Evidence map›Paper›PMID 26102366›Full record

ArticlePloS one2015

MicroRNA-137 Contributes to Dampened Tumorigenesis in Human Gastric Cancer by Targeting AKT2.

Liping Wu, Jingtao Chen, Chunsheng Ding, Shutang Wei, Yanhong Zhu, Wenyi Yang, Xiaoyang Zhang, Xuejv Wei, Dazheng Han

RetractedOpen access · goldAbstract readRetracted Publication
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It has been retracted, and should not be counted. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.9field-weighted citation impact, top 16% 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

18 citing papers in PubMed, 40 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. MicroRNA-137 represses FBI-1 to inhibit proliferation and in vitro invasion and migration of hepatocellular carcinoma cells.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2016
    Article
  17. Article
  18. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 1 institution in 1 country.

Liping WuDepartment of Gastroenterology, First affiliated Hospital of Henan University, Kaifeng, Henan, China.
Jingtao ChenDepartment of Gastroenterology, First affiliated Hospital of Henan University, Kaifeng, Henan, China.
Chunsheng DingDepartment of Gastroenterology, First affiliated Hospital of Henan University, Kaifeng, Henan, China.
Shutang WeiDepartment of Gastroenterology, First affiliated Hospital of Henan University, Kaifeng, Henan, China.
Yanhong ZhuDepartment of Gastroenterology, First affiliated Hospital of Henan University, Kaifeng, Henan, China.
Wenyi YangDepartment of Gastroenterology, First affiliated Hospital of Henan University, Kaifeng, Henan, China.
Xiaoyang ZhangDepartment of Gastroenterology, First affiliated Hospital of Henan University, Kaifeng, Henan, China.
Xuejv WeiDepartment of Gastroenterology, First affiliated Hospital of Henan University, Kaifeng, Henan, China.
Dazheng HanDepartment of Gastroenterology, First affiliated Hospital of Henan University, Kaifeng, Henan, China.
First Affiliated Hospital of Henan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

MiRNAs play important roles in tumorigenesis. This study focused on exploring the effects and regulation mechanism of miRNA-137 on the biological behaviors of gastric cancer. Total RNA was extracted from tissues of 100 patients with gastric cancer and from four gastric cancer cell lines. Expression of miR-137 was detected by real-time PCR from 100 patients. The effects of miR-137 overexpression on gastric cancer cells' proliferation, apoptosis, migration and invasion ability were investigated in vitro and in vivo. The target gene of miR-137 was predicted by Targetscan on line software, screened by dual luciferase reporter gene assay and demonstrated by western blot. As a result, the expression of miR-137 was significant reduced in gastric cancer cell line HGC-27, HGC-803, SGC-7901 and MKN-45 as well as in gastric cancer tissues compared with GES-1 cell or matched adjacent non-neoplastic tissues (p<0.001). The re-introduction of miR-137 into gastric cancer cells was able to inhibit cell proliferation, migration and invasion. The in vivo experiments demonstrated that the miR-137 overexpression can reduce the gastric cancer cell proliferation and metastasis. Bioinformatic and western blot analysis indicated that the miR-137 acted as tumor suppressor roles on gastric cancer cells through targeting AKT2 and further affecting the Bad and GSK-3β. In conclusion, the miR-137 which is frequently down-regulated in gastric cancer is potentially involved in gastric cancer tumorigenesis and metastasis by regulating AKT2 related signal pathways.

Indexed as

AnimalsCarcinogenesisCell Line, TumorCell ProliferationDown-RegulationHeterograftsHumansMiceMice, Inbred BALB CMice, NudeMicroRNAsProto-Oncogene Proteins c-aktStomach NeoplasmsAKT2 protein, humanMicroRNAsMIRN137 microRNA, humanProto-Oncogene Proteins c-akt

Identifiers

PMID26102366
PMCPMC4477888
OpenAlexW2117059884

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.