Evidence map›Paper›PMID 22120678›Full record

ReviewBiochemical pharmacology2012

Hsp90 inhibitors and drug resistance in cancer: the potential benefits of combination therapies of Hsp90 inhibitors and other anti-cancer drugs.

Xiangyi Lu, Li Xiao, Luan Wang, Douglas M Ruden

Open access · greenAbstract readReview
In one paragraph

Review in Biochemical pharmacology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 64 papers.

0numbers the graph read from it
0cells of the map it votes in
64citing papers in PubMed
3.7field-weighted citation impact, top 6% 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

64 citing papers in PubMed, 113 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Review
  9. Review
  10. Review
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. Article

4 more citing papers are in PubMed but not listed here.

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

4 authors at 2 institutions in 1 country.

Xiangyi LuInstitute of Environmental Health Sciences, Wayne State University, Detroit, MI 48201, United States.
Li Xiao
Luan Wang
Douglas M Ruden
Wayne State University · USUniversity of Alabama at Birmingham · US

Funding

QTL AND MICROARRAY MAPPING LEAD SENSITIVITY GENESR01ES012933 · NIEHS · WAYNE STATE UNIVERSITY · PI RUDEN, DOUGLAS M · 2004 to 2015
$3.4M
Regulation of Signaling of PKD2 Cation Channel in SpermR01DK071073 · NIDDK · WAYNE STATE UNIVERSITY · PI LU, XIANGYI · 2006 to 2009
$1.2M
Effects of Lead on Neuronal Differentiation in Human Embryonic Stem CellsR21ES021983 · NIEHS · WAYNE STATE UNIVERSITY · PI RUDEN, DOUGLAS M · 2012 to 2013
$413k
NIDDK NIH HHS DK071073NIDDK NIH HHS R01 DK071073NIEHS NIH HHS R01 ES012933NIEHS NIH HHS R01ES012933NIEHS NIH HHS R21 ES021983
6 · The paper itself

Abstract

Hsp90 is a chaperone protein that interacts with client proteins that are known to be in the cell cycle, signaling and chromatin-remodeling pathways. Hsp90 inhibitors act additively or synergistically with many other drugs in the treatment of both solid tumors and leukemias in murine tumor models and humans. Hsp90 inhibitors potentiate the actions of anti-cancer drugs that target Hsp90 client proteins, including trastuzumab (Herceptin™) which targets Her2/Erb2B, as Hsp90 inhibition elicits the drug effects in cancer cell lines that are otherwise resistant to the drug. A phase II study of the Hsp90 inhibitor 17-AAG and trastuzumab showed that this combination therapy has anticancer activity in patients with HER2-positive metastatic breast cancer progressing on trastuzumab. In this review, we discuss the results of Hsp90 inhibitors in combination with trastuzumab and other cancer drugs. We also discuss recent results from yeast focused on the genetics of drug resistance when Hsp90 is inhibited and the implications that this might have in understanding the effects of genetic variation in treating cancer in humans.

Indexed as

Drug Resistance, NeoplasmAntibodies, Monoclonal, HumanizedAntineoplastic AgentsAntineoplastic Combined Chemotherapy ProtocolsBenzoquinonesBreast NeoplasmsCisplatinCombined Modality TherapyCysteine Proteinase InhibitorsFemaleHistone Deacetylase InhibitorsHSP90 Heat-Shock ProteinsHumansLactams, MacrocyclicNeoplasmsProteasome InhibitorsAntibodies, Monoclonal, HumanizedAntineoplastic AgentsBenzoquinonesCisplatinCysteine Proteinase InhibitorsHistone Deacetylase InhibitorsHSP90 Heat-Shock ProteinsLactams, MacrocyclicProteasome InhibitorstanespimycinTaxoidsTNF-Related Apoptosis-Inducing LigandTNFSF10 protein, humanTrastuzumab

Identifiers

PMID22120678
PMCPMC3299878
OpenAlexW1972731714

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.