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4-phenylbutyric acid and Glioblastoma

4-phenylbutyric acid has been researched along with Glioblastoma in 7 studies

4-phenylbutyric acid: RN refers to the parent cpd
4-phenylbutyric acid : A monocarboxylic acid the structure of which is that of butyric acid substituted with a phenyl group at C-4. It is a histone deacetylase inhibitor that displays anticancer activity. It inhibits cell proliferation, invasion and migration and induces apoptosis in glioma cells. It also inhibits protein isoprenylation, depletes plasma glutamine, increases production of foetal haemoglobin through transcriptional activation of the gamma-globin gene and affects hPPARgamma activation.

Glioblastoma: A malignant form of astrocytoma histologically characterized by pleomorphism of cells, nuclear atypia, microhemorrhage, and necrosis. They may arise in any region of the central nervous system, with a predilection for the cerebral hemispheres, basal ganglia, and commissural pathways. Clinical presentation most frequently occurs in the fifth or sixth decade of life with focal neurologic signs or seizures.

Research Excerpts

ExcerptRelevanceReference
" In this study we show that the chemical chaperone, glycerol, and the transcriptional regulator, sodium 4-phenylbutyrate, inhibit the constitutively activated inward current and reduce cell growth and migration in glioblastoma multiforme."7.73Surface expression of ASIC2 inhibits the amiloride-sensitive current and migration of glioma cells. ( Benos, DJ; Bubien, JK; Colby, G; Esimai, O; Fuller, CM; Gillespie, GY; Jovov, B; Kovacs, GG; Mapstone, TB; Markert, JM; Pahwa, AK; Vila-Carriles, WH; Zhou, ZH, 2006)
"We have investigated in vitro effects of anticancer therapy with the histone deacetylase inhibitor (HDACi) 4-phenylbutyrate (4-PB) combined with receptor tyrosine kinase inhibitors (RTKi) gefitinib or vandetanib on the survival of glioblastoma (U343MGa) and medulloblastoma (D324Med) cells."3.77Enhanced effects by 4-phenylbutyrate in combination with RTK inhibitors on proliferation in brain tumor cell models. ( Baryawno, N; Ekström, TJ; Johnsen, JI; Larsson, C; Marino, AM; Sofiadis, A; Vukojević, V, 2011)
" In this study we show that the chemical chaperone, glycerol, and the transcriptional regulator, sodium 4-phenylbutyrate, inhibit the constitutively activated inward current and reduce cell growth and migration in glioblastoma multiforme."3.73Surface expression of ASIC2 inhibits the amiloride-sensitive current and migration of glioma cells. ( Benos, DJ; Bubien, JK; Colby, G; Esimai, O; Fuller, CM; Gillespie, GY; Jovov, B; Kovacs, GG; Mapstone, TB; Markert, JM; Pahwa, AK; Vila-Carriles, WH; Zhou, ZH, 2006)

Research

Studies (7)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (14.29)18.2507
2000's4 (57.14)29.6817
2010's1 (14.29)24.3611
2020's1 (14.29)2.80

Authors

AuthorsStudies
Romeo, MA1
Gilardini Montani, MS1
Benedetti, R1
Garufi, A1
D'Orazi, G1
Cirone, M1
Marino, AM1
Sofiadis, A1
Baryawno, N1
Johnsen, JI1
Larsson, C1
Vukojević, V1
Ekström, TJ3
Asklund, T1
Appelskog, IB2
Ammerpohl, O2
Almqvist, PM2
Svechnikova, IG1
Lui, WO1
Vila-Carriles, WH1
Kovacs, GG1
Jovov, B1
Zhou, ZH1
Pahwa, AK1
Colby, G1
Esimai, O1
Gillespie, GY1
Mapstone, TB1
Markert, JM1
Fuller, CM1
Bubien, JK1
Benos, DJ1
Lopez, CA1
Feng, FY1
Herman, JM1
Nyati, MK1
Lawrence, TS1
Ljungman, M1
Engelhard, HH1
Homer, RJ1
Duncan, HA1
Rozental, J1

Other Studies

7 other studies available for 4-phenylbutyric acid and Glioblastoma

ArticleYear
PBA Preferentially Impairs Cell Survival of Glioblastomas Carrying mutp53 by Reducing Its Expression Level, Stabilizing wtp53, Downregulating the Mevalonate Kinase and Dysregulating UPR.
    Biomolecules, 2020, 04-10, Volume: 10, Issue:4

    Topics: Brain Neoplasms; Butyric Acid; Cell Line, Tumor; Cell Survival; Down-Regulation; Glioblastoma; Human

2020
Enhanced effects by 4-phenylbutyrate in combination with RTK inhibitors on proliferation in brain tumor cell models.
    Biochemical and biophysical research communications, 2011, Jul-22, Volume: 411, Issue:1

    Topics: Antineoplastic Combined Chemotherapy Protocols; Brain Neoplasms; Cell Line, Tumor; Cell Proliferatio

2011
Histone deacetylase inhibitor 4-phenylbutyrate modulates glial fibrillary acidic protein and connexin 43 expression, and enhances gap-junction communication, in human glioblastoma cells.
    European journal of cancer (Oxford, England : 1990), 2004, Volume: 40, Issue:7

    Topics: Antineoplastic Agents; Blotting, Western; Cell Communication; Connexin 43; Gap Junctions; Glial Fibr

2004
Histone deacetylase inhibitor 4-phenylbutyrate suppresses GAPDH mRNA expression in glioma cells.
    International journal of oncology, 2004, Volume: 24, Issue:6

    Topics: Animals; Antineoplastic Agents; Apoptosis; Brain Neoplasms; Cell Division; Down-Regulation; Enzyme I

2004
Surface expression of ASIC2 inhibits the amiloride-sensitive current and migration of glioma cells.
    The Journal of biological chemistry, 2006, Jul-14, Volume: 281, Issue:28

    Topics: Acid Sensing Ion Channels; Amiloride; Antineoplastic Agents; Brain Neoplasms; Cell Membrane; Cell Mo

2006
Phenylbutyrate sensitizes human glioblastoma cells lacking wild-type p53 function to ionizing radiation.
    International journal of radiation oncology, biology, physics, 2007, Sep-01, Volume: 69, Issue:1

    Topics: Acetylation; Cell Line, Tumor; Cell Proliferation; G1 Phase; Glioblastoma; Histone Deacetylase Inhib

2007
Inhibitory effects of phenylbutyrate on the proliferation, morphology, migration and invasiveness of malignant glioma cells.
    Journal of neuro-oncology, 1998, Volume: 37, Issue:2

    Topics: Apoptosis; Cell Cycle; Cell Division; Cell Movement; Glioblastoma; Humans; Neoplasm Invasiveness; Ph

1998