Evidence map›Paper›PMID 28639733›Full record

ArticleCancer medicine2017

Genetic variants of cell cycle pathway genes predict disease-free survival of hepatocellular carcinoma.

Shun Liu, Tian-Bo Yang, Yue-Li Nan, An-Hua Li, Dong-Xiang Pan, Yang Xu, Shu Li, Ting Li, Xiao-Yun Zeng, Xiao-Qiang Qiu

Open access · goldAbstract read
In one paragraph

Article in Cancer medicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

11 citing papers in PubMed, 30 citations in OpenAlex.

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  2. Cancer biology & therapy · 2024
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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

10 authors at 4 institutions in 1 country.

Shun LiuDepartment of Epidemiology, School of Public Health, Guangxi Medical University, 22 Shuangyong Road, Nanning, Guangxi, 530021, China.ORCID http://orcid.org/0000-0002-1389-5929
Tian-Bo YangAffiliated Tumor Hospital of Guangxi Medical University, 71 Hedi Road, Nanning, Guangxi, 530021, China.
Yue-Li NanShenzhen Longhua Center for Chronic Diseases Prevention and Control, 118 Guanlan Road, Shenzhen, Guangdong, 518110, China.
An-Hua LiGuangXi Center for Disease Prevention and Control, 18 Jinzhou Road, Nanning, Guangxi, 530021, China.
Dong-Xiang PanGuangXi Center for Disease Prevention and Control, 18 Jinzhou Road, Nanning, Guangxi, 530021, China.
Yang XuDepartment of Epidemiology, School of Public Health, Guangxi Medical University, 22 Shuangyong Road, Nanning, Guangxi, 530021, China.
Shu LiDepartment of Epidemiology, School of Public Health, Guangxi Medical University, 22 Shuangyong Road, Nanning, Guangxi, 530021, China.
Ting LiMedical Scientific Research Centre, Guangxi Medical University, 22 Shuangyong Road, Nanning, Guangxi, 530021, China.
Xiao-Yun ZengDepartment of Epidemiology, School of Public Health, Guangxi Medical University, 22 Shuangyong Road, Nanning, Guangxi, 530021, China.
Xiao-Qiang QiuDepartment of Epidemiology, School of Public Health, Guangxi Medical University, 22 Shuangyong Road, Nanning, Guangxi, 530021, China.
Guangxi Medical University · CNGuangxi Center for Disease Prevention and Control · CNShenzhen Center for Disease Control and Prevention · CNTumor Hospital of Guangxi Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Disruption of the cell cycle pathway has previously been related to development of human cancers. However, associations between genetic variants of cell cycle pathway genes and prognosis of hepatocellular carcinoma (HCC) remain largely unknown. In this study, we evaluated the associations between 24 potential functional single nucleotide polymorphisms (SNPs) of 16 main cell cycle pathway genes and disease-free survival (DFS) of 271 HCC patients who had undergone radical surgery resection. We identified two SNPs, i.e., SMAD3 rs11556090 A>G and RBL2 rs3929G>C, that were independently predictive of DFS in an additive genetic model with false-positive report probability (FPRP) <0.2. The SMAD3 rs11556090G allele was associated with a poorer DFS, compared with the A allele [hazard ratio (HR) = 1.46, 95% confidential interval (95% CI) = 1.13-1.89, P = 0.004]; while the RBL2 rs3929 C allele was associated with a superior DFS, compared with the G allele (HR = 0.74, 95% CI = 0.57-0.96, P = 0.023). Additionally, patients with an increasing number of unfavorable genotypes (NUGs) of these loci had a significant shorter DFS (P

Indexed as

Genetic VariationAdultAgedAllelesCarcinoma, HepatocellularCase-Control StudiesCell CycleComorbidityFemaleFollow-Up StudiesGenetic Predisposition to DiseaseGenotypeHumansKaplan-Meier EstimateLiver NeoplasmsMaleCell cycle pathwayhepatocellular carcinomasingle-nucleotide polymorphismsurvival

Identifiers

PMID28639733
PMCPMC5504311
OpenAlexW2701354224

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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.