Page last updated: 2024-10-26

valproic acid and Lung Neoplasms

valproic acid has been researched along with Lung Neoplasms in 31 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.

Lung Neoplasms: Tumors or cancer of the LUNG.

Research Excerpts

ExcerptRelevanceReference
"Gastrointestinal and pulmonary carcinoid cells were treated with either VPA or SBHA and lithium chloride for up to 48 hours."5.35Combination therapy with histone deacetylase inhibitors and lithium chloride: a novel treatment for carcinoid tumors. ( Adler, JT; Chen, H; Hottinger, DG; Kunnimalaiyaan, M, 2009)
" 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)
"Lung cancer is the most commonly diagnosed cancer worldwide with a high mortality rate."1.51Effective and new potent drug combination: Histone deacetylase and Wnt/β-catenin pathway inhibitors in lung carcinoma cells. ( Akgun, O; Ari, F; Erkisa, 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)
"Lung cancer is the leading cause of cancer mortality worldwide and despite efforts made to improve clinical results, continuing poor survival rates indicate that novel therapeutic approaches are needed."1.38Organosulfur derivatives of the HDAC inhibitor valproic acid sensitize human lung cancer cell lines to apoptosis and to cisplatin cytotoxicity. ( Amadori, D; Arienti, C; Brigliadori, G; Carloni, S; Del Soldato, P; Fabbri, F; Pasini, A; Silvestrini, R; Sparatore, A; Tesei, A; Ulivi, P; Zoli, W, 2012)
"Valproic acid (VPA), which is an effective antiepileptic drug, is known to inhibit the histone deacetylase activities."1.38Enhanced antitumor efficacy of telomerase-specific oncolytic adenovirus with valproic acid against human cancer cells. ( Fujiwara, T; Hashimoto, Y; Kagawa, S; Kawamura, H; Nagai, K; Tanaka, N; Urata, Y; Watanabe, Y, 2012)
" 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)
"Among the mechanisms of resistance of small cell lung carcinomas (SCLCs) to TRAIL is the lack of caspase-8 expression."1.37Combined inhibition of DNA methyltransferase and histone deacetylase restores caspase-8 expression and sensitizes SCLC cells to TRAIL. ( Kaminskyy, VO; Surova, OV; Vaculova, A; Zhivotovsky, B, 2011)
"Prognosis of small cell lung carcinoma (SCLC) is particularly poor, less than 5% of patients with extensive stage being alive after two years."1.36Preclinical evidence for a beneficial impact of valproate on the response of small cell lung cancer to first-line chemotherapy. ( Albelda, SM; Burny, A; Crisanti, C; Crisanti, MC; Hubaux, R; Kapoor, V; Mascaux, C; Vandermeers, F; Willems, L, 2010)
"Gastrointestinal and pulmonary carcinoid cells were treated with either VPA or SBHA and lithium chloride for up to 48 hours."1.35Combination therapy with histone deacetylase inhibitors and lithium chloride: a novel treatment for carcinoid tumors. ( Adler, JT; Chen, H; Hottinger, DG; Kunnimalaiyaan, M, 2009)
"Carcinoid tumors are neuroendocrine malignancies that frequently metastasize and secrete hormones that cause debilitating symptoms in patients."1.34Valproic acid activates notch-1 signaling and regulates the neuroendocrine phenotype in carcinoid cancer cells. ( Chen, H; Greenblatt, DY; Haymart, M; Jaskula-Sztul, R; Kunnimalaiyaan, M; Ning, L; Vaccaro, AM, 2007)

Research

Studies (31)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's6 (19.35)29.6817
2010's21 (67.74)24.3611
2020's4 (12.90)2.80

Authors

AuthorsStudies
Perrino, E1
Cappelletti, G1
Tazzari, V1
Giavini, E1
Del Soldato, P3
Sparatore, A3
Diržiuvienė, R1
Šlekienė, L1
Palubinskienė, J1
Balnytė, I1
Lasienė, K1
Stakišaitis, D1
Valančiūtė, A1
Chatziantoniou, A1
Zaravinos, A1
Guo, W1
Chen, Z2
Tan, L1
Wu, Q1
Ren, X1
Fu, C1
Du, Y1
Ren, J1
Meng, X1
Park, HK1
Han, BR1
Park, WH1
Bensaid, D1
Blondy, T1
Deshayes, S1
Dehame, V1
Bertrand, P1
Grégoire, M1
Errami, M1
Blanquart, C1
Patel, K1
Doddapaneni, R1
Patki, M1
Sekar, V1
Bagde, A1
Singh, M1
Akgun, O1
Erkisa, M1
Ari, F1
Shirsath, N1
Rathos, M1
Chaudhari, U1
Sivaramakrishnan, H1
Joshi, K1
Ding, S1
Pickard, AJ1
Kucera, GL1
Bierbach, U1
Gavrilov, V1
Lavrenkov, K1
Ariad, S1
Shany, S1
Noguchi, S1
Eitoku, M1
Moriya, S1
Kondo, S1
Kiyosawa, H1
Watanabe, T1
Suganuma, N1
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
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
Platta, CS1
Greenblatt, DY2
Kunnimalaiyaan, M3
Chen, H3
Adler, JT1
Hottinger, DG1
Moody, TW1
Switzer, C1
Santana-Flores, W1
Ridnour, LA1
Berna, M1
Thill, M1
Jensen, RT1
Yeh, GC1
Roberts, DD1
Giaccone, G1
Wink, DA1
Rui, J1
Long, D1
Wang, W1
Chou, T1
Zhang, ZG1
Li, XJ1
Fang, B1
Yuan, W1
Luo, Y1
Zhou, J1
Hubaux, R1
Vandermeers, F1
Crisanti, MC1
Crisanti, C1
Kapoor, V1
Burny, A1
Mascaux, C1
Albelda, SM1
Willems, L2
Biran, A1
Brownstein, M1
Haklai, R1
Kloog, Y1
Scherpereel, A1
Berghmans, T1
Lafitte, JJ1
Colinet, B1
Richez, M1
Bonduelle, Y1
Meert, AP1
Dhalluin, X1
Leclercq, N1
Paesmans, M1
Sculier, JP1
Kaminskyy, VO1
Surova, OV1
Vaculova, A1
Zhivotovsky, B1
Tesei, A1
Brigliadori, G1
Carloni, S1
Fabbri, F1
Ulivi, P1
Arienti, C1
Pasini, A1
Amadori, D1
Silvestrini, R1
Zoli, W1
Watanabe, Y1
Hashimoto, Y1
Kagawa, S1
Kawamura, H1
Nagai, K1
Tanaka, N1
Urata, Y1
Fujiwara, T1
Chu, BF1
Karpenko, MJ1
Liu, Z1
Aimiuwu, J1
Villalona-Calero, MA1
Chan, KK1
Grever, MR1
Otterson, GA1
Pratt, SE1
Durland-Busbice, S1
Shepard, RL1
Donoho, GP1
Starling, JJ1
Wickremsinhe, ER1
Perkins, EJ1
Dantzig, AH1
Gibbs, JP1
Adeyeye, MC1
Yang, Z1
Shen, DD1
Ziauddin, MF1
Yeow, WS1
Maxhimer, JB1
Baras, A1
Chua, A1
Reddy, RM1
Tsai, W1
Cole, GW1
Schrump, DS1
Nguyen, DM1
Vaccaro, AM1
Jaskula-Sztul, R1
Ning, L1
Haymart, M1

Clinical Trials (1)

Trial Overview

TrialPhaseEnrollmentStudy TypeStart DateStatus
A Phase II Study Assessing the Activity of Valproate Acid Plus Doxorubicin in Refractory or Recurrent Malignant Mesothelioma[NCT00634205]Phase 245 participants (Actual)Interventional2006-07-31Completed
[information is prepared from clinicaltrials.gov, extracted Sep-2024]

Reviews

2 reviews available for valproic acid and Lung Neoplasms

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

2 trials available for valproic acid and Lung Neoplasms

ArticleYear
Valproate-doxorubicin: promising therapy for progressing mesothelioma. A phase II study.
    The European respiratory journal, 2011, Volume: 37, Issue:1

    Topics: Aged; Aged, 80 and over; Antineoplastic Combined Chemotherapy Protocols; Disease Progression; Diseas

2011
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

27 other studies available for valproic acid and Lung Neoplasms

ArticleYear
New sulfurated derivatives of valproic acid with enhanced histone deacetylase inhibitory activity.
    Bioorganic & medicinal chemistry letters, 2008, Mar-15, Volume: 18, Issue:6

    Topics: Acetylation; Adenocarcinoma; Apoptosis; Blotting, Western; Cell Proliferation; Enzyme Inhibitors; Hi

2008
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
Signatures of Co-Deregulated Genes and Their Transcriptional Regulators in Lung Cancer.
    International journal of molecular sciences, 2022, Sep-18, Volume: 23, Issue:18

    Topics: Adenocarcinoma of Lung; Astemizole; Gene Expression Regulation, Neoplastic; Humans; Lung Neoplasms;

2022
l-Cysteine decorated nanoscale metal-organic frameworks delivering valproic acid/cisplatin for drug-resistant lung cancer therapy.
    Chemical communications (Cambridge, England), 2020, Apr-07, Volume: 56, Issue:27

    Topics: Animals; Antineoplastic Agents; Cell Line; Cell Survival; Cisplatin; Cysteine; Drug Delivery Systems

2020
Combination of Arsenic Trioxide and Valproic Acid Efficiently Inhibits Growth of Lung Cancer Cells via G2/M-Phase Arrest and Apoptotic Cell Death.
    International journal of molecular sciences, 2020, Apr-10, Volume: 21, Issue:7

    Topics: Animals; Antineoplastic Agents; Apoptosis; Arsenic Trioxide; Biomarkers; Cell Line, Tumor; Disease M

2020
Assessment of new HDAC inhibitors for immunotherapy of malignant pleural mesothelioma.
    Clinical epigenetics, 2018, Volume: 10

    Topics: B7-H1 Antigen; Benzamides; Cell Line, Tumor; Cell Proliferation; Cell Survival; Decitabine; DNA Meth

2018
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
Effective and new potent drug combination: Histone deacetylase and Wnt/β-catenin pathway inhibitors in lung carcinoma cells.
    Journal of cellular biochemistry, 2019, Volume: 120, Issue:9

    Topics: A549 Cells; Antineoplastic Combined Chemotherapy Protocols; Cell Line, Tumor; Cell Proliferation; Ce

2019
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
Design of enzymatically cleavable prodrugs of a potent platinum-containing anticancer agent.
    Chemistry (Weinheim an der Bergstrasse, Germany), 2014, Dec-01, Volume: 20, Issue:49

    Topics: Adenocarcinoma; Adenocarcinoma of Lung; Antineoplastic Agents; Cell Line, Tumor; Drug Design; Humans

2014
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
Regulation of Gene Expression by Sodium Valproate in Epithelial-to-Mesenchymal Transition.
    Lung, 2015, Volume: 193, Issue:5

    Topics: Acetylation; Antigens, CD; Cadherins; Cell Line, Tumor; Cell Survival; Collagen Type I; Collagen Typ

2015
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
Valproic acid induces Notch1 signaling in small cell lung cancer cells.
    The Journal of surgical research, 2008, Volume: 148, Issue:1

    Topics: Antineoplastic Agents; Basic Helix-Loop-Helix Transcription Factors; Biomarkers, Tumor; Blotting, We

2008
Combination therapy with histone deacetylase inhibitors and lithium chloride: a novel treatment for carcinoid tumors.
    Annals of surgical oncology, 2009, Volume: 16, Issue:2

    Topics: Adjuvants, Immunologic; Antineoplastic Combined Chemotherapy Protocols; Blotting, Western; Carcinoid

2009
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
[Valproic acid induce the expression of MICA antigen in human lung cancer cells and promote the NK killing effects on the cells].
    Sichuan da xue xue bao. Yi xue ban = Journal of Sichuan University. Medical science edition, 2010, Volume: 41, Issue:1

    Topics: Cell Line, Tumor; Cell Proliferation; Histocompatibility Antigens Class I; Humans; Killer Cells, Nat

2010
Preclinical evidence for a beneficial impact of valproate on the response of small cell lung cancer to first-line chemotherapy.
    European journal of cancer (Oxford, England : 1990), 2010, Volume: 46, Issue:9

    Topics: Animals; Antineoplastic Combined Chemotherapy Protocols; Apoptosis; Blotting, Western; Caspases; Cel

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
Combined inhibition of DNA methyltransferase and histone deacetylase restores caspase-8 expression and sensitizes SCLC cells to TRAIL.
    Carcinogenesis, 2011, Volume: 32, Issue:10

    Topics: Azacitidine; Blotting, Western; Caspase 8; Decitabine; DNA (Cytosine-5-)-Methyltransferase 1; DNA (C

2011
Organosulfur derivatives of the HDAC inhibitor valproic acid sensitize human lung cancer cell lines to apoptosis and to cisplatin cytotoxicity.
    Journal of cellular physiology, 2012, Volume: 227, Issue:10

    Topics: Apoptosis; Cell Line, Tumor; Cisplatin; Drug Synergism; Histone Deacetylase 1; Histone Deacetylase I

2012
Enhanced antitumor efficacy of telomerase-specific oncolytic adenovirus with valproic acid against human cancer cells.
    Cancer gene therapy, 2012, Volume: 19, Issue:11

    Topics: Adenoviridae; Adenovirus E1A Proteins; Adenovirus E1B Proteins; Antineoplastic Agents; Cell Line, Tu

2012
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 uptake by bovine brain microvessel endothelial cells: role of active efflux transport.
    Epilepsy research, 2004, Volume: 58, Issue:1

    Topics: Adenocarcinoma; Animals; Biological Transport, Active; Brain; Cattle; Cells, Cultured; Cyclooxygenas

2004
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
Valproic acid activates notch-1 signaling and regulates the neuroendocrine phenotype in carcinoid cancer cells.
    The oncologist, 2007, Volume: 12, Issue:8

    Topics: Animals; Antineoplastic Agents; Carcinoid Tumor; Cell Cycle; Cell Line, Tumor; Cell Proliferation; C

2007