Evidence map›Paper›PMID 27057629›Full record

ArticleOncotarget2016

Protein profiling of alpha-fetoprotein producing gastric adenocarcinoma.

Liang He, Fei Ye, Linlin Qu, Daguang Wang, Miao Cui, Chengguo Wei, Yanpeng Xing, Peng Lee, Jian Suo, David Y Zhang

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 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

12 citing papers in PubMed, 1 synthesis or guideline pooled it, 20 citations in OpenAlex.

  1. Pooled it
  2. Review
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  12. Advances in the Clinical Application of High-throughput Proteomics.Exploratory research and hypothesis in medicine
    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 2 countries.

Liang HeDepartment of Gastrointestinal Surgery, First Hospital of Jilin University, Changchun, China.
Fei YeDepartment of Pathology, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Linlin QuDepartment of Clinical Laboratory, First Hospital of Jilin University, Changchun, China.
Daguang WangDepartment of Gastrointestinal Surgery, First Hospital of Jilin University, Changchun, China.
Miao CuiDepartment of Pathology, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Chengguo WeiDepartment of Nephrology, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Yanpeng XingDepartment of Gastrointestinal Surgery, First Hospital of Jilin University, Changchun, China.
Peng LeeDepartment of Pathology, New York University School of Medicine, New York, NY, USA.
Jian SuoDepartment of Gastrointestinal Surgery, First Hospital of Jilin University, Changchun, China.
David Y ZhangDepartment of Pathology, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
First Hospital of Jilin University · CNIcahn School of Medicine at Mount Sinai · USJilin University · CNNew York University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Alpha-fetoprotein (AFP) producing gastric adenocarcinoma is considered as a rare subtype of gastric adenocarcinoma. Compared with AFP non-producing gastric adenocarcinoma, our study and other previous studies showed that AFP producing gastric adenocarcinoma is more aggressive and prone to liver metastasis. Using the Protein Pathway Array, 11 of out of 286 proteins tested were found to be differentially expressed between AFP producing (n=32) and AFP non-producing (n=45) gastric adenocarcinoma tissues. In addition, the high level expression of XIAP and IGF-Irβ in gastric adenocarcinoma tissues was independent factors for poor prognosis in AFP producing gastric adenocarcinoma patients. A risk model based on the XIAP and IGF-Irβ expression levels can separate AFP producing gastric adenocarcinoma patients into 2 subgroups and each subgroup had a distinct set of signaling pathways involved. In conclusion, AFP producing gastric adenocarcinoma is a heterogeneous cancer with different clinical outcomes, biological behaviors and underlying molecular alterations.

Indexed as

AdenocarcinomaAdultAgedalpha-FetoproteinsDisease-Free SurvivalFemaleHumansKaplan-Meier EstimateMaleMiddle AgedPrognosisProportional Hazards ModelsProteomeProteomicsStomach NeoplasmsAFP protein, humanalpha-FetoproteinsProteomeAFPgastric cancersignaling pathwayssurvival analysis

Identifiers

PMID27057629
PMCPMC5053738
OpenAlexW2341684562

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.