Evidence map›Paper›PMID 26880585›Full record

ArticleTumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine2016

Association of toll-like receptor 2 ∆22 and risk for gastric cancer considering main effects and interactions with smoking: a matched case-control study from Mizoram, India.

Debdutta Mukherjee, Kangjam Rekha Devi, Manab Deka, Mridul Malakar, Tanvir Kaur, Debajit Barua, Jagadish Mahanta, Kanwar Narain

Abstract read
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In one paragraph

Article in Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

3 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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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

8 authors.

Debdutta MukherjeeRegional Medical Research Centre, N.E. Region (Indian Council of Medical Research), Post Box #105, Dibrugarh, 786 001, Assam, India.
Kangjam Rekha DeviRegional Medical Research Centre, N.E. Region (Indian Council of Medical Research), Post Box #105, Dibrugarh, 786 001, Assam, India.
Manab DekaDepartment of Biological Sciences, Gauhati University, Guwahati, Assam, India.
Mridul MalakarRegional Medical Research Centre, N.E. Region (Indian Council of Medical Research), Post Box #105, Dibrugarh, 786 001, Assam, India.
Tanvir KaurIndian Council of Medical Research, New Delhi, India.
Debajit BaruaAizawl Endoscopy Centre, Aizawl, Mizoram, India.
Jagadish MahantaRegional Medical Research Centre, N.E. Region (Indian Council of Medical Research), Post Box #105, Dibrugarh, 786 001, Assam, India.
Kanwar NarainRegional Medical Research Centre, N.E. Region (Indian Council of Medical Research), Post Box #105, Dibrugarh, 786 001, Assam, India. kanwar_narain@hotmail.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Toll-like receptors (TLRs) are evolutionary conserved cell surface receptors of the innate immune system. Smoking has significant immunological effects which are mediated via TLRs on various receptor-mediated innate response pathways. Polymorphisms of TLR genes are associated with susceptibility toward various malignancies. The present study was undertaken to examine the association between TLR2 ∆22 and gastric cancer. In this study, we also investigated the interaction between TLR2 ∆22 and smoking. A total of 133 histologically confirmed gastric cancer cases and 266 age-sex-matched controls were selected for this study. TLR2 ∆22 genotypes were determined by allele-specific polymerase chain reaction (PCR). Binary conditional logistic regression analysis was used to find the association of TLR2 ∆22 with risk of gastric cancer. Logistic regression using hierarchically well-formulated models was used for interaction analysis between smoking and TLR2 ∆22. Persons having TLR2 ∆22 heterozygous genotype had two times increased risk of gastric cancer in multivariate logistic regression model. The interaction analysis using hierarchical logistic regression models between smoking and TLR2 ∆22 by calculating separate X (2) for interaction model and only main effect model, the difference of X (2) 57.68-47.70 = 9.98 and degrees of freedom (df) 5-3 = 2, revealed significant (α = 0.05, df = 2) omnibus interaction. Our present study revealed TLR2 ∆22 to be significantly and independently associated with gastric cancer risk in Mizoram, and there is also evidence of significant interaction between smoking and TLR2 ∆22 with risk of gastric cancer.

Indexed as

AdultAgedCase-Control StudiesFemaleGenetic Predisposition to DiseaseGenotypeHumansIndiaMaleMiddle AgedPolymerase Chain ReactionPolymorphism, Single NucleotideRisk FactorsSmokingStomach NeoplasmsToll-Like Receptor 2TLR2 protein, humanToll-Like Receptor 2Gastric cancerInteraction analysisLogistic regressionSmokingTLR2 ∆22

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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.