Evidence map›Paper›PMID 25833695›Full record

ArticleTumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine2015

MiR-197 induces Taxol resistance in human ovarian cancer cells by regulating NLK.

Dongling Zou, Dong Wang, Rong Li, Ying Tang, Li Yuan, Xingtao Long, Qi Zhou

Abstract read
PubMed Publisher
In one paragraph

Article in Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
2.6field-weighted citation impact, top 11% 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

26 citing papers in PubMed, 45 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Review
  6. Review
  7. Article
  8. Review
  9. Article
  10. Review
  11. Article
  12. Review
  13. Progress in research on paclitaxel and tumor immunotherapy.Cellular & molecular biology letters · 2019
    Review
  14. Article
  15. MiR-101: a potential therapeutic target of cancers.American journal of translational research · 2018
    Review
  16. Review
  17. Article
  18. miR-134: A Human Cancer Suppressor?Molecular therapy. Nucleic acids · 2017
    Review
  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

7 authors at 1 institution in 1 country.

Dongling ZouDepartment of Gynecologic Oncology, Chongqing Cancer Institute, Chongqing, 400030, China.
Dong WangDepartment of Gynecologic Oncology, Chongqing Cancer Institute, Chongqing, 400030, China.
Rong LiDepartment of Gynecologic Oncology, Chongqing Cancer Institute, Chongqing, 400030, China.
Ying TangDepartment of Gynecologic Oncology, Chongqing Cancer Institute, Chongqing, 400030, China.
Li YuanDepartment of Gynecologic Oncology, Chongqing Cancer Institute, Chongqing, 400030, China.
Xingtao LongDepartment of Gynecologic Oncology, Chongqing Cancer Institute, Chongqing, 400030, China.
Qi ZhouDepartment of Gynecologic Oncology, Chongqing Cancer Institute, Chongqing, 400030, China. qizhou9128@163.com.
Chongqing Cancer Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chemotherapy is the preferred therapeutic approach for the therapy of advanced ovarian cancer, but 5-year survival rate remains low due to the development of drug resistance. Increasing evidence has documented that microRNAs (miRNAs) act important roles in drug resistance in a variety types of cancer. However, the roles of miRNA in regulating Taxol resistance in ovarian cancer and the detailed mechanism are less reported. We used Taqman probe stem loop real-time PCR to accurately measure the levels of miR-197 in normal ovarian cells, ovarian cancer cells, and Taxol-resistant ovarian cancer cells and found that miR-197 was significantly increased in Taxol-resistant ovarian cancer cells. Enforced expression of miR-197 can promote Taxol resistance, cell proliferation, and invasion of ovarian cancer cells. Meanwhile, repression of miR-197 in ovarian cancer cells can sensitize its response to Taxol and also induced attenuated cell proliferation and invasion ability. Furthermore, investigation of the detailed mechanism showed that the promotion of miR-197 on drug resistance in ovarian cancer cells was partially mediated by downregulating NLK, a negative regulator of WNT signaling pathway. Taken together, our work first demonstrated that miR-197 can confer drug resistance to Taxol, by regulating tumor suppressor, NLK expression in ovarian cancer cells.

Indexed as

Cell Line, TumorCell ProliferationDrug Resistance, NeoplasmFemaleGene Expression Regulation, NeoplasticHumansIntracellular Signaling Peptides and ProteinsMicroRNAsOvarian NeoplasmsPaclitaxelProtein Serine-Threonine KinasesIntracellular Signaling Peptides and ProteinsMicroRNAsMIRN197 microRNA, humanNLK protein, humanPaclitaxelProtein Serine-Threonine KinasesDrug resistancemiR-197NLKOvarian cancerTaxol

Identifiers

PMID25833695
OpenAlexW2087464591

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.