Evidence map›Paper›PMID 25611699›Full record

ArticleCancer biology & therapy2015

Down regulation of miR-202 modulates Mxd1 and Sin3A repressor complexes to induce apoptosis of pancreatic cancer cells.

Lulu Farhana, Marcia I Dawson, Joseph A Fontana

Open access · bronzeAbstract read
In one paragraph

Article in Cancer biology & therapy, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 1 pooled it
2.0field-weighted citation impact, top 15% 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

25 citing papers in PubMed, 1 synthesis or guideline pooled it, 39 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Myc beyond Cancer: Regulation of Mammalian Tissue Regeneration.Pathophysiology : the official journal of the International Society for Pathophysiology · 2023
    Review
  4. Review
  5. Review
  6. The microRNA-202 as a Diagnostic Biomarker and a Potential Tumor Suppressor.International journal of molecular sciences · 2022
    Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Diverse regulatory manners of human telomerase reverse transcriptase.Cell communication and signaling : CCS · 2019
    Review
  13. Article
  14. Article
  15. Overexpression ofBioscience reports · 2018
    Article
  16. Review
  17. Oncomirs Expression Profiling in Uterine Leiomyosarcoma Cells.International journal of molecular sciences · 2017
    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

3 authors at 2 institutions in 1 country.

Lulu Farhanaa John D Dingell VA Medical Center; Department of Oncology ; Detroit , MI USA.
Marcia I Dawson
Joseph A Fontana
Wayne State University · USLa Jolla Alcohol Research · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Aberrant regulation of microRNA expression in pancreatic cancers has been shown to play an important role in its inherent poor prognosis and malignant potential. MicroRNAs have also been shown to inhibit translation of genes by targeting the 3'-untranslated region (3-UTR) of mRNAs resulting in the inhibition of translation and often destruction of the mRNA. In the present study we investigated the role of the microRNA miR-202 in the apoptotic pathways of pancreatic cancer cells. The adamantyl-related molecule, 3-Cl-AHPC down-regulated expression of miR-202 and miR-578 resulting in the increased expression of mRNA and protein expression of their target genes, Max dimerization protein 1 (Mxd1/Mad1) and the Sin3A associated protein 18 (SAP18). Overexpression of pre-miR-202 led to diminished levels of Mxd1 and blocked the 3-Cl-AHPC-mediated increase in Mxd1 mRNA expression. The addition of the microRNA inhibitor 2'-O-methylated miR-202 enhanced the 3-Cl-AHPC-mediated increase of Mxd1 mRNA levels as well as 3-CI-AHPC-mediated apoptosis. We found increased Mxd1 bound to the Sin3A repressor protein complex through its increased binding with HDAC-2 and subsequently enhanced transcriptional repression in cells as evidenced by increased HDAC activity. Mxd1 also repressed human telomerase reverse transcriptase (hTERT) mRNA expression through its increased binding to the hTERT promoter site and resulted in decreased telomerase activity in cells. Our results demonstrate that down regulation of miR-202 increased the expression of its target Mxd1, followed by Mxd1 recruitment to the Sin3A repressor complex and through its dimerization with Max, and increased repression of Myc-Max target proteins.

Indexed as

Gene Expression Regulation, Neoplastic3' Untranslated RegionsAdamantaneApoptosisBasic Helix-Loop-Helix Leucine Zipper Transcription FactorsCell Line, TumorCinnamatesHumansMicroRNAsPancreatic NeoplasmsProtein BindingRepressor ProteinsRNA InterferenceSin3 Histone Deacetylase and Corepressor ComplexTelomerase3' Untranslated Regions4-(3-(1-adamantyl)-4-hydroxyphenyl)-3-chlorocinnamic acidAdamantaneBasic Helix-Loop-Helix Leucine Zipper Transcription FactorsCinnamatesMicroRNAsMIRN202 microRNA, humanMXD1 protein, humanRepressor ProteinsSIN3A transcription factorSin3 Histone Deacetylase and Corepressor ComplexTelomeraseTERT protein, human3-Cl-AHPC, (E)-4-[3-(1-adamantyl)-4-hydroxyphenyl]-3-chlorocinnamic acidARR, Adamantly-substituted retinoid relatedc-MycHDCA2, histone deacetylase 2hTERThTERT, human telomerase reverse transcriptasemiR-202miR-578Mxd1/Mad1Mxd1, Max dimerization protein 1pancreatic cancerSAP18SAP18, Sin3A associated protein 18Sin3A

Identifiers

PMID25611699
PMCPMC4623045
OpenAlexW2087801876

What OpenQuestion holds

Textmetadata
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.