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@article{04e6e21b52f44067ba6de6b941c8dd79,
title = "New inhibitor targeting human transcription factor HSF1: effects on the heat shock response and tumour cell survival.",
abstract = "Comparative modeling of the DNA-binding domain of human HSF1 facilitated the prediction of possible binding pockets for small molecules and definitionof corresponding pharmacophores. In silico screening of a large library of lead-like compounds identified a set of compounds that satisfied thepharmacophoric criteria, a selection of which compounds was purchased to populate a biased sublibrary. A discriminating cell-based screening assayidentified compound 001, which was subjected to systematic analysis of structure–activity relationships, resulting in the development of compound 115(IHSF115). IHSF115 bound to an isolated HSF1 DNAbinding domain fragment. The compound did not affect heat-induced oligomerization, nuclear localizationand specific DNA binding but inhibited the transcriptional activity of human HSF1, interfering with the assembly of ATF1-containing transcription complexes.IHSF115 was employed to probe the human heat shock response at the transcriptome level. In contrast to earlier studies of differential regulationin HSF1-na¨ıve and -depleted cells, our results suggest that a large majority of heat-induced genes is positively regulated by HSF1. That IHSF115 effectivelycountermanded repression in a significant fraction of heat-repressed genes suggests that repression of these genes is mediated by transcriptionally activeHSF1. IHSF115 is cytotoxic for a variety of human cancer cell lines, multiplemyeloma lines consistently exhibiting high sensitivity.",
keywords = "transcription, genetic, cell survival, DNA, genes, heat (physical force), heat-shock reponse, interleukin-6, neoplasms, transcriptino factor, tumor cells, malignant, molecule",
author = "Stewart Kirton",
note = "{\textcopyright} The Author(s) 2017. Published by Oxford University Press on behalf of Nucleic Acids Research. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com Nuria Vilabo, Alba Bore, Francisco Martin-Saavedra, Melanie Bayford, Natalie Winfield, Stuart Firth-Clark, Stewart B. Kirton, and Richard Voellmy, 'New inhibitor targeting human transcription factor HSF1: effects on the heat shock response and tumor cell survival', Nucleic Acids Research, 2017, 1, doi: 10.1093/nar/gkx194 ",
year = "2017",
month = mar,
day = "21",
doi = "10.1093/nar/gkx194",
language = "English",
journal = "Nucleic Acids Research ",
issn = "0305-1048",
publisher = "Oxford University Press",

}

RIS

TY - JOUR

T1 - New inhibitor targeting human transcription factor HSF1: effects on the heat shock response and tumour cell survival.

AU - Kirton, Stewart

N1 - © The Author(s) 2017. Published by Oxford University Press on behalf of Nucleic Acids Research. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com Nuria Vilabo, Alba Bore, Francisco Martin-Saavedra, Melanie Bayford, Natalie Winfield, Stuart Firth-Clark, Stewart B. Kirton, and Richard Voellmy, 'New inhibitor targeting human transcription factor HSF1: effects on the heat shock response and tumor cell survival', Nucleic Acids Research, 2017, 1, doi: 10.1093/nar/gkx194

PY - 2017/3/21

Y1 - 2017/3/21

N2 - Comparative modeling of the DNA-binding domain of human HSF1 facilitated the prediction of possible binding pockets for small molecules and definitionof corresponding pharmacophores. In silico screening of a large library of lead-like compounds identified a set of compounds that satisfied thepharmacophoric criteria, a selection of which compounds was purchased to populate a biased sublibrary. A discriminating cell-based screening assayidentified compound 001, which was subjected to systematic analysis of structure–activity relationships, resulting in the development of compound 115(IHSF115). IHSF115 bound to an isolated HSF1 DNAbinding domain fragment. The compound did not affect heat-induced oligomerization, nuclear localizationand specific DNA binding but inhibited the transcriptional activity of human HSF1, interfering with the assembly of ATF1-containing transcription complexes.IHSF115 was employed to probe the human heat shock response at the transcriptome level. In contrast to earlier studies of differential regulationin HSF1-na¨ıve and -depleted cells, our results suggest that a large majority of heat-induced genes is positively regulated by HSF1. That IHSF115 effectivelycountermanded repression in a significant fraction of heat-repressed genes suggests that repression of these genes is mediated by transcriptionally activeHSF1. IHSF115 is cytotoxic for a variety of human cancer cell lines, multiplemyeloma lines consistently exhibiting high sensitivity.

AB - Comparative modeling of the DNA-binding domain of human HSF1 facilitated the prediction of possible binding pockets for small molecules and definitionof corresponding pharmacophores. In silico screening of a large library of lead-like compounds identified a set of compounds that satisfied thepharmacophoric criteria, a selection of which compounds was purchased to populate a biased sublibrary. A discriminating cell-based screening assayidentified compound 001, which was subjected to systematic analysis of structure–activity relationships, resulting in the development of compound 115(IHSF115). IHSF115 bound to an isolated HSF1 DNAbinding domain fragment. The compound did not affect heat-induced oligomerization, nuclear localizationand specific DNA binding but inhibited the transcriptional activity of human HSF1, interfering with the assembly of ATF1-containing transcription complexes.IHSF115 was employed to probe the human heat shock response at the transcriptome level. In contrast to earlier studies of differential regulationin HSF1-na¨ıve and -depleted cells, our results suggest that a large majority of heat-induced genes is positively regulated by HSF1. That IHSF115 effectivelycountermanded repression in a significant fraction of heat-repressed genes suggests that repression of these genes is mediated by transcriptionally activeHSF1. IHSF115 is cytotoxic for a variety of human cancer cell lines, multiplemyeloma lines consistently exhibiting high sensitivity.

KW - transcription

KW - genetic

KW - cell survival

KW - DNA

KW - genes

KW - heat (physical force)

KW - heat-shock reponse

KW - interleukin-6

KW - neoplasms

KW - transcriptino factor

KW - tumor cells

KW - malignant

KW - molecule

U2 - 10.1093/nar/gkx194

DO - 10.1093/nar/gkx194

M3 - Article

JO - Nucleic Acids Research

JF - Nucleic Acids Research

SN - 0305-1048

ER -