Evidence map›Paper›PMID 28036263›Full record

SynthesisOncotarget2017

Quantitative assessment of the diagnostic role of FHIT promoter methylation in non-small cell lung cancer.

Xin Geng, Weilin Pu, Yulong Tan, Zhouyi Lu, An Wang, Lixing Tan, Sidi Chen, Shicheng Guo, Jiucun Wang, Xiaofeng Chen

Open access · diamondAbstract readMeta-AnalysisReview
In one paragraph

Synthesis in Oncotarget, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
0.7field-weighted citation impact, top 25% 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

10 citing papers in PubMed, 1 synthesis or guideline pooled it, 14 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Tumor Suppressor 4.1N/Frontiers in genetics · 2022
    Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Association of FHIT expression andOncoTargets and therapy · 2017
    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

10 authors at 4 institutions in 1 country.

Xin GengDepartment of Cardiothoracic Surgery, Huashan Hospital, Fudan University, Shanghai 200032, China.
Weilin PuState Key Laboratory of Genetic Engineering, Collaborative Innovation Center for Genetics and Development, School of Life Sciences, Fudan University, Shanghai 200433, China.
Yulong TanDepartment of Cardiothoracic Surgery, Huashan Hospital, Fudan University, Shanghai 200032, China.
Zhouyi LuDepartment of Chest Surgery, Shanghai Pulmonary Hospital, Shanghai 200433, China.
An WangDepartment of Chest Surgery, Shanghai Pulmonary Hospital, Shanghai 200433, China.
Lixing TanState Key Laboratory of Genetic Engineering, Collaborative Innovation Center for Genetics and Development, School of Life Sciences, Fudan University, Shanghai 200433, China.
Sidi ChenState Key Laboratory of Genetic Engineering, Collaborative Innovation Center for Genetics and Development, School of Life Sciences, Fudan University, Shanghai 200433, China.
Shicheng GuoDepartment of Bioengineering, University of California at San Diego, La Jolla, CA 92093, USA.
Jiucun WangState Key Laboratory of Genetic Engineering, Collaborative Innovation Center for Genetics and Development, School of Life Sciences, Fudan University, Shanghai 200433, China.
Xiaofeng ChenDepartment of Cardiothoracic Surgery, Huashan Hospital, Fudan University, Shanghai 200032, China.
Fudan University · CNState Key Laboratory of Genetic EngineeringShanghai Pulmonary Hospital · CNHuashan Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Aberrant methylation of CpG islands acquired in promoter regions plays an important role in carcinogenesis. Accumulated evidence demonstrates FHIT gene promoter hyper-methylation is involved in non-small cell lung cancer (NSCLC). To test the diagnostic ability of FHIT methylation status on NSCLC, thirteen studies, including 2,119 samples were included in our meta-analysis. Simultaneously, four independent DNA methylation datasets from TCGA and GEO database were analyzed for validation. The pooled odds ratio of FHIT promoter methylation in cancer samples was 3.43 (95% CI: 1.85 to 6.36) compared with that in controls. In subgroup analysis, significant difference of FHIT gene promoter methylation status in NSCLC and controls was found in Asians but not in Caucasian population. In validation stage, 950 Caucasian samples, including 126 paired samples from TCGA, 568 cancer tissues and 256 normal controls from GEO database were analyzed, and all 8 CpG sites near the promoter region of FHIT gene were not significantly differentially methylated. Thus the diagnostic role of FHIT gene in the lung cancer may be relatively limited in the Caucasian population but useful in the Asians.

Indexed as

DNA MethylationPromoter Regions, GeneticAcid Anhydride HydrolasesAgedAsian PeopleBiomarkers, TumorBis(5'-adenosyl)triphosphataseCarcinoma, Non-Small-Cell LungCase-Control StudiesCpG IslandsDatabases, GeneticFemaleGenetic Predisposition to DiseaseHumansLung NeoplasmsMaleAcid Anhydride HydrolasesBiomarkers, TumorBis(5'-adenosyl)triphosphataseNeoplasm ProteinsdiagnosisDNA methylationFHITnon-small cell lung cancerNSCLC

Identifiers

PMID28036263
PMCPMC5351674
OpenAlexW2561885651

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.