Evidence map›Paper›PMID 26186548›Full record

ArticlePloS one2015

Associations between NBS1 Polymorphisms and Colorectal Cancer in Chinese Population.

Jing-Tao Li, Bao-Yuan Zhong, Hui-Hui Xu, Sheng-Yan Qiao, Gui Wang, Jing Huang, Hui-Zhen Fan, Hong-Chuan Zhao

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

6 citing papers in PubMed, 14 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. A non-synonymous polymorphism inOncoTargets and therapy · 2018
    Article
  6. 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

8 authors at 2 institutions in 1 country.

Jing-Tao LiDepartment of Gastroenterology, China-Japan Friendship Hospital, Beijing, China.
Bao-Yuan ZhongDepartment of general surgery, First Affiliated Hospital of Gannan Medical College, Ganzhou, China.
Hui-Hui XuInstitute of Clinical Medicine, China-Japan Friendship Hospital, Beijing, China.
Sheng-Yan QiaoInstitute of Clinical Medicine, China-Japan Friendship Hospital, Beijing, China.
Gui WangInstitute of Clinical Medicine, China-Japan Friendship Hospital, Beijing, China.
Jing HuangInstitute of Clinical Medicine, China-Japan Friendship Hospital, Beijing, China.
Hui-Zhen FanDepartment of Gastroenterology, The People's Hospital of Yichun City, Yichun, China.
Hong-Chuan ZhaoDepartment of Gastroenterology, China-Japan Friendship Hospital, Beijing, China.
China-Japan Friendship Hospital · CNFirst Affiliated Hospital of Gannan Medical University · CN

Funding

1/4 Alcohol Research Consortium in HIV-Administrative Core (ARCH-AC)U24AA020801 · NIAAA · JOHNS HOPKINS UNIVERSITY · PI CHANDER, GEETANJALI, MCCAUL, MARY E · 2011 to 2021
$3.5M
NIAAA NIH HHS U24 AA020801
6 · The paper itself

Abstract

As the central protein of the double strand breaks (DSB)-induced DNA repair pathway, NBS1 participates in detecting the DSBs and plays an essential role in maintaining genomic stability. Single nucleotide polymorphisms (SNPs) in NBS1 gene were commonly tested that associated with the susceptibility to multiple cancers, but the results remained controversial. Thus, we conducted two independent hospital-based case-control studies comprising 1,072 colorectal cancer patients and 1,263 controls to evaluate the association between four NBS1 SNPs and colorectal cancer risk. The result showed that rs2735383C/G polymorphism in the 3'-untranslated region (UTR) of NBS1 was significantly associated with risk of colorectal cancer using logistic regression (P<10(-4)). Furthermore, we observed that rs2735383CC genotype was associated with substantially increased risk of colorectal cancer (odds ratio=1.55, 95% confidence interval=1.27-1.94), compared with the rs2735383GC+GG genotypes. Further functional experiments demonstrated that the rs2735383C allele in the NBS1 disrupted the binding affinity of has-miR-509-5p to the NBS1 3'-UTR in colorectal cancer cells, affecting the NBS1 transcriptional activity and expression level. In conclusion, current evidence suggests that the rs2735383C/G polymorphism might contribute to the risk for colorectal cancer.

Indexed as

Genetic Association StudiesGenetic Predisposition to Disease3' Untranslated RegionsAdultAgedAged, 80 and overAsian PeopleBase SequenceCell Cycle ProteinsColorectal NeoplasmsGene Expression Regulation, NeoplasticGenes, ReporterHumansLuciferasesMiddle AgedMolecular Sequence Data3' Untranslated RegionsCell Cycle ProteinsLuciferasesNBN protein, humanNuclear ProteinsRNA, Messenger

Identifiers

PMID26186548
PMCPMC4505902
OpenAlexW1414832044

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.