Evidence map›Paper›PMID 26302683›Full record

ArticleJournal of clinical laboratory analysis2016

Genotype GG of rs895819 Functional Polymorphism Within miR-27a Might Increase Genetic Susceptibility to Colorectal Cancer in Han Chinese Population.

Yu Jiang, Dong-Hong Lin, Jian-Ping Xu, Wen-Xu Chen, Shu-Jian Zheng, Lin Song

Abstract read
In one paragraph

Article in Journal of clinical laboratory analysis, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 2 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

14 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. mirSNPs as Potential Colorectal Cancer Biomarkers: A Systematic Review.International journal of molecular sciences · 2024
    Pooled it
  2. Pooled it
  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. MethylatedOncotarget · 2017
    Article
  12. Article
  13. Genetic variationOncoTargets and therapy · 2016
    Article
  14. MicroRNAs and Cancer Racial Disparities.Wiley interdisciplinary reviews. RNA
    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

6 authors.

Yu JiangDepartment of Clinical Laboratory, Fuzhou Second Hospital, Xiamen University, Fuzhou, Fujian, P.R. China.
Dong-Hong LinDepartment of Clinical Laboratory Medicine, Fujian Medical University, Taijiang, Fuzhou, P.R. China.
Jian-Ping XuDepartment of Clinical Laboratory Medicine, Fujian Medical University, Taijiang, Fuzhou, P.R. China.
Wen-Xu ChenDepartment of Clinical Laboratory, Fuzhou Second Hospital, Xiamen University, Fuzhou, Fujian, P.R. China.
Shu-Jian ZhengOncological Surgery, Fuzhou Second Hospital, Xiamen University, Fuzhou, Fujian, P.R. China.
Lin SongOncological Surgery, Fuzhou Second Hospital, Xiamen University, Fuzhou, Fujian, P.R. China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMicroRNA-27a (miR-27a) is supposed to be an oncogene in various types of cancers, and genetic variation of miR-27a might result in aberrant expression and abnormal second structure of mature-miR-27a, contributing to elevated genetic risk and poor prognosis for colorectal cancer (CRC).

methodsIn order to explore the possible association between rs895819 within miR-27a and CRC in Han Chinese population, we investigated the genotype distributions of rs895819 in 508 CRC cases and 562 healthy check-up controls using TaqMan genotype discrimination system, and analyzed the possible association between them. Odds ratio (OR) and 95% confidential interval (95% CI) were used to assess the strength between allele and genotype of the locus and risk of CRC.

resultsIn our study, we found that genotype GG of rs895819 was significantly associated with an increased risk for CRC (17.1% vs. 11.6%, adjusted OR = 1.546, 95% CI = 1.070-2.236), and allele A carrier (AA/AG) was significantly associated with a decreased risk for CRC (82.9% vs. 89.4%, adjusted OR = 0.63, 95% CI = 0.446-0.893). In addition, a significant association was observed between genotype GG and larger tumor size (>5 cm; P < 0.001), and allele G was significantly associated with higher pathological stage (TNM-III) (P = 0.008).

conclusionThese results indicated that miR-27a might be involved in the development and progression of CRC, genotype GG within rs895819 might be a genetic susceptible factor for CRC. Further multicentral, large sample size, and well-designed epidemiological study as well as functional study are warrant to verify our findings.

Indexed as

Genetic Predisposition to DiseaseAllelesAsian PeopleCase-Control StudiesColorectal NeoplasmsEthnicityFemaleHumansMaleMicroRNAsMiddle AgedPolymorphism, Single NucleotideMicroRNAsMIRN27 microRNA, humancolorectal cancerpolymorphismrs895819

Identifiers

PMID26302683
PMCPMC6806710

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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.