Evidence map›Paper›PMID 28207175›Full record

ArticleChemistry (Weinheim an der Bergstrasse, Germany)2017

Design of Allosteric Stimulators of the Hsp90 ATPase as New Anticancer Leads.

Ilda D'Annessa, Sara Sattin, Jiahui Tao, Marzia Pennati, Carlos Sànchez-Martìn, Elisabetta Moroni, Andrea Rasola, Nadia Zaffaroni, David A Agard, Anna Bernardi and 1 more

Abstract read
In one paragraph

Article in Chemistry (Weinheim an der Bergstrasse, Germany), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

14 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Design of Disruptors of the Hsp90-Cdc37 Interface.Molecules (Basel, Switzerland) · 2020
    Article
  7. Review
  8. Article
  9. Review
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Ilda D'AnnessaIstituto di Chimica del Riconoscimento Molecolare, CNR, via Mario Bianco, 9, 20131, Milan, Italy.
Sara SattinDipartimento di Chimica, Università degli Studi di Milano, via Golgi, 19, 20133, Milan, Italy.
Jiahui TaoHoward Hughes Medical Institute and Dept. of Biochemistry & Biophysics, University of California, 600 16thStreet, San Francisco, CA, 94158, USA.
Marzia PennatiDept. Experimental Oncology & Molecular Medicine, Molecular Pharmacology Unit, Fondazione IRCCS Istituto Nazionale dei Tumori, via Amadeo, 42, 20133, Milano, Italy.
Carlos Sànchez-MartìnDipartimento di Scienze Biomediche-DSB, Università di Padova, Via Ugo Bassi 58/B, 35131, Padova, Italy.
Elisabetta MoroniIRCCS Multimedica, via Fantoli 16/15, 20138, Milano, Italy.
Andrea RasolaDipartimento di Scienze Biomediche-DSB, Università di Padova, Via Ugo Bassi 58/B, 35131, Padova, Italy.
Nadia ZaffaroniDept. Experimental Oncology & Molecular Medicine, Molecular Pharmacology Unit, Fondazione IRCCS Istituto Nazionale dei Tumori, via Amadeo, 42, 20133, Milano, Italy.
David A AgardHoward Hughes Medical Institute and Dept. of Biochemistry & Biophysics, University of California, 600 16thStreet, San Francisco, CA, 94158, USA.
Anna BernardiDipartimento di Chimica, Università degli Studi di Milano, via Golgi, 19, 20133, Milan, Italy.ORCID http://orcid.org/0000-0002-1258-2007
Giorgio ColomboIstituto di Chimica del Riconoscimento Molecolare, CNR, via Mario Bianco, 9, 20131, Milan, Italy.ORCID http://orcid.org/0000-0002-1318-668X

Funding

Howard Hughes Medical Institute
6 · The paper itself

Abstract

Allosteric compounds that stimulate Hsp90 adenosine triphosphatase (ATPase) activity were rationally designed, showing anticancer potencies in the low micromolar to nanomolar range. In parallel, the mode of action of these compounds was clarified and a quantitative model that links the dynamic ligand-protein cross-talk to observed cellular and in vitro activities was developed. The results support the potential of using dynamics-based approaches to develop original mechanism-based cancer therapeutics.

Indexed as

Adenosine TriphosphatasesAllosteric RegulationAntineoplastic AgentsDrug DesignHSP90 Heat-Shock ProteinsLigandsProtein BindingAdenosine TriphosphatasesAntineoplastic AgentsHSP90 Heat-Shock ProteinsLigandsallosterydrug designhsp90modulatorsmolecular dynamics

Identifiers

PMID28207175
PMCPMC5927549

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.