Evidence map›Paper›PMID 26131234›Full record

ArticleInternational journal of clinical and experimental medicine2015

Association of interleukin-6 polymorphisms with susceptibility to hepatocellular carcinoma.

Xiaohuan Zheng, Cuiping Han, Rong Shan, Haitao Zhang, Zhaomin Zheng, Yuanshui Liu, Aiguang Wang

Open access · greenAbstract read
In one paragraph

Article in International journal of clinical and experimental medicine, 2015. 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
1.3field-weighted citation impact, top 19% 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

14 citing papers in PubMed, 2 syntheses or guidelines pooled it, 18 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Prognostic Impact of IL6 Genetic Variants in Patients with Metastatic Colorectal Cancer Treated with Bevacizumab-Based Chemotherapy.Clinical cancer research : an official journal of the American Association for Cancer Research · 2016
    Trial
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  9. Takayasu arteritis risk locus inAnnals of the rheumatic diseases · 2019
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  12. Determination ofOncotarget · 2017
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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

7 authors at 1 institution in 1 country.

Xiaohuan ZhengDepartment of Oncology, Qianfoshan Hospital Affiliated to Shandong University Jinan, Shandong, China.
Cuiping HanDepartment of Oncology, Qianfoshan Hospital Affiliated to Shandong University Jinan, Shandong, China.
Rong ShanDepartment of Oncology, Qianfoshan Hospital Affiliated to Shandong University Jinan, Shandong, China ; Department of Function, Jinan Infectious Disease Hospital Jinan, Shandong, China.
Haitao ZhangDepartment of Oncology, Qianfoshan Hospital Affiliated to Shandong University Jinan, Shandong, China.
Zhaomin ZhengDepartment of Oncology, Qianfoshan Hospital Affiliated to Shandong University Jinan, Shandong, China.
Yuanshui LiuDepartment of Oncology, Qianfoshan Hospital Affiliated to Shandong University Jinan, Shandong, China.
Aiguang WangDepartment of Oncology, Qianfoshan Hospital Affiliated to Shandong University Jinan, Shandong, China.
Shandong Provincial QianFoShan Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

targetOur study was to investigate the effects of interleukin-6 (IL-6) polymorphisms (rs2069837 and rs17147230) on the risk for hepatocellular carcinoma (HCC).

methodsA total of 226 HCC cases and 220 healthy controls were admitted into the study and genomic DNA was extracted from the peripheral blood. The genotyping was conducted by the method of polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP). Odds ratio (OR) and 95% confidence interval (CI) were used to evaluate the relationship of IL-6 rs2069837 and rs17147230 polymorphisms with HCC susceptibility.

resultsThe frequency of GG genotype of rs2069837 was higher in HCC patients, compared with controls (P < 0.05). Moreover, the results indicated that GG genotype was related with increased risk for HCC (OR = 2.303, 95% CI = 1.056-5.025). Similarly, the risk for G allele carriers was higher than that of A allele (OR = 1.392, 95% CI = 1.046-1.852). For rs17147230, TT genotype showed strong effect on HCC susceptibility (OR = 2.089, 95% CI = 1.135-3.845) and T allele appeared to be a risk factor for HCC (OR = 1.326, 95% CI = 1.010-1.740). Further analysis showed that G-T haplotype was associated with increased risk for HCC (OR = 3.125, 95% CI = 1.845-5.294, P = 0.000).

conclusionIL-6 rs2069837 as well as rs17147230 were associated with HCC susceptibility. In addition, G-T haplotype also served as a genetic-susceptibility factor for HCC.

Indexed as

hepatocellular carcinomaInterleukin-6polymorphisms

Identifiers

PMID26131234
PMCPMC4483998
OpenAlexW832904340

What OpenQuestion holds

Textmetadata
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.