Evidence map›Paper›PMID 25347573›Full record

ArticlePloS one2014

Follistatin is a novel biomarker for lung adenocarcinoma in humans.

Fangfang Chen, Ping Ren, Ye Feng, Haiyan Liu, Yang Sun, Zhonghui Liu, Jingyan Ge, Xueling Cui

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.9field-weighted citation impact, top 28% 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, 19 citations in OpenAlex.

  1. Review
  2. Article
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  7. Developing a deeper insight into reproductive biomarkers.Clinical and experimental reproductive medicine · 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

8 authors at 4 institutions in 1 country.

Fangfang ChenDepartment of Gastrointestinal Surgery, China-Japan Union Hospital, Jilin University, Changchun, China.
Ping RenDepartment of Thoracic Surgery, First Hospital of Jilin University, Changchun, China.
Ye FengDepartment of Gastrointestinal Surgery, China-Japan Union Hospital, Jilin University, Changchun, China.
Haiyan LiuDepartment of Immunology, College of Basic Medical Sciences, Jilin University, Changchun, China.
Yang SunDepartment of Immunology, College of Basic Medical Sciences, Jilin University, Changchun, China.
Zhonghui LiuDepartment of Immunology, College of Basic Medical Sciences, Jilin University, Changchun, China.
Jingyan GeDepartment of Immunology, College of Basic Medical Sciences, Jilin University, Changchun, China.
Xueling CuiDepartment of Immunology, College of Basic Medical Sciences, Jilin University, Changchun, China.
Jilin Medical University · CNJilin University · CNFirst Hospital of Jilin University · CNUnion Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundFollistatin (FST), a single chain glycoprotein, is originally isolated from follicular fluid of ovary. Previous studies have revealed that serum FST served as a biomarker for pregnancy and ovarian mucinous tumor. However, whether FST can serve as a biomarker for diagnosis in lung adenocarcinoma of humans remains unclear. METHODS AND

resultsThe study population consisted of 80 patients with lung adenocarcinoma, 40 patients with ovarian adenocarcinoma and 80 healthy subjects. Serum FST levels in patients and healthy subjects were measured using ELISA. The results showed that the positive ratio of serum FST levels was 51.3% (41/80), which was comparable to the sensitivity of FST in 40 patients with ovarian adenocarcinoma (60%, 24/40) using the 95th confidence interval for the healthy subject group as the cut-off value. FST expressions in lung adenocarcinoma were examined by immunohistochemical staining, we found that lung adenocarcinoma could produce FST and there was positive correlation between the level of FST expression and the differential degree of lung adenocarcinoma. Furthermore, the results showed that primary cultured lung adenocarcinoma cells could secrete FST, while cells derived from non-tumor lung tissues almost did not produce FST. In addition, the results of CCK8 assay and flow cytometry showed that using anti-FST monoclonal antibody to neutralize endogenous FST significantly augmented activin A-induced lung adenocarcinoma cells apoptosis.

conclusionsThese data indicate that lung adenocarcinoma cells can secret FST into serum, which may be beneficial to the survival of adenocarcinoma cells by neutralizing activin A action. Thus, FST can serve as a promising biomarker for diagnosis of lung adenocarcinoma and a useful biotherapy target for lung adenocarcinoma.

Indexed as

AdenocarcinomaAdultAgedBiomarkers, TumorCase-Control StudiesFemaleFollistatinHumansLung NeoplasmsMaleMiddle AgedBiomarkers, TumorFollistatin

Identifiers

PMID25347573
PMCPMC4210220
OpenAlexW2033661404

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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.