Evidence map›Paper›PMID 26165253›Full record

SynthesisScientific reports2015

Tumour Necrosis Factor-α Gene Polymorphism Is Associated with Metastasis in Patients with Triple Negative Breast Cancer.

Hui-Hui Li, Hui Zhu, Li-Sheng Liu, Yong Huang, Jun Guo, Jie Li, Xin-Ping Sun, Chun-Xiao Chang, Zhe-Hai Wang, Kan Zhai

Open access · goldAbstract readMeta-Analysis
In one paragraph

Synthesis in Scientific reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 2 pooled it
1.6field-weighted citation impact, top 15% 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

19 citing papers in PubMed, 2 syntheses or guidelines pooled it, 26 citations in OpenAlex.

  1. Pooled it
  2. Genetic association betweenOncotarget · 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

10 authors at 4 institutions in 1 country.

Hui-Hui LiDepartment of Medical Oncology, Shandong Cancer Hospital and Institute, Jinan, Shandong 250117, China.
Hui ZhuDepartment of Radiation Oncology, Shandong Cancer Hospital and Institute, Jinan, Shandong 250117, China.
Li-Sheng LiuDepartment of Clinical Laboratory, Shandong Cancer Hospital and Institute, Jinan, Shandong 250117, China.
Yong HuangDepartment of Radiology, Shandong Cancer Hospital and Institute, Jinan, Shandong 250117, China.
Jun GuoDepartment of Medical Oncology, Shandong Cancer Hospital and Institute, Jinan, Shandong 250117, China.
Jie LiDepartment of General Surgery, Beijing Chao-Yang Hospital, Capital Medical University, Beijing 100020, China.
Xin-Ping SunDepartment of Clinical Laboratory, Shandong Provincial Hospital Affiliated to Shandong University, Jinan, Shandong 250117, China.
Chun-Xiao ChangDepartment of Medical Oncology, Shandong Cancer Hospital and Institute, Jinan, Shandong 250117, China.
Zhe-Hai WangDepartment of Medical Oncology, Shandong Cancer Hospital and Institute, Jinan, Shandong 250117, China.
Kan ZhaiMedical Research Center, Beijing Chao-Yang Hospital, Capital Medical University, Beijing 100020, China.
Shandong First Medical University · CNShandong Tumor Hospital · CNCapital Medical University · CNShandong University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tumour necrosis factor-α (TNF-α) is critical in the regulation of inflammation and tumour progression. TNF-α-308G > A is associated with constitutively elevated TNF-α expression. The purpose of this study was to assess the association between TNF-α-308G > A and breast cancer (BC) risk by subtype and the connection between genotypes and clinical features of BC. A total of 768 patients and 565 controls were enrolled in this study, and genotypes were detected using the TaqMan assay. No effect on susceptibility for any BC subtype was found for the TNF-α-308 polymorphism in our study or in the pooled meta-analysis. This polymorphism was shown to be associated with age at menarche in all BC and in progesterone receptor-negative BC. Interestingly, triple negative breast cancer (TNBC) patients with TNF-α-308A had an increased risk of distant tumour metastasis (OR = 3.80, 95% CI: 1.31-11.02, P = 0.009). Multi-regression analysis showed that TNF-α-308A was also a risk factor for distant tumour metastasis after adjustment for tumour size and lymph node metastasis status (OR = 6.26, 95% CI: 1.88-20.87, P = 0.003). These findings indicate that TNF-α might play a distinct role in the progression of TNBC, especially in distant tumour metastasis of TNBC.

Indexed as

AdultAllelesAsian PeopleDatabases, FactualFemaleGenotypeHumansMiddle AgedNeoplasm MetastasisOdds RatioPolymorphism, Single NucleotideRegression AnalysisTriple Negative Breast NeoplasmsTumor Necrosis Factor-alphaWhite PeopleTumor Necrosis Factor-alpha

Identifiers

PMID26165253
PMCPMC4499887
OpenAlexW2252399152

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.