Evidence map›Paper›PMID 20337575›Full record

ReviewCurrent pharmaceutical design2010

Novel metals and metal complexes as platforms for cancer therapy.

Michael Frezza, Sarmad Hindo, Di Chen, Andrew Davenport, Sara Schmitt, Dajena Tomco, Q Ping Dou

Abstract readReview
In one paragraph

Review in Current pharmaceutical design, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 132 papers.

0numbers the graph read from it
0cells of the map it votes in
132citing papers in PubMed
4.8field-weighted citation impact, top 4% 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

132 citing papers in PubMed, 534 citations in OpenAlex.

  1. Article
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  4. Review
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  6. Holography Meets Theranostics: DFT/TDDFT Insights into Ru-NO@MInternational journal of molecular sciences · 2025
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72 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

7 authors at 1 institution in 1 country.

Michael FrezzaBarbara Ann Karmanos Cancer Institute, Department of Oncology and Pathology, School of Medicine, Wayne State University, Detroit, Michigan 48201, USA.
Sarmad Hindo
Di Chen
Andrew Davenport
Sara Schmitt
Dajena Tomco
Q Ping Dou
Wayne State University · US

Funding

TRAINING PROGRAM IN THE BIOLOGY OF CANCERT32CA009531 · NCI · WAYNE STATE UNIVERSITY · PI Larry H Matherly · 1985 to 2026
$5.3M
Roles of polymorphic COMT, tea polyphenols and proteasome in cancer preventionR01CA120009 · NCI · WAYNE STATE UNIVERSITY · PI DOU, QING PING · 2006 to 2010
$1.5M
High resolution spectroscopy for in vivo copper speciation in prostate and breastR21CA139386 · NCI · ILLINOIS INSTITUTE OF TECHNOLOGY · PI BARREA, RAUL ALBERTO · 2009 to 2010
$334k
NCI NIH HHS 1R01CA120009NCI NIH HHS 1R21CA139386-01NCI NIH HHS 3R01CA120009-04S1NCI NIH HHS R01 CA120009NCI NIH HHS R21 CA139386NCI NIH HHS T32 CA009531NCI NIH HHS T32-CA009531
6 · The paper itself

Abstract

Metals are essential cellular components selected by nature to function in several indispensable biochemical processes for living organisms. Metals are endowed with unique characteristics that include redox activity, variable coordination modes, and reactivity towards organic substrates. Due to their reactivity, metals are tightly regulated under normal conditions and aberrant metal ion concentrations are associated with various pathological disorders, including cancer. For these reasons, coordination complexes, either as drugs or prodrugs, become very attractive probes as potential anticancer agents. The use of metals and their salts for medicinal purposes, from iatrochemistry to modern day, has been present throughout human history. The discovery of cisplatin, cis-[Pt(II) (NH(3))(2)Cl(2)], was a defining moment which triggered the interest in platinum(II)- and other metal-containing complexes as potential novel anticancer drugs. Other interests in this field address concerns for uptake, toxicity, and resistance to metallodrugs. This review article highlights selected metals that have gained considerable interest in both the development and the treatment of cancer. For example, copper is enriched in various human cancer tissues and is a co-factor essential for tumor angiogenesis processes. However the use of copper-binding ligands to target tumor copper could provide a novel strategy for cancer selective treatment. The use of nonessential metals as probes to target molecular pathways as anticancer agents is also emphasized. Finally, based on the interface between molecular biology and bioinorganic chemistry the design of coordination complexes for cancer treatment is reviewed and design strategies and mechanisms of action are discussed.

Indexed as

Drug DesignAnimalsAntineoplastic AgentsChelating AgentsCoordination ComplexesCopperGalliumHumansMetalsNeovascularization, PathologicNickelOrganometallic CompoundsPlatinum CompoundsProteasome Endopeptidase ComplexProteasome InhibitorsUbiquitinationAntineoplastic AgentsChelating AgentsCoordination ComplexesCopperGalliumMetalsNickelOrganometallic CompoundsPlatinum CompoundsProteasome Endopeptidase ComplexProteasome InhibitorsZinc Compounds

Identifiers

PMID20337575
PMCPMC3759287
OpenAlexW2124736536

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.