Page last updated: 2024-11-04

rolipram and Brain Neoplasms

rolipram has been researched along with Brain Neoplasms in 6 studies

Brain Neoplasms: Neoplasms of the intracranial components of the central nervous system, including the cerebral hemispheres, basal ganglia, hypothalamus, thalamus, brain stem, and cerebellum. Brain neoplasms are subdivided into primary (originating from brain tissue) and secondary (i.e., metastatic) forms. Primary neoplasms are subdivided into benign and malignant forms. In general, brain tumors may also be classified by age of onset, histologic type, or presenting location in the brain.

Research Excerpts

ExcerptRelevanceReference
"Bradykinin causes a concentration-dependent, transient rise in intracellular Ca2+ and a sustained inhibition of forskolin-, dopamine- and 5'-N-ethyl-carboxamidoadenosine (NECA)-stimulated cAMP accumulation in D384 astrocytoma cells."7.68Bradykinin inhibits cyclic AMP accumulation in D384-human astrocytoma cells via a calcium-dependent inhibition of adenylyl cyclase. ( Altiok, N; Fredholm, BB, 1993)
"Bradykinin causes a concentration-dependent, transient rise in intracellular Ca2+ and a sustained inhibition of forskolin-, dopamine- and 5'-N-ethyl-carboxamidoadenosine (NECA)-stimulated cAMP accumulation in D384 astrocytoma cells."3.68Bradykinin inhibits cyclic AMP accumulation in D384-human astrocytoma cells via a calcium-dependent inhibition of adenylyl cyclase. ( Altiok, N; Fredholm, BB, 1993)
"Rolipram-treated A172 or U87MG cell survival was lower in the presence of forskolin, adenylate cyclase activator, than that in its absence."1.38Phosphodiesterase inhibitors control A172 human glioblastoma cell death through cAMP-mediated activation of protein kinase A and Epac1/Rap1 pathways. ( Kim, HM; Lee, GH; Lee, JW; Lee, MS; Moon, EY, 2012)
"As favorable outcomes from malignant brain tumors remain limited by poor survival and treatment-related toxicity, novel approaches to cure are essential."1.35Targeted inhibition of cyclic AMP phosphodiesterase-4 promotes brain tumor regression. ( Goldhoff, P; Hope, A; Jackson, E; Limbrick, DD; Perry, A; Piwnica-Worms, D; Rubin, JB; Warrington, NM; Woerner, BM, 2008)

Research

Studies (6)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (16.67)18.2507
2000's3 (50.00)29.6817
2010's2 (33.33)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Ramezani, S1
Vousooghi, N1
Ramezani Kapourchali, F1
Yousefzadeh-Chabok, S1
Reihanian, Z1
Alizadeh, AM1
Khodayari, S1
Khodayari, H1
Goldhoff, P1
Warrington, NM1
Limbrick, DD1
Hope, A1
Woerner, BM2
Jackson, E2
Perry, A2
Piwnica-Worms, D2
Rubin, JB2
Schmidt, AL1
de Farias, CB1
Abujamra, AL1
Brunetto, AL1
Schwartsmann, G1
Roesler, R1
Moon, EY1
Lee, GH1
Lee, MS1
Kim, HM1
Lee, JW1
Yang, L1
Altiok, N1
Fredholm, BB1

Other Studies

6 other studies available for rolipram and Brain Neoplasms

ArticleYear
Rolipram optimizes therapeutic effect of bevacizumab by enhancing proapoptotic, antiproliferative signals in a glioblastoma heterotopic model.
    Life sciences, 2019, Dec-15, Volume: 239

    Topics: Angiogenesis Inhibitors; Animals; Antineoplastic Combined Chemotherapy Protocols; Apoptosis; Bevaciz

2019
Targeted inhibition of cyclic AMP phosphodiesterase-4 promotes brain tumor regression.
    Clinical cancer research : an official journal of the American Association for Cancer Research, 2008, Dec-01, Volume: 14, Issue:23

    Topics: Adolescent; Adult; Aged; Animals; Antineoplastic Agents; Blotting, Western; Brain Neoplasms; Cell Li

2008
Phosphodiesterase-4 inhibition and brain tumor growth.
    Clinical cancer research : an official journal of the American Association for Cancer Research, 2009, May-01, Volume: 15, Issue:9

    Topics: Animals; Brain Neoplasms; Cerebellar Neoplasms; Cyclic Nucleotide Phosphodiesterases, Type 4; Medull

2009
Phosphodiesterase inhibitors control A172 human glioblastoma cell death through cAMP-mediated activation of protein kinase A and Epac1/Rap1 pathways.
    Life sciences, 2012, Feb-27, Volume: 90, Issue:9-10

    Topics: 1-Methyl-3-isobutylxanthine; Antineoplastic Combined Chemotherapy Protocols; Apoptosis; Brain Neopla

2012
Blocking CXCR4-mediated cyclic AMP suppression inhibits brain tumor growth in vivo.
    Cancer research, 2007, Jan-15, Volume: 67, Issue:2

    Topics: Animals; Brain Neoplasms; Cell Growth Processes; Cell Line, Tumor; Chemokine CXCL12; Chemokines, CXC

2007
Bradykinin inhibits cyclic AMP accumulation in D384-human astrocytoma cells via a calcium-dependent inhibition of adenylyl cyclase.
    Cellular signalling, 1993, Volume: 5, Issue:3

    Topics: 1-Methyl-3-isobutylxanthine; Adenosine; Adenosine-5'-(N-ethylcarboxamide); Adenylyl Cyclase Inhibito

1993