Evidence map›Paper›PMID 28496200›Full record

ArticleExperimental & molecular medicine2017

microRNA-200a-3p increases 5-fluorouracil resistance by regulating dual specificity phosphatase 6 expression.

Heejin Lee, Chongtae Kim, Hoin Kang, Hyosun Tak, Sojin Ahn, Sungjoo Kim Yoon, Hyo-Jeong Kuh, Wook Kim, Eun Kyung Lee

Open access · goldAbstract read
In one paragraph

Article in Experimental & molecular medicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.9field-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

23 citing papers in PubMed, 40 citations in OpenAlex.

  1. Article
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  5. MicroRNAs in T Cell-Immunotherapy.International journal of molecular sciences · 2022
    Review
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  8. Article
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  15. Exosomes Mediated Transfer of Circ_UBE2D2 Enhances the Resistance of Breast Cancer to Tamoxifen by Binding to MiR-200a-3p.Medical science monitor : international medical journal of experimental and clinical research · 2020
    Article
  16. Review
  17. Article
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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

9 authors at 2 institutions in 1 country.

Heejin LeeDepartment of Biochemistry, The Catholic University of Korea College of Medicine, Seoul, South Korea.
Chongtae KimDepartment of Biochemistry, The Catholic University of Korea College of Medicine, Seoul, South Korea.
Hoin KangDepartment of Biochemistry, The Catholic University of Korea College of Medicine, Seoul, South Korea.
Hyosun TakDepartment of Biochemistry, The Catholic University of Korea College of Medicine, Seoul, South Korea.
Sojin AhnDepartment of Biochemistry, The Catholic University of Korea College of Medicine, Seoul, South Korea.
Sungjoo Kim YoonDepartment of Medical Life Sciences, College of Medicine, The Catholic University of Korea, Seoul, South Korea.
Hyo-Jeong KuhDepartment of Medical Life Sciences, College of Medicine, The Catholic University of Korea, Seoul, South Korea.
Wook KimDepartment of Molecular Science and Technology, Ajou University, Suwon, South Korea.
Eun Kyung LeeDepartment of Biochemistry, The Catholic University of Korea College of Medicine, Seoul, South Korea.
Catholic University of Korea · KRAjou University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Acquisition of resistance to anti-cancer drugs is a significant obstacle to effective cancer treatment. Although several efforts have been made to overcome drug resistance in cancer cells, the detailed mechanisms have not been fully elucidated. Here, we investigated whether microRNAs (miRNAs) function as pivotal regulators in the acquisition of anti-cancer drug resistance to 5-fluorouracil (5-FU). A survey using a lentivirus library containing 572 precursor miRNAs revealed that five miRNAs promoted cell survival after 5-FU treatment in human hepatocellular carcinoma Hep3B cells. Among the five different clones, the clone expressing miR-200a-3p (Hep3B-miR-200a-3p) was further characterized as a 5-FU-resistant cell line. The cell viability and growth rate of Hep3B-miR-200a-3p cells were higher than those of control cells after 5-FU treatment. Ectopic expression of a miR-200a-3p mimic increased, while inhibition of miR-200a-3p downregulated, cell viability in response to 5-FU, doxorubicin, and CDDP (cisplatin). We also showed that dual-specificity phosphatase 6 (DUSP6) is a novel target of miR-200a-3p and regulates resistance to 5-FU. Ectopic expression of DUSP6 mitigated the pro-survival effects of miR-200a-3p. Taken together, these results lead us to propose that miR-200a-3p enhances anti-cancer drug resistance by decreasing DUSP6 expression.

Indexed as

Drug Resistance, NeoplasmAntineoplastic AgentsCell Line, TumorCisplatinDoxorubicinDual Specificity Phosphatase 6FluorouracilHumansMicroRNAsAntineoplastic AgentsCisplatinDoxorubicinDual Specificity Phosphatase 6DUSP6 protein, humanFluorouracilMicroRNAsMIRN200 microRNA, human

Identifiers

PMID28496200
PMCPMC5454440
OpenAlexW2612882398

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.