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Volumn 331, Issue , 2015, Pages 112-118

Histone deacetylase inhibitor attenuates neurotoxicity of clioquinol in PC12 cells

Author keywords

Clioquinol; Deacetylation of histones; Histone deacetylase inhibitor; Subacute myeloopticoneuropathy

Indexed keywords

CLIOQUINOL; HISTONE; NERVE GROWTH FACTOR; TRICHOSTATIN A; HISTONE DEACETYLASE INHIBITOR; HYDROXAMIC ACID; NEUROPROTECTIVE AGENT; PROTEIN TYROSINE KINASE A;

EID: 84925310885     PISSN: 0300483X     EISSN: 18793185     Source Type: Journal    
DOI: 10.1016/j.tox.2015.01.013     Document Type: Article
Times cited : (13)

References (34)
  • 1
    • 71849099656 scopus 로고    scopus 로고
    • Clioquinol inhibits NGF-induced Trk autophosphorylation and neurite outgrowth in PC12 cells
    • Asakura K., Ueda A., Kawamura N., Ueda M., Mihara T., Mutoh T. Clioquinol inhibits NGF-induced Trk autophosphorylation and neurite outgrowth in PC12 cells. Brain Res. 2009, 1301:110-115.
    • (2009) Brain Res. , vol.1301 , pp. 110-115
    • Asakura, K.1    Ueda, A.2    Kawamura, N.3    Ueda, M.4    Mihara, T.5    Mutoh, T.6
  • 5
    • 33847746963 scopus 로고    scopus 로고
    • Clioquinol a therapeutic agent for Alzheimer's disease, has proteasome-inhibitory, androgen receptor-suppressing, apoptosis-inducing, and antitumor activities in human prostate cancer cells and xenografts
    • Chen D., Cui Q.C., Yang H., Barrea R.A., Sarkar F.H., Sheng S., Yan B., Reddy G.P., Dou Q.P. Clioquinol a therapeutic agent for Alzheimer's disease, has proteasome-inhibitory, androgen receptor-suppressing, apoptosis-inducing, and antitumor activities in human prostate cancer cells and xenografts. Cancer Res. 2007, 67:1636-1644.
    • (2007) Cancer Res. , vol.67 , pp. 1636-1644
    • Chen, D.1    Cui, Q.C.2    Yang, H.3    Barrea, R.A.4    Sarkar, F.H.5    Sheng, S.6    Yan, B.7    Reddy, G.P.8    Dou, Q.P.9
  • 6
    • 0034964390 scopus 로고    scopus 로고
    • Treatment with a copper-zinc chelator markedly and rapidly inhibits beta-amyloid accumulation in Alzheimer's disease transgenic mice
    • Cherny R.A., Atwood C.S., Xilinas M.E., Gray D.N., Jones W.D., McLean C.A., Barnham K.J. Treatment with a copper-zinc chelator markedly and rapidly inhibits beta-amyloid accumulation in Alzheimer's disease transgenic mice. Neuron 2001, 30:665-676.
    • (2001) Neuron , vol.30 , pp. 665-676
    • Cherny, R.A.1    Atwood, C.S.2    Xilinas, M.E.3    Gray, D.N.4    Jones, W.D.5    McLean, C.A.6    Barnham, K.J.7
  • 7
    • 77952875979 scopus 로고    scopus 로고
    • HDAC inhibitors and neurodegeneration: at the edge between protection and damage
    • Dietz K.C., Casaccia P. HDAC inhibitors and neurodegeneration: at the edge between protection and damage. Pharmacol. Res. 2010, 62:11-17.
    • (2010) Pharmacol. Res. , vol.62 , pp. 11-17
    • Dietz, K.C.1    Casaccia, P.2
  • 10
    • 84872601036 scopus 로고    scopus 로고
    • Histone acetylation: molecular mnemonics on the chromatin
    • Gräff J., Tsai L.H. Histone acetylation: molecular mnemonics on the chromatin. Nat. Rev. Neurosci. 2013, 14:97-111.
    • (2013) Nat. Rev. Neurosci. , vol.14 , pp. 97-111
    • Gräff, J.1    Tsai, L.H.2
  • 11
    • 57749170458 scopus 로고    scopus 로고
    • The many roles of histone deacetylases in development and physiology: implications for disease and therapy
    • Haberland M., Montgomery R.L., Olson E.N. The many roles of histone deacetylases in development and physiology: implications for disease and therapy. Nat. Rev. Genet. 2009, 10:32-42.
    • (2009) Nat. Rev. Genet. , vol.10 , pp. 32-42
    • Haberland, M.1    Montgomery, R.L.2    Olson, E.N.3
  • 12
    • 84862307896 scopus 로고    scopus 로고
    • Clioquinol induces DNA double-strand breaks, activation of ATM, and subsequent activation of p53 signaling
    • Katsuyama M., Iwata K., Ibi M., Matsuno K., Matsumoto M., Yabe-Nishimura C. Clioquinol induces DNA double-strand breaks, activation of ATM, and subsequent activation of p53 signaling. Toxicology 2012, 299:55-59.
    • (2012) Toxicology , vol.299 , pp. 55-59
    • Katsuyama, M.1    Iwata, K.2    Ibi, M.3    Matsuno, K.4    Matsumoto, M.5    Yabe-Nishimura, C.6
  • 17
    • 84862965909 scopus 로고    scopus 로고
    • Histone deacetylase inhibitors prevent the degradation and restore the activity of glucocerebrosidase in Gaucher disease
    • Lu J., Yang C., Chen M., Ye D.Y., Lonser R.R., Brady R.O., Zhuang Z. Histone deacetylase inhibitors prevent the degradation and restore the activity of glucocerebrosidase in Gaucher disease. Proc. Natl. Acad. Sci. U. S. A. 2011, 108:21200-21205.
    • (2011) Proc. Natl. Acad. Sci. U. S. A. , vol.108 , pp. 21200-21205
    • Lu, J.1    Yang, C.2    Chen, M.3    Ye, D.Y.4    Lonser, R.R.5    Brady, R.O.6    Zhuang, Z.7
  • 18
    • 84879531836 scopus 로고    scopus 로고
    • Histone deacetylase inhibitors are neuroprotective and preserve NGF-mediated cell survival following traumatic brain injury
    • Lu J., Frerich J.M., Turtzo L.C., et al. Histone deacetylase inhibitors are neuroprotective and preserve NGF-mediated cell survival following traumatic brain injury. Proc. Nat. Acad. Sci. U. S. A. 2013, 110:10747-10752.
    • (2013) Proc. Nat. Acad. Sci. U. S. A. , vol.110 , pp. 10747-10752
    • Lu, J.1    Frerich, J.M.2    Turtzo, L.C.3
  • 19
    • 0031457107 scopus 로고    scopus 로고
    • SMON and pharmacokinetics of chinoform with special reference to animal species difference
    • [in Japanese with English abstract]
    • Matsuki Y., Yoshimura S., Abe M. SMON and pharmacokinetics of chinoform with special reference to animal species difference. Yakugaku Zasshi 1997, 7:936-956. [in Japanese with English abstract].
    • (1997) Yakugaku Zasshi , vol.7 , pp. 936-956
    • Matsuki, Y.1    Yoshimura, S.2    Abe, M.3
  • 20
    • 30344477367 scopus 로고    scopus 로고
    • Histone deacetylase inhibitors and the promise of epigenetic (and more) treatments for cancer
    • Minucci S., Pelicci P.G. Histone deacetylase inhibitors and the promise of epigenetic (and more) treatments for cancer. Nat. Rev. Cancer 2006, 6:38-51.
    • (2006) Nat. Rev. Cancer , vol.6 , pp. 38-51
    • Minucci, S.1    Pelicci, P.G.2
  • 21
    • 0034530123 scopus 로고    scopus 로고
    • Unglycosylated Trk protein does not co-localize nor associate with ganglioside GM1 in stable clone of PC12 cells overexpressing Trk (PCtrk cells)
    • Mutoh T., Hamano T., Tokuda A., Kuriyama M. Unglycosylated Trk protein does not co-localize nor associate with ganglioside GM1 in stable clone of PC12 cells overexpressing Trk (PCtrk cells). Glycoconj. J. 2000, 17:233-237.
    • (2000) Glycoconj. J. , vol.17 , pp. 233-237
    • Mutoh, T.1    Hamano, T.2    Tokuda, A.3    Kuriyama, M.4
  • 23
    • 0015937048 scopus 로고
    • Relation between subacute myelo-optic neuropathy (S.M.O.N.) and clioquinol: nationwide survey
    • Nakae K., Yamamoto S., Shigematsu I., Kono R. Relation between subacute myelo-optic neuropathy (S.M.O.N.) and clioquinol: nationwide survey. Lancet 1973, 1:171-173.
    • (1973) Lancet , vol.1 , pp. 171-173
    • Nakae, K.1    Yamamoto, S.2    Shigematsu, I.3    Kono, R.4
  • 24
    • 23844482456 scopus 로고    scopus 로고
    • Clioquinol down-regulates mutant huntingtin expression in vitro and mitigates pathology in a Huntington's disease mouse model
    • Nguyen T., Hamby A., Massa S.M. Clioquinol down-regulates mutant huntingtin expression in vitro and mitigates pathology in a Huntington's disease mouse model. Proc. Natl. Acad. Sci. U. S. A. 2005, 102:11840-11856.
    • (2005) Proc. Natl. Acad. Sci. U. S. A. , vol.102 , pp. 11840-11856
    • Nguyen, T.1    Hamby, A.2    Massa, S.M.3
  • 25
    • 10744224267 scopus 로고    scopus 로고
    • Metal-protein attenuation with iodochlorhydroxyquin (clioquinol) targeting Abeta amyloid deposition and toxicity in Alzheimer disease: a pilot phase 2 clinical trial
    • Ritchie C.W., Bush A.I., Mackinnon A., Macfarlane S., Mastwyk M., MacGregor L., et al. Metal-protein attenuation with iodochlorhydroxyquin (clioquinol) targeting Abeta amyloid deposition and toxicity in Alzheimer disease: a pilot phase 2 clinical trial. Arch. Neurol. 2003, 60:1685-1691.
    • (2003) Arch. Neurol. , vol.60 , pp. 1685-1691
    • Ritchie, C.W.1    Bush, A.I.2    Mackinnon, A.3    Macfarlane, S.4    Mastwyk, M.5    MacGregor, L.6
  • 26
    • 0000279236 scopus 로고
    • Neuropathological aspects of the etiopathogenesis of subacute myelo-optico-neuropathy (SMON)
    • North-Holland, Amsterdam
    • Shiraki H., et al. Neuropathological aspects of the etiopathogenesis of subacute myelo-optico-neuropathy (SMON). Intoxications of the Nervous System: Part 2. Handbook of Clinical Neurology 1979, vol. 37:141-198. North-Holland, Amsterdam.
    • (1979) Intoxications of the Nervous System: Part 2. Handbook of Clinical Neurology , vol.37 , pp. 141-198
    • Shiraki, H.1
  • 28
    • 84868549261 scopus 로고    scopus 로고
    • Mercaptoacetamide-based class II HDAC inhibitor lowers Abeta levels and improves learning and memory in a mouse model of Alzheimer's disease
    • Sung Y.M., Lee T., Yoon H., et al. Mercaptoacetamide-based class II HDAC inhibitor lowers Abeta levels and improves learning and memory in a mouse model of Alzheimer's disease. Exp. Neurol. 2013, 239:192-201.
    • (2013) Exp. Neurol. , vol.239 , pp. 192-201
    • Sung, Y.M.1    Lee, T.2    Yoon, H.3
  • 29
    • 0033781375 scopus 로고    scopus 로고
    • Subacute myelo-optico-neuropathy: clioquinol intoxication in humans and animals
    • Tateishi J. Subacute myelo-optico-neuropathy: clioquinol intoxication in humans and animals. Neuropathology 2000, (Suppl. 20):S20-S24.
    • (2000) Neuropathology , pp. S20-S24
    • Tateishi, J.1
  • 30
    • 0015208991 scopus 로고
    • Neurological syndrome associated with clioquinol
    • Tsubaki T., Honma Y., Hoshi M. Neurological syndrome associated with clioquinol. Lancet 1971, 1:696-697.
    • (1971) Lancet , vol.1 , pp. 696-697
    • Tsubaki, T.1    Honma, Y.2    Hoshi, M.3
  • 31
    • 84922437992 scopus 로고    scopus 로고
    • Inhibitors of histone deacetylases enhance neurotoxicity of DNA damage
    • Vashishta A., Hetman M. Inhibitors of histone deacetylases enhance neurotoxicity of DNA damage. Neuromol. Med. 2014, 16:727-741.
    • (2014) Neuromol. Med. , vol.16 , pp. 727-741
    • Vashishta, A.1    Hetman, M.2
  • 32
    • 80054736157 scopus 로고    scopus 로고
    • Potential non-oncological applications of histone deacetylase inhibitors
    • Ververis K., Karagiannis T.C. Potential non-oncological applications of histone deacetylase inhibitors. Am. J. Transl. Res. 2011, 3:454-467.
    • (2011) Am. J. Transl. Res. , vol.3 , pp. 454-467
    • Ververis, K.1    Karagiannis, T.C.2
  • 33
    • 50249083844 scopus 로고    scopus 로고
    • Histone deacetylases as transducers and targets of nuclear signaling
    • Walkinshaw D.R., Tahmasebi S., Bertos N.R., Yang X.J. Histone deacetylases as transducers and targets of nuclear signaling. J. Cell. Biochem. 2008, 104:1541-1552.
    • (2008) J. Cell. Biochem. , vol.104 , pp. 1541-1552
    • Walkinshaw, D.R.1    Tahmasebi, S.2    Bertos, N.R.3    Yang, X.J.4
  • 34
    • 84896038598 scopus 로고    scopus 로고
    • Histone decacetylase inhibitors prevent mitochondrial fragmentation and elicit early neuroprotection against MPP+
    • Zhu M., Li W.W., Lu C.Z. Histone decacetylase inhibitors prevent mitochondrial fragmentation and elicit early neuroprotection against MPP+. CNS Neurosci. Ther. 2014, 20:308-316.
    • (2014) CNS Neurosci. Ther. , vol.20 , pp. 308-316
    • Zhu, M.1    Li, W.W.2    Lu, C.Z.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.