Evidence map›Paper›PMID 24180275›Full record

ReviewCurrent medicinal chemistry2014

Targeting MDM2-p53 interaction for cancer therapy: are we there yet?

S Nag, X Zhang, K S Srivenugopal, M-H Wang, W Wang, R Zhang

Open access · bronzeAbstract readReview
In one paragraph

Review in Current medicinal chemistry, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 87 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
87citing papers in PubMed, 2 pooled it
5.7field-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

87 citing papers in PubMed, 2 syntheses or guidelines pooled it, 143 citations in OpenAlex.

  1. Resisting Resistance to Immune Checkpoint Therapy: A Systematic Review.International journal of molecular sciences · 2020
    Pooled it
  2. Pooled it
  3. Role of the MDM2/p53 axis in regulating cisplatin response in tumor cells.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    Review
  4. Therapeutic peptides and proteins: Status and developments in drug delivery.Journal of controlled release : official journal of the Controlled Release Society · 2026
    Review
  5. Review
  6. Review
  7. Article
  8. Review
  9. Article
  10. Review
  11. Review
  12. Frontiers in chemistry · 2025
    Article
  13. Review
  14. p53 and the E3 Ubiquitin Ligase MDM2 in Glaucomatous Lamina Cribrosa Cells.International journal of molecular sciences · 2024
    Article
  15. Article
  16. Review
  17. Review
  18. Review
  19. Review
  20. Review

27 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

6 authors at 2 institutions in 1 country.

S Nag
X Zhang
K S Srivenugopal
M-H Wang
W Wang
R ZhangDepartment of Pharmaceutical Sciences, School of Pharmacy, Texas Tech University Health Sciences Center, 1300 S Coulter Street, Amarillo, TX 79106, USA. ruiwen.zhang@ttuhsc.edu.
Texas Tech University · USTexas Tech University Health Sciences Center · US

Funding

Novel Small Molecule MDM2 Inhibitors for Pancreatic Cancer TherapyR01CA186662 · NCI · UNIVERSITY OF HOUSTON · PI ZHANG, RUIWEN · 2014 to 2018
$2.4M
Dietary Chemopreventive Components/Oncogene Interaction and CancerR01CA121211 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI ZHANG, RUIWEN · 2007 to 2011
$1.4M
MDM2 AS A NEGATIVE REGULATOR OF P21 WAF1/CIP1R01CA112029 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI ZHANG, RUIWEN · 2005 to 2009
$1.3M
NCI NIH HHS R01 CA112029NCI NIH HHS R01 CA121211NCI NIH HHS R01 CA186662
6 · The paper itself

Abstract

Inactivation of the tumor suppressor p53 and/or overexpression of the oncogene MDM2 frequently occur in human cancers, and are associated with poor prognosis, advanced forms of the disease, and chemoresistance. MDM2, the major negative regulator of p53, induces p53 degradation and inactivates its tumor suppressing activity. In turn, p53 regulates MDM2 expression. This MDM2-p53 negative feedback loop has been widely studied and presents an attractive target for cancer therapy, with a few of the inhibitors of this interaction already having advanced into clinical trials. Additionally, there is an increasing interest in understanding MDM2's p53-independent activities in carcinogenesis and cancer progression, which may also have implications for cancer therapy. This review aims to highlight the various roles that the MDM2-p53 interaction plays in cancer, the p53 independent oncogenic activities of MDM2 and the various strategies that may be used to target MDM2 and the MDM2-p53 interaction. We will summarize the major preclinical and clinical evidences of MDM2 inhibitors for human cancer treatment and make suggestions to further improve efficacy and safety of this interesting class of cancer therapeutics.

Indexed as

Antineoplastic AgentsClinical Trials as TopicHumansImidazolinesIndolesNeoplasmsProtein Interaction Domains and MotifsProto-Oncogene Proteins c-mdm2Small Molecule LibrariesTryptaminesTumor Suppressor Protein p53Antineoplastic AgentsImidazolinesIndolesMDM2 protein, humanProto-Oncogene Proteins c-mdm2Small Molecule LibrariestryptamineTryptaminesTumor Suppressor Protein p53

Identifiers

PMID24180275
PMCPMC6690199
OpenAlexW2059777480

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.