Evidence map›Paper›PMID 24019973›Full record

ArticlePloS one2013

Inhibition of STAT3 by niclosamide synergizes with erlotinib against head and neck cancer.

Rui Li, Shuo You, Zhongliang Hu, Zhuo G Chen, Gabriel L Sica, Fadlo R Khuri, Walter J Curran, Dong M Shin, Xingming Deng

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed
4.2field-weighted citation impact, top 5% 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

49 citing papers in PubMed, 87 citations in OpenAlex.

  1. Trial
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  3. PTPN9 dephosphorylates IGF1RJournal of experimental & clinical cancer research : CR · 2025
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  10. Salicylanilides and Their Anticancer Properties.International journal of molecular sciences · 2023
    Review
  11. Article
  12. Article
  13. Niclosamide-A promising treatment for COVID-19.British journal of pharmacology · 2022
    Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Trefoil Factor 3 Inhibits Thyroid Cancer Cell Progression Related to IL-6/JAK/STAT3 Signaling Pathway.Evidence-based complementary and alternative medicine : eCAM · 2021
    Article
  19. 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

9 authors at 1 institution in 1 country.

Rui LiDepartment of Radiation Oncology, Emory University School of Medicine and Winship Cancer Institute, Emory University, Atlanta, Georgia, United States of America.
Shuo You
Zhongliang Hu
Zhuo G Chen
Gabriel L Sica
Fadlo R Khuri
Walter J Curran
Dong M Shin
Xingming Deng
Emory University · US

Funding

TARGETING DEATH RECEPTOR-MEDIATED APOPTOSIS FOR HEAD AND NECK CANCERP50CA128613 · NCI · EMORY UNIVERSITY · PI SHIN, DONG M · 2007 to 2011
$12.0M
Structure-based anti-cancer drug developmentR01CA136534 · NCI · EMORY UNIVERSITY · PI DENG, XINGMING · 2010 to 2020
$3.4M
Developing a Platform for Prediction of Metastasis Using Multiplexed QD-imagingR33CA161873 · NCI · EMORY UNIVERSITY · PI CHEN, ZHUO GEORGIA, HOYT, CLIFFORD C · 2011 to 2013
$960k
NCI NIH HHS CA128613NCI NIH HHS P50 CA128613NCI NIH HHS R01 CA136534NCI NIH HHS R01CA136534NCI NIH HHS R33 CA161873
6 · The paper itself

Abstract

Epidermal growth factor receptor (EGFR) is extensively expressed in head and neck cancer. However, EGFR-targeted therapy has only modest efficacy in head and neck cancer, through mechanisms that are not fully understood. Here, we found that inhibition of EGFR by erlotinib stimulated phosphorylation and activation of STAT3 leading to increased Bcl2/Bcl-XL expression in head and neck cancer cells, which may dampen the therapeutic efficacy of erlotinib against head and neck cancer. Erlotinib-enhanced STAT3 phosphorylation results, at least in part, from suppression of its physiological phosphatase, PTPMeg2. Specific knockdown of STAT3 by RNA interference significantly sensitized head and neck cancer cells to erlotinib treatment. Pharmacological inhibition of STAT3 by niclosamide not only blocked erlotinib-stimulated STAT3 phosphorylation but also synergistically repressed head and neck cancer growth in vitro and in vivo. Combined inhibition of EGFR and STAT3 by erlotinib and niclosamide more effectively induced apoptosis in tumor tissues without toxicity for normal tissues. Based on our findings, treatment with erlotinib combined with niclosamide may offer an effective therapeutic approach to improve the prognosis of head and neck cancer.

Indexed as

Antineoplastic AgentsBase SequenceCell Line, TumorDNA PrimersDrug SynergismErbB ReceptorsErlotinib HydrochlorideHead and Neck NeoplasmsHumansNiclosamidePhosphorylationQuinazolinesReverse Transcriptase Polymerase Chain ReactionSTAT3 Transcription FactorAntineoplastic AgentsDNA PrimersErbB ReceptorsErlotinib HydrochlorideNiclosamideQuinazolinesSTAT3 protein, humanSTAT3 Transcription Factor

Identifiers

PMID24019973
PMCPMC3760825
OpenAlexW2001309836

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.