Evidence map›Paper›PMID 27768592›Full record

SynthesisOncotarget2016

Genetic polymorphisms in leptin, adiponectin and their receptors affect risk and aggressiveness of prostate cancer: evidence from a meta-analysis and pooled-review.

Meng-Bo Hu, Hua Xu, Ji-Meng Hu, Wen-Hui Zhu, Tian Yang, Hao-Wen Jiang, Qiang Ding

Open access · diamondAbstract readMeta-AnalysisReview
In one paragraph

Synthesis in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 3 pooled it
2.4field-weighted citation impact, top 11% 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, 3 syntheses or guidelines pooled it, 24 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Investigation ofBioscience reports · 2019
    Pooled it
  4. Article
  5. Review
  6. Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. Adiponectin: Role in Physiology and Pathophysiology.International journal of preventive medicine · 2020
    Review
  12. Adipose Tissue, Obesity and Adiponectin: Role in Endocrine Cancer Risk.International journal of molecular sciences · 2019
    Review
  13. Review
  14. Article
  15. Role of Adiponectin in prostate cancer.International braz j urol : official journal of the Brazilian Society of Urology
    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

7 authors at 2 institutions in 1 country.

Meng-Bo HuDepartment of Urology, Huashan Hospital, Fudan University, Shanghai 200040, China.
Hua XuDepartment of Urology, Huashan Hospital, Fudan University, Shanghai 200040, China.
Ji-Meng HuDepartment of Urology, Huashan Hospital, Fudan University, Shanghai 200040, China.
Wen-Hui ZhuDepartment of Urology, Huashan Hospital, Fudan University, Shanghai 200040, China.
Tian YangDepartment of Urology, Huashan Hospital, Fudan University, Shanghai 200040, China.
Hao-Wen JiangDepartment of Urology, Huashan Hospital, Fudan University, Shanghai 200040, China.
Qiang DingDepartment of Urology, Huashan Hospital, Fudan University, Shanghai 200040, China.
Fudan University · CNHuashan Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Leptin and adiponectin signaling was associated with development and progression of various cancers. The present study aimed to clarify the role of genetic variants in leptin, adiponectin and their receptors in prostate cancer. After comprehensive search and manuscript scanning, a total of 49 genetic variants were enrolled and examined for their relations to cancer risk and aggressiveness. In the meta-analysis, LEP rs7799039 (allele contrast: OR 1.133, 95%CI 1.024-1.254), ADIPOQ rs2241766 (allele contrast: OR 1.201, 95%CI 1.015-1.422) and ADIPOR1 rs10920531 (allele contrast: OR 1.184, 95%CI 1.075-1.305) variants were identified to be correlated with increased risk of prostate cancer. On the contrary, LEPR rs1137101 (allele contrast: OR 0.843, 95%CI 0.730-0.973) and ADIPOR1 rs2232853 (allele contrast: OR 0.638, 95%CI 0.535-0.760) variants were associated with decreased risk of prostate cancer. From the pooled-review, we additionally recognized eight variants associated with cancer risk and another eight variants associated with cancer aggressiveness, respectively. These observations indicated important roles of leptin, adiponectin and their receptors in the development and progression of prostate cancer. The identified polymorphisms might assist in developing better risk-assessment tools, as well as generating novel targeted therapies, especially for obese cancer patients with impaired leptin and adiponectin signaling.

Indexed as

Polymorphism, Single NucleotideAdiponectinBiomarkers, TumorDisease-Free SurvivalDisease ProgressionGenetic Predisposition to DiseaseHumansLeptinMaleNeoplasm GradingOdds RatioPhenotypeProstatic NeoplasmsReceptors, AdiponectinReceptors, LeptinRisk AssessmentAdiponectinADIPOQ protein, humanADIPOR1 protein, humanBiomarkers, TumorLEPR protein, humanLeptinReceptors, AdiponectinReceptors, Leptinadiponectingenetic polymorphismleptinmeta-analysisprostate cancer

Identifiers

PMID27768592
PMCPMC5348375
OpenAlexW2538253367

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.