chen, W1
Wu, L1
Liu, X1
Shen, Y1
Liang, Y1
Tan, H1
Yang, Y1
Liu, Q1
Wang, M1
Liu, L1
Wang, X1
Liu, B1
Liu, GH1
Zhu, YJ1
Wang, JP1
Che, JM1
Chen, QQ1
Chen, Z1
Maucksch, U1
Runge, R1
Wunderlich, G1
Freudenberg, R1
Naumann, A1
Kotzerke, J1
Chen, JH1
Zheng, YL1
Xu, CQ1
Gu, LZ1
Ding, ZL1
Qin, L1
Wang, Y1
Fu, R1
Wan, YF1
Hu, CP1
Moody, TW1
Switzer, C1
Santana-Flores, W1
Ridnour, LA1
Berna, M1
Thill, M1
Jensen, RT1
Sparatore, A1
Del Soldato, P1
Yeh, GC1
Roberts, DD1
Giaccone, G1
Wink, DA1
Biran, A1
Brownstein, M1
Haklai, R1
Kloog, Y1
Chu, BF1
Karpenko, MJ1
Liu, Z1
Aimiuwu, J1
Villalona-Calero, MA1
Chan, KK1
Grever, MR1
Otterson, GA1
Singh, T1
Prasad, R1
Katiyar, SK1
Pratt, SE1
Durland-Busbice, S1
Shepard, RL1
Donoho, GP1
Starling, JJ1
Wickremsinhe, ER1
Perkins, EJ1
Dantzig, AH1
Ziauddin, MF1
Yeow, WS1
Maxhimer, JB1
Baras, A1
Chua, A1
Reddy, RM1
Tsai, W1
Cole, GW1
Schrump, DS1
Nguyen, DM1

Reviews

2 reviews available for valproic acid and Carcinoma, Non-Small Cell Lung

ArticleYear
Addressing the elephant in the room, therapeutic resistance in non-small cell lung cancer, with epigenetic therapies.
    Oncotarget, 2016, Jun-28, Volume: 7, Issue:26

    Topics: Antibodies, Monoclonal; Azacitidine; Azetidines; Benzamides; Biomarkers, Tumor; Carcinoma, Non-Small

2016
    Hand therapy, 2016, Volume: 21, Issue:1

    Topics: AC133 Antigen; Acenaphthenes; Acer; Acrosome Reaction; Adult; Agaricales; Aged; Aged, 80 and over; A

2016

Trials

1 trial available for valproic acid and Carcinoma, Non-Small Cell Lung

ArticleYear
Phase I study of 5-aza-2'-deoxycytidine in combination with valproic acid in non-small-cell lung cancer.
    Cancer chemotherapy and pharmacology, 2013, Volume: 71, Issue:1

    Topics: Adult; Aged; Antineoplastic Combined Chemotherapy Protocols; Azacitidine; Carcinoma, Non-Small-Cell

2013

Other Studies

12 other studies available for valproic acid and Carcinoma, Non-Small Cell Lung

ArticleYear
Tumors derived from lung cancer cells respond differently to treatment with sodium valproate (a HDAC inhibitor) in a chicken embryo chorioallantoic membrane model.
    Histology and histopathology, 2022, Volume: 37, Issue:12

    Topics: Animals; Carcinoma, Non-Small-Cell Lung; Cell Line, Tumor; Chick Embryo; Chickens; Chorioallantoic M

2022
Erlotinib-Valproic Acid Liquisolid Formulation: Evaluating Oral Bioavailability and Cytotoxicity in Erlotinib-Resistant Non-small Cell Lung Cancer Cells.
    AAPS PharmSciTech, 2019, Mar-04, Volume: 20, Issue:3

    Topics: Administration, Oral; Animals; Antineoplastic Agents; Biological Availability; Calcium Compounds; Ca

2019
Sodium valproate sensitizes non-small lung cancer A549 cells to γδ T-cell-mediated killing through upregulating the expression of MICA.
    Journal of biochemical and molecular toxicology, 2013, Volume: 27, Issue:11

    Topics: Carcinoma, Non-Small-Cell Lung; Cell Line, Tumor; Gene Expression Regulation, Neoplastic; Histocompa

2013
Potentiation of anticancer effect of valproic acid, an antiepileptic agent with histone deacetylase inhibitory activity, by the cyclin-dependent kinase inhibitor P276-00 in human non-small-cell lung cancer cell lines.
    Lung cancer (Amsterdam, Netherlands), 2013, Volume: 82, Issue:2

    Topics: Acetylation; Animals; Antineoplastic Agents; Apoptosis; Carcinoma, Non-Small-Cell Lung; Cell Cycle;

2013
Sodium valproate, a histone deacetylase inhibitor, enhances the efficacy of vinorelbine-cisplatin-based chemoradiation in non-small cell lung cancer cells.
    Anticancer research, 2014, Volume: 34, Issue:11

    Topics: Anticonvulsants; Antineoplastic Combined Chemotherapy Protocols; Apoptosis; Carcinoma, Non-Small-Cel

2014
Synergistic antitumor activity of histone deacetylase inhibitors and anti-ErbB3 antibody in NSCLC primary cultures via modulation of ErbB receptors expression.
    Oncotarget, 2016, Apr-12, Volume: 7, Issue:15

    Topics: Antibodies, Monoclonal; Carcinoma, Non-Small-Cell Lung; Cell Proliferation; Cell Survival; Drug Syne

2016
Valproic acid (VPA) enhances cisplatin sensitivity of non-small cell lung cancer cells via HDAC2 mediated down regulation of ABCA1.
    Biological chemistry, 2017, 06-27, Volume: 398, Issue:7

    Topics: Antineoplastic Agents; Apoptosis; ATP Binding Cassette Transporter 1; Carcinoma, Non-Small-Cell Lung

2017
Dithiolethione modified valproate and diclofenac increase E-cadherin expression and decrease proliferation of non-small cell lung cancer cells.
    Lung cancer (Amsterdam, Netherlands), 2010, Volume: 68, Issue:2

    Topics: Anethole Trithione; Animals; Cadherins; Carcinoma, Non-Small-Cell Lung; Cell Line, Tumor; Cell Proli

2010
Downregulation of survivin and aurora A by histone deacetylase and RAS inhibitors: a new drug combination for cancer therapy.
    International journal of cancer, 2011, Feb-01, Volume: 128, Issue:3

    Topics: Antineoplastic Agents; Antineoplastic Combined Chemotherapy Protocols; Aurora Kinases; Blotting, Wes

2011
Inhibition of class I histone deacetylases in non-small cell lung cancer by honokiol leads to suppression of cancer cell growth and induction of cell death in vitro and in vivo.
    Epigenetics, 2013, Volume: 8, Issue:1

    Topics: Acetylation; Animals; Biphenyl Compounds; Bronchi; Carcinoma, Non-Small-Cell Lung; Cell Death; Cell

2013
Efficacy of low-dose oral metronomic dosing of the prodrug of gemcitabine, LY2334737, in human tumor xenografts.
    Molecular cancer therapeutics, 2013, Volume: 12, Issue:4

    Topics: Administration, Metronomic; Administration, Oral; Animals; Carcinoma, Non-Small-Cell Lung; Cell Line

2013
Valproic acid, an antiepileptic drug with histone deacetylase inhibitory activity, potentiates the cytotoxic effect of Apo2L/TRAIL on cultured thoracic cancer cells through mitochondria-dependent caspase activation.
    Neoplasia (New York, N.Y.), 2006, Volume: 8, Issue:6

    Topics: Apoptosis; Apoptosis Regulatory Proteins; Carcinoma, Non-Small-Cell Lung; Caspases; Cell Line, Tumor

2006