Evidence map›Paper›PMID 23453837›Full record

ReviewBioorganic & medicinal chemistry letters2013

Heat shock proteins 27, 40, and 70 as combinational and dual therapeutic cancer targets.

Jeanette R McConnell, Shelli R McAlpine

Open access · greenAbstract readReview
In one paragraph

Review in Bioorganic & medicinal chemistry letters, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
5.5field-weighted citation impact, top 3% of its field
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

37 citing papers in PubMed, 79 citations in OpenAlex.

  1. Review
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  6. Article
  7. Heat shock proteins and viral infection.Frontiers in immunology · 2022
    Review
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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

2 authors at 1 institution in 1 country.

Jeanette R McConnellDepartment of Chemistry, University of New South Wales, Sydney, NSW 2052, Australia.
Shelli R McAlpine
UNSW Sydney · AU

Funding

Minority Health &Health Disparities International Research Training ProgramT37MD001442 · NIMHD · SAN DIEGO STATE UNIVERSITY · PI PLEMMONS, DENA · 2005 to 2018
$3.3M
Conformational based design and development of antitumor agentsR01CA137873 · NCI · UNIVERSITY OF NEW SOUTH WALES · PI MCALPINE, SHELLI R · 2009 to 2012
$1.3M
MINORITY INTERNATIONAL RESEARCH TRAINING PROGRAM (MIRT)T37TW000067 · FIC · SAN DIEGO STATE UNIVERSITY · PI POZOS, ROBERT S · 1995 to 2004
$1.2M
FIC NIH HHS T37 TW000067NCI NIH HHS 1R01CA137873NCI NIH HHS R01 CA137873NIMHD NIH HHS T37 MD001442
6 · The paper itself

Abstract

The heat shock proteins are essential players in the development of cancer and they are prime therapeutic targets. Targeting multiple hsps in dual therapies decreases the likelihood of drug resistance compared to utilizing mono-therapies. Further, employing an hsp inhibitor in combination with another therapy has proven clinically successful. Examples of efficacious strategies include the inhibition of hsp27, which prevents protein aggregation, controlling hsp40's role as an ATPase modulator, and inhibiting hsp70 from acting as a molecular chaperone. While hsp40 therapies are just in the beginning stages, hsp27 and hsp70 therapies have been successfully used in dual inhibition treatments with hsp90 inhibitors and in combinational therapy with antineoplastic drugs. Both dual and combinatorial therapies show encouraging results when used in treating chemotherapeutically resistant diseases.

Indexed as

AnimalsAntineoplastic Combined Chemotherapy ProtocolsDrug Resistance, NeoplasmHSP27 Heat-Shock ProteinsHSP40 Heat-Shock ProteinsHSP70 Heat-Shock ProteinsHumansNeoplasmsStructure-Activity RelationshipHSP27 Heat-Shock ProteinsHSP40 Heat-Shock ProteinsHSP70 Heat-Shock Proteins

Identifiers

PMID23453837
PMCPMC3602338
OpenAlexW2056993297

What OpenQuestion holds

Textmetadata
LicenceTDM
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.