Evidence map›Paper›PMID 30155999›Full record

ArticleCancer medicine2018

SNP interactions of PGC with its neighbor lncRNAs enhance the susceptibility to gastric cancer/atrophic gastritis and influence the expression of involved molecules.

Zhi Lv, Liping Sun, Qian Xu, Yuehua Gong, Jingjing Jing, Nannan Dong, Chengzhong Xing, Yuan Yuan

Open access · goldAbstract read
In one paragraph

Article in Cancer medicine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.6field-weighted citation impact, top 37% 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

7 citing papers in PubMed, 8 citations in OpenAlex.

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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 at 1 institution in 1 country.

Zhi LvTumor Etiology and Screening Department of Cancer Institute and General Surgery, China Medical University First Hospital, Shenyang, China.
Liping SunTumor Etiology and Screening Department of Cancer Institute and General Surgery, China Medical University First Hospital, Shenyang, China.
Qian XuTumor Etiology and Screening Department of Cancer Institute and General Surgery, China Medical University First Hospital, Shenyang, China.
Yuehua GongTumor Etiology and Screening Department of Cancer Institute and General Surgery, China Medical University First Hospital, Shenyang, China.
Jingjing JingTumor Etiology and Screening Department of Cancer Institute and General Surgery, China Medical University First Hospital, Shenyang, China.
Nannan DongTumor Etiology and Screening Department of Cancer Institute and General Surgery, China Medical University First Hospital, Shenyang, China.
Chengzhong XingTumor Etiology and Screening Department of Cancer Institute and General Surgery, China Medical University First Hospital, Shenyang, China.ORCID 0000-0001-6463-019X
Yuan YuanTumor Etiology and Screening Department of Cancer Institute and General Surgery, China Medical University First Hospital, Shenyang, China.ORCID 0000-0002-7394-9036
Liaoning Cancer Hospital & Institute · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Multidimensional interactions of multiple factors are more important in promoting cancer initiation. Gene-gene interactions between protein-coding genes have been paid great attention, while rare studies refer to the interactions between encoding and noncoding genes. Our research group previously found encoding gene PGC polymorphisms could affect the susceptibility to atrophic gastritis (AG) and gastric cancer (GC). Interestingly, several SNPs in long noncoding RNA (lncRNA) genes, just adjacent to PGC, were found to be associated with AG risk and GC prognosis afterward. This study aims to explore the SNP interactions between PGC and its neighbor lncRNAs on the risk of AG and GC. Genotyping for seven PGC SNPs and seven lncRNA SNPs was conducted using Sequenom MassARRAY platform in a total of 2228 northern Chinese subjects, including 536 GC cases, 810 AG cases, and 882 controls. We found 15 pairwise PGC-lncRNAs SNPs had interactions: Five pairs were associated with AG risk, and ten pairs were associated with GC risk. Moreover, two GC-related interactions PGC rs6939861 with lnc-C6orf-132-1 rs7749023 and rs7747696 survived the Bonferroni correction (P

Indexed as

Polymorphism, Single NucleotideAlcohol DrinkingCase-Control StudiesChinaEpistasis, GeneticFemaleGastritis, AtrophicGenetic Predisposition to DiseaseHelicobacter InfectionsHumansMalePepsinogen CRNA, Long NoncodingSmokingStomach NeoplasmsPepsinogen CPGC protein, humanRNA, Long Noncodingatrophic gastritisgastric cancerLncRNAPGCpolymorphismsusceptibility

Identifiers

PMID30155999
PMCPMC6198214
OpenAlexW2889072868

What OpenQuestion holds

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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.