Evidence map›Paper›PMID 29845203›Full record

ArticleMolecular medicine reports2018

Fibrinogen‑like‑protein 1 promotes the invasion and metastasis of gastric cancer and is associated with poor prognosis.

Yang Zhang, Hui-Xia Qiao, Yong-Tao Zhou, Liang Hong, Ju-Hui Chen

Open access · hybridAbstract read
In one paragraph

Article in Molecular medicine reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed, 1 pooled it
2.2field-weighted citation impact, top 9% 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

55 citing papers in PubMed, 1 synthesis or guideline pooled it, 73 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. GATA1 knockdown enhances CD8Journal of molecular histology · 2026
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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

5 authors at 3 institutions in 1 country.

Yang ZhangDepartment of Gastroenterology, Zhengzhou Central Hospital Affiliated to Zhengzhou University, Zhengzhou, Henan 450007, P.R. China.
Hui-Xia QiaoDepartment of Spleen and Stomach, Xi'an Traditional Chinese Medicine Hospital, Xi'an, Shanxi 710021, P.R. China.
Yong-Tao ZhouDepartment of Abdominal Radiotherapy, Fujian Province Cancer Hospital, Fuzhou, Fujian 350014, P.R. China.
Liang HongDepartment of Pathology, Fujian Province Cancer Hospital, Fuzhou, Fujian 350014, P.R. China.
Ju-Hui ChenDepartment of Abdominal Radiotherapy, Fujian Province Cancer Hospital, Fuzhou, Fujian 350014, P.R. China.
Fujian Provincial Cancer Hospital · CNShaanxi Provincial Hospital of Traditional Chinese Medicine · CNZhengzhou Central Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The protective role of fibrinogen‑like‑protein 1 (FGL1) in liver injury has been reported previously. However, there are few studies on FGL1 expression in gastric cancer (GC) tissues, and the role of FGL1 in GC remains unclear. The aim of the present study was to investigate the correlation between FGL1 expression and prognosis in GC patients. Data was downloaded from The Cancer Genome Atlas database, and 50 pairs of GC tissues and the corresponding non‑tumor tissues were collected between 2008 to 2011. Furthermore, FGL1 expression was silenced in order to explore its role in SGC‑7901 cell proliferation, invasion and migration using Cell Counting Kit‑8, wound healing, Transwell invasion and migration assays, respectively. Finally, whether FGL1 is involved in epithelial‑mesenchymal transition (EMT) regulation in SGC‑7901 cells was determined by western blotting. The results revealed that FGL1 expression was upregulated in GC tissues, and the overall survival time of GC patients with high FGL1 expression levels was markedly shorter than that of GC patients with low FGL1 expression levels (P=0.005). In addition, silencing FGL1 significantly inhibited SGC‑7901 cell proliferation, invasion and migration in vitro. Finally, western blot analyses indicated that knockdown of FGL1 markedly increased E‑cadherin expression levels (P<0.01), and significantly decreased N‑cadherin (P<0.01) and vimentin expression levels (P<0.01), thereby suggesting that FGL1 may promote EMT. These results indicated that FGL1 has the potential to be a predictor in GC patients as well as a target for the treatment of GC.

Indexed as

Gene Expression Regulation, NeoplasticAdenocarcinomaAgedAntigens, CDAtlases as TopicCadherinsCell Line, TumorCell MovementCell ProliferationDatabases, GeneticEpithelial-Mesenchymal TransitionFibrinogenHumansLymphatic MetastasisMaleMiddle AgedAntigens, CDCadherinsCDH1 protein, humanCDH2 protein, humanFGL1 protein, humanFibrinogenNeoplasm ProteinsRNA, Small InterferingVimentin

Identifiers

PMID29845203
PMCPMC6072172
OpenAlexW2805629425

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.