Evidence map›Paper›PMID 27669434›Full record

ArticleOncogene2017

Targeting KRas-dependent tumour growth, circulating tumour cells and metastasis in vivo by clinically significant miR-193a-3p.

E G Seviour, V Sehgal, D Mishra, R Rupaimoole, C Rodriguez-Aguayo, G Lopez-Berestein, J-S Lee, A K Sood, M P Kim, G B Mills and 1 more

Abstract read
In one paragraph

Article in Oncogene, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
3.8field-weighted citation impact, top 6% 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

28 citing papers in PubMed, 41 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. The Role of miRNA in the Pathophysiology of Neuroendocrine Tumors.International journal of molecular sciences · 2021
    Review
  10. Article
  11. Article
  12. Tumor Suppressor Role of hsa-miR-193a-3p and -5p in Cutaneous Melanoma.International journal of molecular sciences · 2020
    Article
  13. Non-Coding RNAs in Lung Tumor Initiation and Progression.International journal of molecular sciences · 2020
    Review
  14. Inhibition ofAging · 2020
    Article
  15. Review
  16. Article
  17. The Roles of MicroRNA in Lung Cancer.International journal of molecular sciences · 2019
    Review
  18. Article
  19. Review
  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

11 authors at 3 institutions in 1 country.

E G SeviourDepartment of Systems Biology, UT MD Anderson Cancer Center, Houston, TX, USA.
V SehgalDepartment of Systems Biology, UT MD Anderson Cancer Center, Houston, TX, USA.
D MishraMethodist Hospital Research Institute, Houston, TX, USA.
R RupaimooleDepartment of Gynecologic Oncology, UTMDACC, Houston, TX, USA.
C Rodriguez-AguayoDepartment of Experimental Therapeutics, UTMDACC, Houston, TX, USA.ORCID 0000-0002-7880-7723
G Lopez-BeresteinDepartment of Experimental Therapeutics, UTMDACC, Houston, TX, USA.
J-S LeeDepartment of Systems Biology, UT MD Anderson Cancer Center, Houston, TX, USA.
A K SoodDepartment of Gynecologic Oncology, UTMDACC, Houston, TX, USA.
M P KimMethodist Hospital Research Institute, Houston, TX, USA.
G B MillsDepartment of Systems Biology, UT MD Anderson Cancer Center, Houston, TX, USA.
P T RamDepartment of Systems Biology, UT MD Anderson Cancer Center, Houston, TX, USA.
The University of Texas MD Anderson Cancer Center · USGynecologic Oncology Group · USHouston Methodist · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Fabien Delerue · 1985 to 2026
$290.8M
Systems-Based Predictions of Responses to Cancer TherapyU54CA112970 · NCI · UNIVERSITY OF CALIF-LAWRENC BERKELEY LAB · PI GRAY, JOE W. · 2004 to 2014
$27.1M
Novel extra cellular RNA-based combinatorial RNA inhibition therapyUH2TR000943 · NCATS · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI CALIN, GEORGE A., LOPEZ-BERESTEIN, GABRIEL · 2013 to 2014
$1.1M
NCATS NIH HHS UH2 TR000943NCI NIH HHS P30 CA016672NCI NIH HHS U54 CA112970
6 · The paper itself

Abstract

KRas is mutated in a significant number of human cancers and so there is an urgent therapeutic need to target KRas signalling. To target KRas in lung cancers we used a systems approach of integrating a genome-wide miRNA screen with patient-derived phospho-proteomic signatures of the KRas downstream pathway, and identified miR-193a-3p, which directly targets KRas. Unique aspects of miR-193a-3p biology include two functionally independent target sites in the KRas 3'UTR and clinically significant correlation between miR-193a-3p and KRas expression in patients. Rescue experiments with mutated KRas 3'UTR showed very significantly that the anti-tumour effect of miR-193a-3p is via specific direct targeting of KRas and not due to other targets. Ex vivo and in vivo studies utilizing nanoliposome packaged miR-193a-3p demonstrated significant inhibition of tumour growth, circulating tumour cell viability and decreased metastasis. These studies show the broader applicability of using miR-193a-3p as a therapeutic agent to target KRas-mutant cancer.

Indexed as

Gene Expression Regulation, NeoplasticRNA Interference3' Untranslated RegionsCell CycleCell Line, TumorDatabases, GeneticGenes, ReporterHumansMicroRNAsNeoplasm MetastasisNeoplasmsNeoplastic Cells, CirculatingProto-Oncogene Proteins p21(ras)RNA, Messenger3' Untranslated RegionsKRAS protein, humanMicroRNAsMIRN193 microRNA, humanProto-Oncogene Proteins p21(ras)RNA, Messenger

Identifiers

PMID27669434
PMCPMC5344721
OpenAlexW2524554744

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.