Evidence map›Paper›PMID 28411308›Full record

ArticlePathology oncology research : POR2018

The Effect of miR-200c Inhibition on Chemosensitivity (5- FluoroUracil) in Colorectal Cancer.

Korosh Heydari, Massoud Saidijam, Mohammad Reza Sharifi, Fatemeh Karimi Dermani, Sara Soleimani Asl, Nooshin Shabab, Rezvan Najafi

Abstract read
PubMed Publisher
In one paragraph

Article in Pathology oncology research : POR, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing 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

16 citing papers in PubMed, 38 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Review
  6. Review
  7. MicroRNA-Based Therapeutics for Drug-Resistant Colorectal Cancer.Pharmaceuticals (Basel, Switzerland) · 2021
    Review
  8. Review
  9. Review
  10. Article
  11. Article
  12. Expression of miRNA in 5-FU resistant esophageal cancer.Molecular and clinical oncology · 2020
    Article
  13. Review
  14. Review
  15. Article
  16. 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

7 authors at 2 institutions in 1 country.

Korosh HeydariResearch Center for Molecular Medicine, Hamadan University of Medical Sciences, Hamadan, Iran.
Massoud SaidijamResearch Center for Molecular Medicine, Hamadan University of Medical Sciences, Hamadan, Iran.
Mohammad Reza SharifiDepartment of Genetics and Molecular Biology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran.
Fatemeh Karimi DermaniResearch Center for Molecular Medicine, Hamadan University of Medical Sciences, Hamadan, Iran.
Sara Soleimani AslDepartment of Anatomy, Faculty of Medicine, Hamadan University of Medical Sciences, Hamadan, Iran.
Nooshin ShababResearch Center for Molecular Medicine, Hamadan University of Medical Sciences, Hamadan, Iran.
Rezvan NajafiResearch Center for Molecular Medicine, Hamadan University of Medical Sciences, Hamadan, Iran. re.najafi@umsha.ac.ir.
Hamedan University of Medical Sciences · IRIsfahan University of Medical Sciences · IR

Funding

Hamadan University of Medical Sciences 9407073722
6 · The paper itself

Abstract

5-Fluorouracil (5-FU) as a chemotherapeutic drug is used to treat colorectal cancer (CRC). However, 5-FU is associated with acquired CRC resistance, which decreases the therapeutic potential of 5-FU. Several studies indicated that miR-200c is also involved in chemotherapeutic drug resistance, but the exact mechanism of miR-200c mediated chemoresistance has not yet been fully understood. In this study, we examined the effect of inhibition of miR-200c on the sensitivity of HCT-116 cells to 5-FU. HCT-116 cells were transfected with LNA-anti- miR-200c for 48 h. mRNA expression of miR-200c was investigated by qRT-PCR. The protein expression of phosphatase and tensin homolog (PTEN) and E-cadherin were evaluated by western blotting. Annexin V/ PI staining and caspase 3 activity were used to detect apoptosis. LNA-anti-miR-200c inhibited the miR-200c expression in the transfected cells compared with that in the control group. LNA-anti-miR-200c suppressed the expression of PTEN and E-cadherin independent of the presence of the chemotherapeutic drug 5-FU. LNA-anti-miR-200c reduced the 5-FU-induced apoptosis and caspase 3 activity. miR-200c, as a novel prognostic marker in CRC, can be a potential therapeutic approach to overcome chemoresistance during 5-FU chemotherapy.

Indexed as

Antigens, CDAntimetabolites, AntineoplasticApoptosisCadherinsCell ProliferationColorectal NeoplasmsDrug Resistance, NeoplasmFluorouracilGene Expression Regulation, NeoplasticHumansMicroRNAsPTEN PhosphohydrolaseTumor Cells, CulturedAntigens, CDAntimetabolites, AntineoplasticCadherinsCDH1 protein, humanFluorouracilMicroRNAsMIRN200 microRNA, humanPTEN PhosphohydrolasePTEN protein, human5-FU resistanceColorectal cancerE-cadherinmiR-200cPTEN

Identifiers

PMID28411308
OpenAlexW2606652278

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.