Evidence map›Paper›PMID 26784451›Full record

ArticlePloS one2016

Hypothyroidism Side Effect in Patients Treated with Sunitinib or Sorafenib: Clinical and Structural Analyses.

Mao Shu, Xiaoli Zai, Beina Zhang, Rui Wang, Zhihua Lin

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
4.1field-weighted citation impact, top 6% 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

15 citing papers in PubMed, 31 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. A retrospective study of proteinuria in dogs receiving toceranib phosphate.The Canadian veterinary journal = La revue veterinaire canadienne · 2018
    Article
  8. Hypothyroidism.Lancet (London, England) · 2017
    Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. 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

5 authors at 2 institutions in 1 country.

Mao ShuSchool of Pharmacy and Bioengineering, Chongqing University of Technology, Chongqing 400054, China.
Xiaoli ZaiSchool of Pharmacy and Bioengineering, Chongqing University of Technology, Chongqing 400054, China.
Beina ZhangSchool of Pharmacy and Bioengineering, Chongqing University of Technology, Chongqing 400054, China.
Rui WangSchool of Pharmacy and Bioengineering, Chongqing University of Technology, Chongqing 400054, China.
Zhihua LinSchool of Pharmacy and Bioengineering, Chongqing University of Technology, Chongqing 400054, China.
Chongqing University of Technology · CNChongqing University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tyrosine kinase inhibitors (TKIs) provide more effective targeted treatments for cancer, but are subject to a variety of adverse effects, such as hypothyroidism. TKI-induced hypothyroidism is a highly complicated issue, because of not only the unrealized toxicological mechanisms, but also different incidences of individual TKI drugs. While sunitinib is suspected for causing thyroid dysfunction more often than other TKIs, sorafenib is believed to be less risky. Here we integrated clinical data and in silico drug-protein interactions to examine the pharmacological distinction between sunitinib and sorafenib. Statistical analysis on the FDA Adverse Event Reporting System (FAERS) confirmed that sunitinib is more concurrent with hypothyroidism than sorafenib, which was observed in both female and male patients. Then, we used docking method and identified 3 proteins specifically binding to sunitinib but not sorafenib, i.e., retinoid X receptor alpha, retinoic acid receptors beta and gamma. As potential off-targets of sunitinib, these proteins are well known to assemble with thyroid hormone receptors, which can explain the profound impact of sunitinib on thyroid function. Taken together, we established a strategy of integrated analysis on clinical records and drug off-targets, which can be applied to explore the molecular basis of various adverse drug reactions.

Indexed as

Carcinoma, Renal CellFemaleHumansHypothyroidismIndolesKidney NeoplasmsMaleModels, MolecularMolecular Docking SimulationNiacinamidePhenylurea CompoundsProtein Kinase InhibitorsPyrrolesReceptors, Retinoic AcidRetinoic Acid Receptor gammaRetinoid X Receptor alphaIndolesNiacinamidePhenylurea CompoundsProtein Kinase InhibitorsPyrrolesReceptors, Retinoic Acidretinoic acid receptor betaRetinoic Acid Receptor gammaRetinoid X Receptor alphaSorafenibSunitinib

Identifiers

PMID26784451
PMCPMC4718448
OpenAlexW2409277720

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.