Evidence map›Paper›PMID 31196889›Full record

ArticleMolecular cancer therapeutics2019

Combinatorial Therapy of Zinc Metallochaperones with Mutant p53 Reactivation and Diminished Copper Binding.

Saif Zaman, Xin Yu, Anthony F Bencivenga, Adam R Blanden, Yue Liu, Tracy Withers, Bing Na, Alan J Blayney, John Gilleran, David A Boothman and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in Molecular cancer therapeutics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 1 pooled it
1.6field-weighted citation impact, top 19% 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

25 citing papers in PubMed, 1 synthesis or guideline pooled it, 31 citations in OpenAlex.

  1. Targeting p53 pathways: mechanisms, structures, and advances in therapy.Signal transduction and targeted therapy · 2023
    Pooled it
  2. Journal of enzyme inhibition and medicinal chemistry · 2026
    Article
  3. Article
  4. Review
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  6. Review
  7. Review
  8. Article
  9. Review
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  11. Novel insights into cuproptosis inducers and inhibitors.Frontiers in molecular biosciences · 2024
    Review
  12. Alzheimer's Disease and Cancer: Common Targets.Mini reviews in medicinal chemistry · 2024
    Review
  13. Article
  14. Article
  15. Small-molecule correctors and stabilizers to target p53.Trends in pharmacological sciences · 2023
    Review
  16. Review
  17. Article
  18. A role for bioinorganic chemistry in the reactivation of mutant p53 in cancer.Journal of biological inorganic chemistry : JBIC : a publication of the Society of Biological Inorganic Chemistry · 2022
    Review
  19. p53 and Zinc: A Malleable Relationship.Frontiers in molecular biosciences · 2022
    Review
  20. Review
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

13 authors at 3 institutions in 2 countries.

Saif Zaman *Department of Molecular Biology, Rutgers University, Piscataway, New Jersey.
Xin Yu *Program of Surgical Oncology, Rutgers Cancer Institute of New Jersey, Rutgers University, New Brunswick, New Jersey.
Anthony F BencivengaDepartment of Medicinal Chemistry, Rutgers Ernest Mario School of Pharmacy, Rutgers University, Piscataway, New Jersey.
Adam R BlandenDepartment of Biochemistry and Molecular Biology, SUNY Upstate Medical University, Syracuse, New York.
Yue LiuProgram of Surgical Oncology, Rutgers Cancer Institute of New Jersey, Rutgers University, New Brunswick, New Jersey.
Tracy WithersProgram of Surgical Oncology, Rutgers Cancer Institute of New Jersey, Rutgers University, New Brunswick, New Jersey.
Bing NaProgram of Surgical Oncology, Rutgers Cancer Institute of New Jersey, Rutgers University, New Brunswick, New Jersey.
Alan J BlayneyDepartment of Biochemistry and Molecular Biology, SUNY Upstate Medical University, Syracuse, New York.
John GilleranDepartment of Medicinal Chemistry, Rutgers Ernest Mario School of Pharmacy, Rutgers University, Piscataway, New Jersey.ORCID 0000-0001-6797-8968
David A BoothmanSimmons Comprehensive Cancer Center, University of Texas Southwestern Medical Center, Dallas, Texas.
Stewart N LohDepartment of Biochemistry and Molecular Biology, SUNY Upstate Medical University, Syracuse, New York.
S David KimballDepartment of Medicinal Chemistry, Rutgers Ernest Mario School of Pharmacy, Rutgers University, Piscataway, New Jersey.
Darren R CarpizoProgram of Surgical Oncology, Rutgers Cancer Institute of New Jersey, Rutgers University, New Brunswick, New Jersey. carpizdr@cinj.rutgers.edu.
Rutgers, The State University of New Jersey · USSUNY Upstate Medical University · USThe University of Texas Southwestern Medical Center · US

Funding

Development of Zinc Metallochaperones as Mutant p53 Targeted Anti-cancerDrugsR01CA200800 · NCI · UNIVERSITY OF ROCHESTER · PI CARPIZO, DARREN RICHARD · 2016 to 2020
$1.9M
Exploration of a Mutant p53 Reactivating CompoundK08CA172676 · NCI · RBHS -CANCER INSTITUTE OF NEW JERSEY · PI CARPIZO, DARREN RICHARD · 2013 to 2017
$745k
Restoring the Missing Zinc: A quantitative investigation of p53 hotspot mutant reactivation by synthetic metallochaperones for cancer chemotherapyF30GM113299 · NIGMS · UPSTATE MEDICAL UNIVERSITY · PI BLANDEN, ADAM · 2015 to 2016
$65k
NCI NIH HHS K08 CA172676NCI NIH HHS R01 CA200800NIGMS NIH HHS F30 GM113299
6 · The paper itself

Abstract

Chemotherapy and radiation are more effective in wild-type (WT) p53 tumors due to p53 activation. This is one rationale for developing drugs that reactivate mutant p53 to synergize with chemotherapy and radiation. Zinc metallochaperones (ZMC) are a new class of mutant p53 reactivators that restore WT structure and function to zinc-deficient p53 mutants. We hypothesized that the thiosemicarbazone, ZMC1, would synergize with chemotherapy and radiation. Surprisingly, this was not found. We explored the mechanism of this and found the reactive oxygen species (ROS) activity of ZMC1 negates the signal on p53 that is generated with chemotherapy and radiation. We hypothesized that a zinc scaffold generating less ROS would synergize with chemotherapy and radiation. The ROS effect of ZMC1 is generated by its chelation of redox active copper. ZMC1 copper binding (

Indexed as

MutationAnimalsAntineoplastic AgentsCell LineCombined Modality TherapyCopperHumansMetallochaperonesMiceProtein BindingPyridinesRadiationReactive Oxygen SpeciesSignal TransductionTranscriptional ActivationTumor Suppressor Protein p53Antineoplastic AgentsCopperMetallochaperonesNSC319726PyridinesReactive Oxygen SpeciesTumor Suppressor Protein p53Zinc

Identifiers

PMID31196889
PMCPMC6677634
OpenAlexW2952580407

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.