Evidence map›Paper›PMID 22213426›Full record

ArticleJournal of cellular physiology2012

Inactivation of Ink4a/Arf leads to deregulated expression of miRNAs in K-Ras transgenic mouse model of pancreatic cancer.

Shadan Ali, Sanjeev Banerjee, Farah Logna, Bin Bao, Philip A Philip, Murray Korc, Fazlul H Sarkar

RetractedAbstract readRetracted Publication
In one paragraph

Article in Journal of cellular physiology, 2012. 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 It has been retracted, and should not be counted.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 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing 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

30 citing papers in PubMed, 56 citations in OpenAlex.

  1. Pancreatic cancer stemness: dynamic status in malignant progression.Journal of experimental & clinical cancer research : CR · 2023
    Review
  2. Review
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  4. Article
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  7. Pancreatic Ductal Adenocarcinoma: Current and Evolving Therapies.International journal of molecular sciences · 2017
    Review
  8. Article
  9. Article
  10. Article
  11. Review
  12. MicroRNA Targeted Therapeutic Approach for Pancreatic Cancer.International journal of biological sciences · 2016
    Review
  13. Review
  14. Article
  15. Article
  16. Article
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  19. Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 3 institutions in 1 country.

Shadan AliDepartment of Oncology, Karmanos Cancer Institute, Wayne State University, Detroit, MI, USA.
Sanjeev Banerjee
Farah Logna
Bin Bao
Philip A Philip
Murray Korc
Fazlul H Sarkar
The Barbara Ann Karmanos Cancer Institute · USWayne State University · USIndiana University – Purdue University Indianapolis · US

Funding

Novel aspects of Epithelial-Mesenchymal Transition(EMT)in pancreatic cancerR01CA075059 · NCI · UNIVERSITY OF CALIFORNIA-IRVINE · PI KORC, MURRAY · 1997 to 2018
$4.3M
RO1: A novel and targeted approach to inhibit invasion and angiogenesisR01CA131151 · NCI · WAYNE STATE UNIVERSITY · PI SARKAR, FAZLUL H. · 2008 to 2012
$1.8M
Prevention of Tumor Progression by a Novel ApproachR01CA154321 · NCI · WAYNE STATE UNIVERSITY · PI SARKAR, FAZLUL H. · 2011 to 2015
$1.5M
FoxM1: A molecular target in pancreatic cancerR01CA132794 · NCI · WAYNE STATE UNIVERSITY · PI SARKAR, FAZLUL H. · 2009 to 2013
$1.5M
NCI NIH HHS 1R01CA132794NCI NIH HHS 3R01CA131151-02S109NCI NIH HHS 5R01CA131151NCI NIH HHS R01 CA075059NCI NIH HHS R01 CA131151NCI NIH HHS R01 CA132794NCI NIH HHS R01 CA154321
6 · The paper itself

Abstract

Human pancreatic cancer (PC) is an aggressive disease, which has been recapitulated in transgenic animal model that provides unique opportunity for mechanistic understanding of disease progression and also for testing the efficacy of novel therapeutics. Emerging evidence suggests deregulated expression of microRNAs (miRNAs) in human PC, and thus we investigated the expression of miRNAs in pancreas tissues obtained from transgenic mouse models of K-Ras (K), Pdx1-Cre (C), K-Ras;Pdx1-Cre (KC), and K-Ras;Pdx1-Cre;INK4a/Arf (KCI), initially from pooled RNA samples using miRNA profiling, and further confirmed in individual specimens by quantitative RT-PCR. We found over-expression of miR-21, miR-221, miR-27a, miR-27b, and miR-155, and down-regulation of miR-216a, miR-216b, miR-217, and miR-146a expression in tumors derived from KC and KCI mouse model, which was consistent with data from KCI-derived RInk-1 cells. Mechanistic investigations revealed a significant induction of EGFR, K-Ras, and MT1-MMP protein expression in tissues from both KC and KCI mouse compared to tissues from K or C, and these results were consistent with similar findings in RInk-1 cells compared to human MIAPaCa-2 cells. Furthermore, miR-155 knock-down in RInk-1 cells resulted in the inhibition of cell growth and colony formation consistent with down-regulation of EGFR, MT1-MMP, and K-Ras expression. In addition, miR-216b which target Ras, and forced re-expression of miR-216b in RInk-1 cells showed inhibition of cell proliferation and colony formation, which was correlated with reduced expression of Ras, EGFR, and MT1-MMP. These findings suggest that these models would be useful for preclinical evaluation of novel miRNA-targeted agents for designing personalized therapy for PC.

Indexed as

Genes, rasAnimalsCell LineCell ProliferationCyclin-Dependent Kinase Inhibitor p16Down-RegulationErbB ReceptorsGene Expression Regulation, NeoplasticHumansMatrix Metalloproteinase 14MiceMice, TransgenicMicroRNAsPancreasPancreatic NeoplasmsStem CellsCyclin-Dependent Kinase Inhibitor p16EGFR protein, mouseErbB ReceptorsMatrix Metalloproteinase 14MicroRNAsMmp14 protein, mouse

Identifiers

PMID22213426
PMCPMC3323695
OpenAlexW2013547705

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.