Evidence map›Paper›PMID 28693227›Full record

ArticleOncology letters2017

Polymorphisms of -800G/A and +915G/C in TGF-β1 gene and lung cancer susceptibility.

Qing-Guo Di, Bao-Hua Sun, Ming-Ming Jiang, Jun-Feng Du, Zhi-Tao Mai, Xin Zhang, Li-Rong Zhou, Yu-Min Chi, Jing Lv

Open access · diamondAbstract read
In one paragraph

Article in Oncology letters, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.1field-weighted citation impact, top 50% 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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Association of the TGF-beta1 polymorphism with primary open-angle glaucoma: a case-control study.Medical hypothesis, discovery & innovation ophthalmology journal · 2026
    Article
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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

9 authors at 1 institution in 1 country.

Qing-Guo DiDepartment of Respiration Medicine, Cangzhou Central Hospital, Cangzhou, Hebei 061000, P.R. China.
Bao-Hua SunDepartment of Respiration Medicine, Cangzhou Central Hospital, Cangzhou, Hebei 061000, P.R. China.
Ming-Ming JiangDepartment of Respiration Medicine, Cangzhou Central Hospital, Cangzhou, Hebei 061000, P.R. China.
Jun-Feng DuDepartment of Respiration Medicine, Cangzhou Central Hospital, Cangzhou, Hebei 061000, P.R. China.
Zhi-Tao MaiDepartment of Respiration Medicine, Cangzhou Central Hospital, Cangzhou, Hebei 061000, P.R. China.
Xin ZhangDepartment of Respiration Medicine, Cangzhou Central Hospital, Cangzhou, Hebei 061000, P.R. China.
Li-Rong ZhouDepartment of Respiration Medicine, Cangzhou Central Hospital, Cangzhou, Hebei 061000, P.R. China.
Yu-Min ChiDepartment of Respiration Medicine, Cangzhou Central Hospital, Cangzhou, Hebei 061000, P.R. China.
Jing LvDepartment of Respiration Medicine, Cangzhou Central Hospital, Cangzhou, Hebei 061000, P.R. China.
Cangzhou Central Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We studied the relationship between the polymorphisms of -800G/A and +915G/C in transforming growth factor-β1 (TGF-β1) gene and lung cancer susceptibility. The sequence-specific primer polymerase chain reaction (PCR-SSP) technique was used to test 156 non-small cell lung cancer (NSCLC) patients that were selected as the observation group and 156 patients with pneumonia and tuberculosis that were selected as the control group (age and gender 1:1 proximal matching principle) and the polymorphisms of the first exon -800G/A and +915G/C TGF-β1 genes. The expression of TGF-β1 levels in peripheral blood was detected using ELISA. The proportion of -800G/A gene AA subtype and A allelic gene in the observation group was significantly higher than that in the control group, while the proportion of +915G/C gene CC subtype and C allelic gene was also significantly higher than that in the control group (P<0.05). The cancer risk [odds ratio (OR)] of patients with A allelic gene in -800G/A gene was 4.8 (95% CI=2.563-6.537, P<0.05), while the cancer risk (OR) of patients with C allelic gene in +915G/C gene was 4.7 (95% CI=2.317-5.864, P<0.05). The serum TGF-β1 expression levels of -800G/A gene AA subtype in the observation group was significantly higher than the GG type, GA type and the control group, while the TGF-β1 level of +915G/C gene CC subtype was significantly higher than the GG type, GC type and the control group (P<0.05). Therefore, the polymorphisms of -800G/A and +915G/C in TGF-β1 gene are closely related to the lung cancer susceptibility.

Indexed as

gene polymorphismlung cancer susceptibilitytransforming growth factor-β1

Identifiers

PMID28693227
PMCPMC5494756
OpenAlexW2615933263

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.