Fakulteta za farmacijo, Ljubljana (FFALJ)
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Following the design path of isoform-selective Hsp90 inhibitors : small differences, great opportunitiesDernovšek, Jaka ; Tomašič, TihomirThe heat shock protein 90 (Hsp90) family consists of four highly conserved isoforms: the mitochondrial TRAP-1, the endoplasmic reticulum-localised Grp94, and the cytoplasmic Hsp90α and Hsp90β. Since ... the late 1990s, this family has been extensively studied as a potential target for the treatment of cancer, neurological disorders, and infectious diseases. The initial approach was to develop non-selective, so-called pan-Hsp90 ATP-competitive inhibitors of the N-terminal domain. Many of these agents were tested in clinical trials, mainly for the treatment of cancer, but none of them succeeded in the clinic. This was mainly due to the lack of efficacy and various toxicities associated with the induction of heat shock response (HSR). This lack of success has prompted a turn to new approaches of Hsp90 inhibition. Thus, inhibitors selective for a particular isoform of Hsp90 have been developed. These isoform-selective inhibitors do not induce HSR and have a more targeted effect because not all client proteins are equally dependent on all four paralogues of Hsp90. However, it is extremely difficult to develop such selective compounds because the family is highly conserved. Hsp90α and Hsp90β have an amazing 95% identity of the N-terminal ATP binding site, differing only in two amino acid residues. Therefore, the focus of this review is to fully elucidate the key structural features of the selective inhibitor classes in terms of binding site dissimilarities. In addition to a methodological characterisation of the structure-activity relationships, the main advantages of selective inhibition of the TRAP-1, Grp94, Hsp90α and Hsp90β isoforms are discussed.Vir: Pharmacology & therapeutics. - ISSN 0163-7258 (art. 108396, Vol. 245, 2023, str. 1-20)Vrsta gradiva - članek, sestavni del ; neleposlovje za odrasleLeto - 2023Jezik - angleškiCOBISS.SI-ID - 147241219
Avtor
Dernovšek, Jaka |
Tomašič, Tihomir
Teme
Rak (medicina) |
Farmacevtska kemija |
cancer |
drug design |
Hsp90 |
inhibitor |
selectivity |
zasnova zdravila |
selektivnost |
inhibitorji |
Hsp90
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Avtor | Dernovšek, Jaka ; Tomašič, Tihomir |
Naslov | Following the design path of isoform-selective Hsp90 inhibitors : small differences, great opportunities |
Datum objave | 2023-03-29 |
COBISS.SI-ID | 147241219 |
Verzija objave v repozitoriju | Založnikova različica |
Licenca objave v repozitoriju | Creative Commons Priznanje avtorstva 4.0 Mednarodna |
Embargo | Takojšnja javna objava |
Projekti, iz katerih je bila financirana objava
Naziv | Akronim | Številka projekta | Financer |
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Farmacevtska kemija: načrtovanje, sinteza in vrednotenje učinkovin | P1-0208-2022 |
Javna agencija za znanstvenoraziskovalno in inovacijsko dejavnost Republike Slovenije |
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Razvoj novih zaviralcev Hsp90 s protitumornim delovanjem | J1-1717-2019 |
Javna agencija za znanstvenoraziskovalno in inovacijsko dejavnost Republike Slovenije |
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Ime baze podatkov | Področje | Leto |
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Povezave do osebnih bibliografij avtorjev | Povezave do podatkov o raziskovalcih v sistemu SICRIS |
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Dernovšek, Jaka | 54784 |
Tomašič, Tihomir | 28334 |
Vir: Osebne bibliografije
in: SICRIS
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