Evidence map›Paper›PMID 27042104›Full record

ArticleOncoTargets and therapy2016

miR-429 functions as a tumor suppressor by targeting FSCN1 in gastric cancer cells.

Min Zhang, Bing-Bin Dong, Min Lu, Mei-Juan Zheng, He Chen, Jing-Zhen Ding, A-Man Xu, Yuan-Hong Xu

Open access · goldAbstract read
In one paragraph

Article in OncoTargets and therapy, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
3.3field-weighted citation impact, top 8% 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

42 citing papers in PubMed, 59 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Circ_0008035 Promotes Gastric Cancer Development via the miR-429/SMAD2 Cascade.The Turkish journal of gastroenterology : the official journal of Turkish Society of Gastroenterology · 2024
    Article
  6. Article
  7. PCAT19: the role in cancer pathogenesis and beyond.Frontiers in cell and developmental biology · 2024
    Review
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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 2 institutions in 2 countries.

Min ZhangClinical Laboratory, The First Affiliated Hospital of Anhui Medical University, Hefei, People's Republic of China.
Bing-Bin DongDepartment of General Surgery, The First Affiliated Hospital of Anhui Medical University, Hefei, People's Republic of China.
Min LuClinical Laboratory, The First Affiliated Hospital of Anhui Medical University, Hefei, People's Republic of China.
Mei-Juan ZhengClinical Laboratory, The First Affiliated Hospital of Anhui Medical University, Hefei, People's Republic of China.
He ChenClinical Laboratory, The First Affiliated Hospital of Anhui Medical University, Hefei, People's Republic of China.
Jing-Zhen DingDepartment of Cellular and Molecular Medicine, Howard Hughes Medical Institute, University of California at San Diego, La Jolla, CA, USA.
A-Man XuDepartment of General Surgery, The First Affiliated Hospital of Anhui Medical University, Hefei, People's Republic of China.
Yuan-Hong XuClinical Laboratory, The First Affiliated Hospital of Anhui Medical University, Hefei, People's Republic of China.
First Affiliated Hospital of Anhui Medical University · CNHoward Hughes Medical Institute · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

It has been previously reported that the deregulation of microRNAs in gastric cancer (GC) was correlated with the progression and prognosis. miR-429, a member of the miR-200 family, was previously shown to play an important role in human carcinomas. Our study shows that miR-429 is significantly downregulated in GC tissues compared with matched nontumor tissues. Overexpression of miR-429 in GC cells suppressed cell proliferation. Fascin-1 (FSCN1) was identified as one of the targets of miR-429 and knockdown of FSCN1 mimics the function of miR-429 overexpression. In conclusion, miR-429 acts as a tumor suppressor by targeting FSCN1, suggesting that miR-429 and FSCN1 can both be potential therapeutic targets of GC.

Indexed as

FSCN1gastric cancermiR-429proliferation

Identifiers

PMID27042104
PMCPMC4780435
OpenAlexW2289109832

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.