Evidence map›Paper›PMID 26878873›Full record

ArticleBMC cancer2016

MiR-193b promotes autophagy and non-apoptotic cell death in oesophageal cancer cells.

Michelle J Nyhan, Tracey R O'Donovan, Antonius W M Boersma, Erik A C Wiemer, Sharon L McKenna

Open access · goldAbstract read
In one paragraph

Article in BMC cancer, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
3.3field-weighted citation impact, top 8% 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

33 citing papers in PubMed, 61 citations in OpenAlex.

  1. Article
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  8. Autophagy in gastrointestinal cancers.Frontiers in oncology · 2022
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  9. Article
  10. Virus, Exosome, and MicroRNA: New Insights into Autophagy.Advances in experimental medicine and biology · 2022
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  11. Review
  12. The Emerging Roles of Autophagy-Related MicroRNAs in Cancer.International journal of biological sciences · 2021
    Review
  13. Review
  14. Review
  15. Autophagy in cancers including brain tumors: role of MicroRNAs.Cell communication and signaling : CCS · 2020
    Review
  16. Article
  17. Article
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  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

5 authors at 2 institutions in 2 countries.

Michelle J NyhanCork Cancer Research Centre, 4th Floor Western Gateway Building, University College Cork, Cork, Ireland. michellenyhan@yahoo.co.uk.
Tracey R O'DonovanCork Cancer Research Centre, 4th Floor Western Gateway Building, University College Cork, Cork, Ireland. tracey.odonovan@ucc.ie.
Antonius W M BoersmaDepartment of Medical Oncology, Erasmus MC Cancer Institute, Erasmus University Medical Center, Rotterdam, The Netherlands. a.boersma@erasmusmc.nl.
Erik A C WiemerDepartment of Medical Oncology, Erasmus MC Cancer Institute, Erasmus University Medical Center, Rotterdam, The Netherlands. e.wiemer@erasmusmc.nl.
Sharon L McKennaCork Cancer Research Centre, 4th Floor Western Gateway Building, University College Cork, Cork, Ireland. s.mckenna@ucc.ie.
University College Cork · IEErasmus MC · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSuccessful treatment of oesophageal cancer is hampered by recurrent drug resistant disease. We have previously demonstrated the importance of apoptosis and autophagy for the recovery of oesophageal cancer cells following drug treatment. When apoptosis (with autophagy) is induced, these cells are chemosensitive and will not recover following chemotherapy treatment. In contrast, when cancer cells exhibit only autophagy and limited Type II cell death, they are chemoresistant and recover following drug withdrawal.

methodsMicroRNA (miRNA) expression profiling of an oesophageal cancer cell line panel was used to identify miRNAs that were important in the regulation of apoptosis and autophagy. The effects of miRNA overexpression on cell death mechanisms and recovery were assessed in the chemoresistant (autophagy inducing) KYSE450 oesophageal cancer cells.

resultsMiR-193b was the most differentially expressed miRNA between the chemosensitive and chemoresistant cell lines with higher expression in chemosensitive apoptosis inducing cell lines. Colony formation assays showed that overexpression of miR-193b significantly impedes the ability of KYSE450 cells to recover following 5-fluorouracil (5-FU) treatment. The critical mRNA targets of miR-193b are unknown but target prediction and siRNA data analysis suggest that it may mediate some of its effects through stathmin 1 regulation. Apoptosis was not involved in the enhanced cytotoxicity. Overexpression of miR-193b in these cells induced autophagic flux and non-apoptotic cell death.

conclusionThese results highlight the importance of miR-193b in determining oesophageal cancer cell viability and demonstrate an enhancement of chemotoxicity that is independent of apoptosis induction.

Indexed as

Antineoplastic AgentsApoptosisAutophagyCell Line, TumorCell SurvivalDrug Resistance, NeoplasmEsophageal NeoplasmsFluorouracilHumansMicroRNAsAntineoplastic AgentsFluorouracilMicroRNAsMIRN193 microRNA, human

Identifiers

PMID26878873
PMCPMC4754993
OpenAlexW2284017961

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.