SIRT2- and NRF2-Targeting Thiazole-Containing Compound with Therapeutic Activity in Huntington's Disease Models

Luisa Quinti; Malcolm Casale; Sébastien Moniot; Teresa F. Pais; Michael J. Van Kanegan; Linda S. Kaltenbach; Judit Pallos; Ryan G. Lim; Sharadha Dayalan Naidu; Heike Runne; Lisa Meisel; Nazifa Abdul Rauf; Dmitriy Leyfer; Michele M. Maxwell; Eddine Saiah; John E. Landers; Ruth Luthi-Carter; Ruben Abagyan; Albena T. Dinkova-Kostova; Clemens Steegborn; J. Lawrence Marsh; Donald C. Lo; Leslie M. Thompson; Aleksey G. Kazantsev

doi:10.1016/j.chembiol.2016.05.015

SIRT2- and NRF2-Targeting Thiazole-Containing Compound with Therapeutic Activity in Huntington's Disease Models

Luisa Quinti
, Malcolm Casale
, Sébastien Moniot
, Teresa F. Pais
, Michael J. Van Kanegan
, Linda S. Kaltenbach
, Judit Pallos
, Ryan G. Lim
, Sharadha Dayalan Naidu
, Heike Runne
, Lisa Meisel
, Nazifa Abdul Rauf
, Dmitriy Leyfer
, Michele M. Maxwell
, Eddine Saiah
, John E. Landers
, Ruth Luthi-Carter
, Ruben Abagyan
, Albena T. Dinkova-Kostova
, Clemens Steegborn

J. Lawrence Marsh, Donald C. Lo, Leslie M. Thompson, Aleksey G. Kazantsev

Resultado de pesquisa: ???type-name??? › ???researchoutput.researchoutputtypes.contributiontojournal.article??? › revisão de pares

81 Citações (Scopus)

Resumo

There are currently no disease-modifying therapies for the neurodegenerative disorder Huntington's disease (HD). This study identified novel thiazole-containing inhibitors of the deacetylase sirtuin-2 (SIRT2) with neuroprotective activity in ex vivo brain slice and Drosophila models of HD. A systems biology approach revealed an additional SIRT2-independent property of the lead-compound, MIND4, as an inducer of cytoprotective NRF2 (nuclear factor-erythroid 2 p45-derived factor 2) activity. Structure-activity relationship studies further identified a potent NRF2 activator (MIND4-17) lacking SIRT2 inhibitory activity. MIND compounds induced NRF2 activation responses in neuronal and non-neuronal cells and reduced production of reactive oxygen species and nitrogen intermediates. These drug-like thiazole-containing compounds represent an exciting opportunity for development of multi-targeted agents with potentially synergistic therapeutic benefits in HD and related disorders.

Idioma original	???core.languages.en_GB???
Páginas (de-até)	849-861
Número de páginas	13
Revista	Cell Chemical Biology
Volume	23
Número de emissão	7
DOIs	https://doi.org/10.1016/j.chembiol.2016.05.015
Estado da publicação	???researchoutput.status.published??? - 21 jul. 2016
Publicado externamente	Sim

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Quinti, L., Casale, M., Moniot, S., Pais, T. F., Van Kanegan, M. J., Kaltenbach, L. S., Pallos, J., Lim, R. G., Naidu, S. D., Runne, H., Meisel, L., Rauf, N. A., Leyfer, D., Maxwell, M. M., Saiah, E., Landers, J. E., Luthi-Carter, R., Abagyan, R., Dinkova-Kostova, A. T., ... Kazantsev, A. G. (2016). SIRT2- and NRF2-Targeting Thiazole-Containing Compound with Therapeutic Activity in Huntington's Disease Models. Cell Chemical Biology, 23(7), 849-861. https://doi.org/10.1016/j.chembiol.2016.05.015

@article{10b46084a5dc4cc39973462e9753fbdc,

title = "SIRT2- and NRF2-Targeting Thiazole-Containing Compound with Therapeutic Activity in Huntington's Disease Models",

abstract = "There are currently no disease-modifying therapies for the neurodegenerative disorder Huntington's disease (HD). This study identified novel thiazole-containing inhibitors of the deacetylase sirtuin-2 (SIRT2) with neuroprotective activity in ex vivo brain slice and Drosophila models of HD. A systems biology approach revealed an additional SIRT2-independent property of the lead-compound, MIND4, as an inducer of cytoprotective NRF2 (nuclear factor-erythroid 2 p45-derived factor 2) activity. Structure-activity relationship studies further identified a potent NRF2 activator (MIND4-17) lacking SIRT2 inhibitory activity. MIND compounds induced NRF2 activation responses in neuronal and non-neuronal cells and reduced production of reactive oxygen species and nitrogen intermediates. These drug-like thiazole-containing compounds represent an exciting opportunity for development of multi-targeted agents with potentially synergistic therapeutic benefits in HD and related disorders.",

author = "Luisa Quinti and Malcolm Casale and S{\'e}bastien Moniot and Pais, \{Teresa F.\} and \{Van Kanegan\}, \{Michael J.\} and Kaltenbach, \{Linda S.\} and Judit Pallos and Lim, \{Ryan G.\} and Naidu, \{Sharadha Dayalan\} and Heike Runne and Lisa Meisel and Rauf, \{Nazifa Abdul\} and Dmitriy Leyfer and Maxwell, \{Michele M.\} and Eddine Saiah and Landers, \{John E.\} and Ruth Luthi-Carter and Ruben Abagyan and Dinkova-Kostova, \{Albena T.\} and Clemens Steegborn and Marsh, \{J. Lawrence\} and Lo, \{Donald C.\} and Thompson, \{Leslie M.\} and Kazantsev, \{Aleksey G.\}",

note = "Publisher Copyright: {\textcopyright} 2016 Elsevier Ltd",

year = "2016",

month = jul,

day = "21",

doi = "10.1016/j.chembiol.2016.05.015",

language = "English",

volume = "23",

pages = "849--861",

journal = "Cell Chemical Biology",

issn = "2451-9456",

publisher = "Elsevier Ltd.",

number = "7",

}

Quinti, L, Casale, M, Moniot, S, Pais, TF, Van Kanegan, MJ, Kaltenbach, LS, Pallos, J, Lim, RG, Naidu, SD, Runne, H, Meisel, L, Rauf, NA, Leyfer, D, Maxwell, MM, Saiah, E, Landers, JE, Luthi-Carter, R, Abagyan, R, Dinkova-Kostova, AT, Steegborn, C, Marsh, JL, Lo, DC, Thompson, LM & Kazantsev, AG 2016, 'SIRT2- and NRF2-Targeting Thiazole-Containing Compound with Therapeutic Activity in Huntington's Disease Models', Cell Chemical Biology, vol. 23, n.º 7, pp. 849-861. https://doi.org/10.1016/j.chembiol.2016.05.015

SIRT2- and NRF2-Targeting Thiazole-Containing Compound with Therapeutic Activity in Huntington's Disease Models. / Quinti, Luisa; Casale, Malcolm; Moniot, Sébastien et al.
Em: Cell Chemical Biology, Vol. 23, N.º 7, 21.07.2016, p. 849-861.

Resultado de pesquisa: ???type-name??? › ???researchoutput.researchoutputtypes.contributiontojournal.article??? › revisão de pares

TY - JOUR

T1 - SIRT2- and NRF2-Targeting Thiazole-Containing Compound with Therapeutic Activity in Huntington's Disease Models

AU - Quinti, Luisa

AU - Casale, Malcolm

AU - Moniot, Sébastien

AU - Pais, Teresa F.

AU - Van Kanegan, Michael J.

AU - Kaltenbach, Linda S.

AU - Pallos, Judit

AU - Lim, Ryan G.

AU - Naidu, Sharadha Dayalan

AU - Runne, Heike

AU - Meisel, Lisa

AU - Rauf, Nazifa Abdul

AU - Leyfer, Dmitriy

AU - Maxwell, Michele M.

AU - Saiah, Eddine

AU - Landers, John E.

AU - Luthi-Carter, Ruth

AU - Abagyan, Ruben

AU - Dinkova-Kostova, Albena T.

AU - Steegborn, Clemens

AU - Marsh, J. Lawrence

AU - Lo, Donald C.

AU - Thompson, Leslie M.

AU - Kazantsev, Aleksey G.

PY - 2016/7/21

Y1 - 2016/7/21

N2 - There are currently no disease-modifying therapies for the neurodegenerative disorder Huntington's disease (HD). This study identified novel thiazole-containing inhibitors of the deacetylase sirtuin-2 (SIRT2) with neuroprotective activity in ex vivo brain slice and Drosophila models of HD. A systems biology approach revealed an additional SIRT2-independent property of the lead-compound, MIND4, as an inducer of cytoprotective NRF2 (nuclear factor-erythroid 2 p45-derived factor 2) activity. Structure-activity relationship studies further identified a potent NRF2 activator (MIND4-17) lacking SIRT2 inhibitory activity. MIND compounds induced NRF2 activation responses in neuronal and non-neuronal cells and reduced production of reactive oxygen species and nitrogen intermediates. These drug-like thiazole-containing compounds represent an exciting opportunity for development of multi-targeted agents with potentially synergistic therapeutic benefits in HD and related disorders.

AB - There are currently no disease-modifying therapies for the neurodegenerative disorder Huntington's disease (HD). This study identified novel thiazole-containing inhibitors of the deacetylase sirtuin-2 (SIRT2) with neuroprotective activity in ex vivo brain slice and Drosophila models of HD. A systems biology approach revealed an additional SIRT2-independent property of the lead-compound, MIND4, as an inducer of cytoprotective NRF2 (nuclear factor-erythroid 2 p45-derived factor 2) activity. Structure-activity relationship studies further identified a potent NRF2 activator (MIND4-17) lacking SIRT2 inhibitory activity. MIND compounds induced NRF2 activation responses in neuronal and non-neuronal cells and reduced production of reactive oxygen species and nitrogen intermediates. These drug-like thiazole-containing compounds represent an exciting opportunity for development of multi-targeted agents with potentially synergistic therapeutic benefits in HD and related disorders.

UR - https://www.scopus.com/pages/publications/84978757596

U2 - 10.1016/j.chembiol.2016.05.015

DO - 10.1016/j.chembiol.2016.05.015

M3 - Article

C2 - 27427231

AN - SCOPUS:84978757596

SN - 2451-9456

VL - 23

SP - 849

EP - 861

JO - Cell Chemical Biology

JF - Cell Chemical Biology

IS - 7

ER -

SIRT2- and NRF2-Targeting Thiazole-Containing Compound with Therapeutic Activity in Huntington's Disease Models

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