Evidence map›Paper›PMID 26261515›Full record

ArticleInternational journal of clinical and experimental pathology2015

MiR-218 inhibits multidrug resistance (MDR) of gastric cancer cells by targeting Hedgehog/smoothened.

Xiang-Liang Zhang, Hui-Juan Shi, Ji-Ping Wang, Hong-Sheng Tang, Shu-Zhong Cui

Open access · greenAbstract read
In one paragraph

Article in International journal of clinical and experimental pathology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

14 citing papers in PubMed, 36 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Non-coding RNAs underlying chemoresistance in gastric cancer.Cellular oncology (Dordrecht, Netherlands) · 2020
    Review
  5. Observational
  6. Review
  7. Article
  8. Non-coding RNA in drug resistance of gastric cancer.World journal of gastrointestinal oncology · 2019
    Review
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Emerging Role of miRNAs in the Drug Resistance of Gastric Cancer.International journal of molecular sciences · 2016
    Review
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 3 institutions in 2 countries.

Xiang-Liang ZhangDepartment of Abdominal Surgery (Section 2), Affiliated Cancer Hospital of Guangzhou Medical University 78 Hengzhigang Road, Guangzhou, Guangdong 510095, China.
Hui-Juan ShiDepartment of Pathology, The First Affiliated Hospital of Sun Yat-Sen University 58 Zhongshan Er Rd, Guangzhou, Guangdong 510080, China.
Ji-Ping WangDepartment of Surgery, Brigham and Women's Hospital and Harvard Medical School and Departments of Surgery and Pathology, Massachusetts General Hospital and Harvard Medical School Boston, MA, USA.
Hong-Sheng TangDepartment of Abdominal Surgery (Section 2), Affiliated Cancer Hospital of Guangzhou Medical University 78 Hengzhigang Road, Guangzhou, Guangdong 510095, China.
Shu-Zhong CuiDepartment of Abdominal Surgery (Section 2), Affiliated Cancer Hospital of Guangzhou Medical University 78 Hengzhigang Road, Guangzhou, Guangdong 510095, China.
Guangzhou Medical University Cancer Hospital · CNBrigham and Women's Hospital · USSun Yat-sen University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Multidrug resistance (MDR) is the main obstacle to successful chemotherapy for patients with gastric cancer. The microRNA miR-218 influences various pathobiological processes in gastric cancer, and its down-regulation in this disease raises the question of whether it normally inhibits MDR. In this study we observed that two MDR gastric cancer cell lines showed lower expression of miR-218 compared with their chemosensitive parental cell line. Overexpressing miR-218 chemosensitizes gastric cancer cells, slowed efflux of adriamycin, and accelerated drug-induced apoptosis. We identified the smoothened (SMO) gene as a functional target of miR-218, and found that SMO overexpression counteracts the chemosensitizing effects of miR-218. These findings suggest that miR-218 inhibits MDR of gastric cancer cells by down-regulating SMO expression.

Indexed as

Blotting, WesternCell Line, TumorDrug Resistance, MultipleDrug Resistance, NeoplasmFlow CytometryGene Expression Regulation, NeoplasticHedgehog ProteinsHumansMicroRNAsReal-Time Polymerase Chain ReactionReceptors, G-Protein-CoupledSmoothened ReceptorStomach NeoplasmsTransfectionHedgehog ProteinsMicroRNAsMIRN218 microRNA, humanReceptors, G-Protein-CoupledSmoothened ReceptorSMO protein, humanGastric cancerhedgehoghsa-miR-218multi-drug resistanceSMO

Identifiers

PMID26261515
PMCPMC4525849
OpenAlexW2410111424

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.