Evidence map›Paper›PMID 28915899›Full record

ArticleBMC gastroenterology2017

Association between polymorphisms of TAS2R16 and susceptibility to colorectal cancer.

Jonathan Barontini, Marco Antinucci, Sergio Tofanelli, Maurizio Cammalleri, Massimo Dal Monte, Federica Gemignani, Pavel Vodicka, Roberto Marangoni, Ludmila Vodickova, Juozas Kupcinskas and 11 more

Open access · goldAbstract read
In one paragraph

Article in BMC gastroenterology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 2 pooled it
1.1field-weighted citation impact, top 22% 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

21 citing papers in PubMed, 2 syntheses or guidelines pooled it, 31 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. The Role ofMedicina (Kaunas, Lithuania) · 2020
    Trial
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  7. Review
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  10. Investigating the Potential Influence ofJournal of personalized medicine · 2024
    Article
  11. Article
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  15. Article
  16. Review
  17. An update on extra-oral bitter taste receptors.Journal of translational medicine · 2021
    Review
  18. Review
  19. Article
  20. Analysis of factors potentially predicting prognosis of colorectal cancer.World journal of gastrointestinal oncology · 2019
    Article
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

21 authors at 9 institutions in 5 countries.

Jonathan BarontiniDepartment of Biology, University of Pisa, Via Derna 1, 56100, Pisa, Italy.
Marco AntinucciDepartment of Biology, University of Pisa, Via Derna 1, 56100, Pisa, Italy.
Sergio TofanelliDepartment of Biology, University of Pisa, Via Derna 1, 56100, Pisa, Italy.
Maurizio CammalleriDepartment of Biology, University of Pisa, Via Derna 1, 56100, Pisa, Italy.
Massimo Dal MonteDepartment of Biology, University of Pisa, Via Derna 1, 56100, Pisa, Italy.
Federica GemignaniDepartment of Biology, University of Pisa, Via Derna 1, 56100, Pisa, Italy.
Pavel VodickaDepartment of Molecular Biology of Cancer, Institute of Experimental Medicine, Academy of Science of Czech Republic, Prague, Czech Republic.
Roberto MarangoniDepartment of Biology, University of Pisa, Via Derna 1, 56100, Pisa, Italy.
Ludmila VodickovaDepartment of Molecular Biology of Cancer, Institute of Experimental Medicine, Academy of Science of Czech Republic, Prague, Czech Republic.
Juozas KupcinskasDepartment of Gastroenterology, Lithuanian University of Health Sciences, Kaunas, Lithuania.
Veronika VymetalkovaDepartment of Molecular Biology of Cancer, Institute of Experimental Medicine, Academy of Science of Czech Republic, Prague, Czech Republic.
Asta ForstiGenomic Epidemiology Group, German Cancer Research Center (DKFZ), Heidelberg, Germany.
Federico CanzianDivision of Molecular Genetic Epidemiology, German Cancer Research Center (DKFZ), Heidelberg, Germany.
Angelika SteinDivision of Molecular Genetic Epidemiology, German Cancer Research Center (DKFZ), Heidelberg, Germany.
Victor MorenoCancer Prevention and Control Program, Catalan Institute of Oncology (ICO), IDIBELL, CIBERESP and Department of Clinical Sciences, Faculty of Medicine, University of Barcelona, Barcelona, Spain.
Nicola MastrodonatoDivision of Gastroenterology and Research Laboratory, IRCCS Scientific Institute and Regional General Hospital "Casa Sollievo della Sofferenza", San Giovanni Rotondo, Italy.
Francesca TavanoDivision of Gastroenterology and Research Laboratory, IRCCS Scientific Institute and Regional General Hospital "Casa Sollievo della Sofferenza", San Giovanni Rotondo, Italy.
Anna PanzaDivision of Gastroenterology and Research Laboratory, IRCCS Scientific Institute and Regional General Hospital "Casa Sollievo della Sofferenza", San Giovanni Rotondo, Italy.
Roberto BaraleDepartment of Biology, University of Pisa, Via Derna 1, 56100, Pisa, Italy.
Stefano LandiDepartment of Biology, University of Pisa, Via Derna 1, 56100, Pisa, Italy. stefano.landi@unipi.it.
Daniele CampaDepartment of Biology, University of Pisa, Via Derna 1, 56100, Pisa, Italy.
University of Pisa · ITCasa Sollievo della Sofferenza · ITCharles University · CZGerman Cancer Research Center · DECzech Academy of Sciences, Institute of Experimental Medicine · CZHeidelberg University · DEInstitut Català d'Oncologia · ESIstituti di Ricovero e Cura a Carattere Scientifico · ITLithuanian University of Health Sciences · LT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGenetics plays an important role in the susceptibility to sporadic colorectal cancer (CRC). In the last 10 years genome-wide association studies (GWAS) have identified over 40 independent low penetrance polymorphic variants. However, these loci only explain around 1‑4% of CRC heritability, highlighting the dire need of identifying novel risk loci. In this study, we focused our attention on the genetic variability of the TAS2R16 gene, encoding for one of the bitter taste receptors that selectively binds to salicin, a natural antipyretic that resembles aspirin. Given the importance of inflammation in CRC, we tested whether polymorphic variants in this gene could affect the risk of developing this neoplasia hypothesizing a role of TAS2R16 in modulating chronic inflammation within the gut.

methodsWe performed an association study using 6 tagging SNPs, (rs860170, rs978739, rs1357949, rs1525489, rs6466849, rs10268496) that cover all TAS2R16 genetic variability. The study was carried out on 1902 CRC cases and 1532 control individuals from four European countries.

resultsWe did not find any statistically significant association between risk of developing CRC and selected SNPs. However, after stratification by histology (colon vs. rectum) we found that rs1525489 was associated with increased risk of rectal cancer with a (P

conclusionsOur data suggest that polymorphisms within TAS2R16 gene do not have a strong influence on colon cancer susceptibility, but a possible role in rectal cancer should be further evaluated in larger cohorts.

Indexed as

Genetic Predisposition to DiseasePolymorphism, Single NucleotideAgedCase-Control StudiesColonic NeoplasmsCzech RepublicFemaleGenetic Association StudiesHumansItalyLithuaniaMaleMiddle AgedReceptors, G-Protein-CoupledRectal NeoplasmsSpainReceptors, G-Protein-CoupledTaste Receptors, Type 2Cancer riskColon cancerColorectal cancerGenetic association studyPolymorphismsRectal cancerTAS2R16Taste receptors

Identifiers

PMID28915899
PMCPMC5603047
OpenAlexW2755722428

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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.