Evidence map›Paper›PMID 28508231›Full record

ReviewArchives of toxicology2017

Role of the aryl hydrocarbon receptor in carcinogenesis and potential as an anti-cancer drug target.

Siva Kumar Kolluri, Un-Ho Jin, Stephen Safe

Erratum issuedOpen access · greenAbstract readReview
In one paragraph

Review in Archives of toxicology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 89 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
89citing papers in PubMed, 2 pooled it
11.0field-weighted citation impact, top 1% 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

89 citing papers in PubMed, 2 syntheses or guidelines pooled it, 175 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Article
  5. Endocrine Disruptors and Gynecological Malignancies.Diagnostics (Basel, Switzerland) · 2026
    Review
  6. Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. AhR and STAT3: A Dangerous Duo in Chemical Carcinogenesis.International journal of molecular sciences · 2025
    Review
  15. Review
  16. Review
  17. Article
  18. Article
  19. Article
  20. Article

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors at 2 institutions in 1 country.

Siva Kumar KolluriDepartment of Environmental and Molecular Toxicology, Oregon State University, Corvallis, OR, 97331, USA.
Un-Ho JinDepartment of Veterinary Physiology and Pharmacology, Texas A & M University, 4466 TAMU, College Station, TX, 77843, USA.
Stephen SafeDepartment of Veterinary Physiology and Pharmacology, Texas A & M University, 4466 TAMU, College Station, TX, 77843, USA. ssafe@cvm.tamu.edu.ORCID http://orcid.org/0000-0002-2115-3060
Texas A&M University · USOregon State University · US

Funding

TARGETED GENOMICS FACILITY COREP30ES023512 · NIEHS · TEXAS A&M AGRILIFE RESEARCH · PI THREADGILL, DAVID W. · 2014 to 2017
$3.3M
Diet induced modifications of microbiota metabolites in colon tumorigenesisR01CA202697 · NCI · TEXAS A&M AGRILIFE RESEARCH · PI ALLRED, CLINTON D, CHAPKIN, ROBERT STEPHEN · 2016 to 2020
$2.0M
Cytosolic Ah Receptor: Mechanism of ActionR21ES025839 · NIEHS · TEXAS A&M AGRILIFE RESEARCH · PI SAFE, STEPHEN H. · 2015 to 2016
$399k
NCI NIH HHS R01 CA202697NIEHS NIH HHS P30 ES023512NIEHS NIH HHS R21 ES025839
6 · The paper itself

Abstract

The aryl hydrocarbon receptor (AhR) was initially identified as the receptor that binds and mediates the toxic effects induced by 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) and structurally related halogenated aromatics. Other toxic compounds including some polynuclear aromatic hydrocarbons act through the AhR; however, during the last 25 years, it has become apparent that the AhR plays an essential role in maintaining cellular homeostasis. Moreover, the scope of ligands that bind the AhR includes endogenous compounds such as multiple tryptophan metabolites, other endogenous biochemicals, pharmaceuticals and health-promoting phytochemicals including flavonoids, indole-3-carbinol and its metabolites. It has also been shown that like other receptors, the AhR is a drug target for multiple diseases including cancer, where both AhR agonists and antagonists effectively block many of the critical hallmarks of cancer in multiple tumor types. This review describes the anti-cancer activities of AhR ligands and demonstrates that it is time to separate the AhR from TCDD and exploit the potential of the AhR as a novel target for cancer chemotherapy.

Indexed as

Antineoplastic AgentsHumansMolecular Targeted TherapyNeoplasmsNeoplastic Stem CellsPolychlorinated DibenzodioxinsReceptors, Aryl HydrocarbonAntineoplastic AgentsPolychlorinated DibenzodioxinsReceptors, Aryl HydrocarbonAh receptorCancerDrug targetLigands

Identifiers

PMID28508231
PMCPMC6357772
OpenAlexW2614737589

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.