Evidence map›Paper›PMID 27684953›Full record

ArticlePloS one

Quantitative Proteomic Profiling the Molecular Signatures of Annexin A5 in Lung Squamous Carcinoma Cells.

Bing Sun, Yuxin Bai, Liyuan Zhang, Linlin Gong, Xiaoyu Qi, Huizhen Li, Faming Wang, Xinming Chi, Yulin Jiang, Shujuan Shao

Open access · goldAbstract read
In one paragraph

Article in PloS one. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
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

7 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
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  3. Frontiers in physiology · 2021
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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 2 institutions in 1 country.

Bing SunDepartment of Thoracic Surgery, The First Affiliated Hospital of Dalian Medical University, Dalian, 116011, Liaoning, China.
Yuxin BaiKey Laboratory for Proteomics of Liaoning Province, Dalian Medical University, Lvshun South Road No 9, Dalian, 116044, Liaoning, China.
Liyuan ZhangKey Laboratory for Proteomics of Liaoning Province, Dalian Medical University, Lvshun South Road No 9, Dalian, 116044, Liaoning, China.
Linlin GongKey Laboratory for Proteomics of Liaoning Province, Dalian Medical University, Lvshun South Road No 9, Dalian, 116044, Liaoning, China.
Xiaoyu QiKey Laboratory for Proteomics of Liaoning Province, Dalian Medical University, Lvshun South Road No 9, Dalian, 116044, Liaoning, China.
Huizhen LiKey Laboratory for Proteomics of Liaoning Province, Dalian Medical University, Lvshun South Road No 9, Dalian, 116044, Liaoning, China.
Faming WangKey Laboratory for Proteomics of Liaoning Province, Dalian Medical University, Lvshun South Road No 9, Dalian, 116044, Liaoning, China.
Xinming ChiKey Laboratory for Proteomics of Liaoning Province, Dalian Medical University, Lvshun South Road No 9, Dalian, 116044, Liaoning, China.
Yulin JiangKey Laboratory for Proteomics of Liaoning Province, Dalian Medical University, Lvshun South Road No 9, Dalian, 116044, Liaoning, China.
Shujuan ShaoKey Laboratory for Proteomics of Liaoning Province, Dalian Medical University, Lvshun South Road No 9, Dalian, 116044, Liaoning, China.
Dalian Medical University · CNFirst Affiliated Hospital of Dalian Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lung cancer remains the leading cancer killer around the world. It's crucial to identify newer mechanism-based targets to effectively manage lung cancer. Annexin A5 (ANXA5) is a protein kinase C inhibitory protein and calcium dependent phospholipid-binding protein, which may act as an endogenous regulator of various pathophysiological processes. However, its molecular mechanism in lung cancer remains poorly understood. This study was designed to determine the mechanism of ANXA5 in lung cancer with a hope to obtain useful information to provide a new therapeutic target. We used a stable isotope dimethyl labeling based quantitative proteomic method to identify differentially expressed proteins in NSCLC cell lines after ANXA5 transfection. Out of 314 proteins, we identified 26 and 44 proteins that were down- and up-regulated upon ANXA5 modulation, respectively. The IPA analysis revealed that glycolysis and gluconeogenesis were the predominant pathways modulated by ANXA5. Multiple central nodes, namely HSPA5, FN1, PDIA6, ENO1, ALDOA, JUP and KRT6A appeared to occupy regulatory nodes in the protein-protein networks upon ANXA5 modulation. Taken together, ANXA5 appears to have pleotropic effects, as it modulates multiple key signaling pathways, supporting the potential usefulness of ANXA5 as a potential target in lung cancer. This study might provide a new insight into the mechanism of ANXA5 in lung cancer.

Identifiers

PMID27684953
PMCPMC5042544
OpenAlexW2526458609

What OpenQuestion holds

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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.