Evidence map›Paper›PMID 27376157›Full record

ArticleJournal of gene therapy2016

MicroRNA-124 suppresses tumor cell proliferation and invasion by targeting CD164 signaling pathway in non-small cell lung cancer.

Jing Lin, Kai Xu, Jun Wei, Amy B Heimberger, Jack A Roth, Lin Ji

Open access · diamondAbstract read
In one paragraph

Article in Journal of gene therapy, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
3.1field-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

24 citing papers in PubMed, 35 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Observational
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article
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

6 authors at 1 institution in 1 country.

Jing LinDepartment of Thoracic & Cardiovascular Surgery, The University of Texas M.D. Anderson Cancer Center, Houston, TX, USA.
Kai XuDepartment of Thoracic & Cardiovascular Surgery, The University of Texas M.D. Anderson Cancer Center, Houston, TX, USA.
Jun WeiDepartment of Neurosurgery, The University of Texas M.D. Anderson Cancer Center, Houston, TX, USA.
Amy B HeimbergerDepartment of Neurosurgery, The University of Texas M.D. Anderson Cancer Center, Houston, TX, USA.
Jack A RothDepartment of Thoracic & Cardiovascular Surgery, The University of Texas M.D. Anderson Cancer Center, Houston, TX, USA.
Lin JiDepartment of Thoracic & Cardiovascular Surgery, The University of Texas M.D. Anderson Cancer Center, Houston, TX, USA.
The University of Texas MD Anderson Cancer Center · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
UNIVERSITY OF TEXAS--SPORE IN LUNG CANCERP50CA070907 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI GIBBONS, DON LYNN · 1996 to 2024
$57.4M
Epigenetic miRNA, SNP Signatures, and their Functions in Lung Cancer OutcomesR01CA176568 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI GU, JIAN, ROTH, JACK · 2014 to 2018
$2.5M
Tumor and PTK-Targeted Therapy by FUS1 and PTK inhibitorR01CA116322 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI JI, LIN · 2007 to 2010
$1.1M
NCI NIH HHS P30 CA016672NCI NIH HHS P50 CA070907NCI NIH HHS R01 CA116322NCI NIH HHS R01 CA176568
6 · The paper itself

Abstract

MicroRNAs play critical roles in regulating gene expression and various cellular processes in human cancer malignant progression. Down-regulated expression of miR-124 gene has been shown to be significantly associated with a poor prognosis in patients with non-small cell lung cancer (NSCLC) but its biological function and regulatory roles in lung cancer tumorigenesis are largely unknown. In this study, we aimed to determine effects of ectopic expression of miR-124 on tumor cell proliferation, invasion, and induction of apoptosis by DOTAP:Cholesterol nanoparticle-mediated gene transfer and identify its endogenous targets under physiological conditions in NSCLC cells. Overexpression of miR-124 significantly suppresses tumor cell proliferation, colony formation, migration, and induction of apoptosis in H322 and A549 cells. Two endogenous miR-124 targeting sites in the 3'UTR of CD164 mRNA are identified by a stem-loop-array reverse transcription PCR (SLA-RT-PCR) assay in H1299 cells under physiological condition. Ectopic expression of miR-124 induces CD164 mRNA cleavage and down-regulated its gene and protein expression. Our results suggest that miR-124 function as a tumor suppressor miRNA and suppress tumor proliferation and aggression by directly targeting oncogenic CD164 signaling pathway in NSCLC.

Identifiers

PMID27376157
PMCPMC4927004
OpenAlexW2467589961

What OpenQuestion holds

Textmetadata
LicenceTDM
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.