Evidence map›Paper›PMID 28332309›Full record

ArticleCancer medicine2017

Effects of miR-145-5p through NRAS on the cell proliferation, apoptosis, migration, and invasion in melanoma by inhibiting MAPK and PI3K/AKT pathways.

Sha Liu, Guozhen Gao, Dexiong Yan, Xiangjun Chen, Xingwei Yao, Shuzhong Guo, Guirong Li, Yu Zhao

RetractedOpen access · goldAbstract readRetracted Publication
In one paragraph

Article in Cancer medicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It has been retracted, and should not be counted. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
5.1field-weighted citation impact, top 4% 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

44 citing papers in PubMed, 76 citations in OpenAlex.

  1. Review
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  4. Iranian journal of biotechnology · 2023
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4 · The record

Corrections and comments

  • Retraction · 2022-09-08Concerns/Issues about Results and/or Conclusions · Manipulation of Images · Objections by Third Party · Unreliable Results and/or Conclusions ·
  • Retracted
5 · Who and what money

Authors and funding

8 authors at 3 institutions in 1 country.

Sha LiuDepartment of Plastic and Reconstructive Surgery, Xijing Hospital, Fourth Military Medical University, Xi'an, 710032, China.
Guozhen GaoDepartment of Burn and Plastic Surgery, The 253rd Hospital of PLA, Hohhot, Inner Mongolia, 010051, China.
Dexiong YanDepartment of Burn and Plastic Surgery, The 253rd Hospital of PLA, Hohhot, Inner Mongolia, 010051, China.
Xiangjun ChenDepartment of Burn and Plastic Surgery, The 253rd Hospital of PLA, Hohhot, Inner Mongolia, 010051, China.
Xingwei YaoDepartment of Burn and Plastic Surgery, The 253rd Hospital of PLA, Hohhot, Inner Mongolia, 010051, China.
Shuzhong GuoDepartment of Plastic and Reconstructive Surgery, Xijing Hospital, Fourth Military Medical University, Xi'an, 710032, China.
Guirong LiDepartment of Otolaryngology-Head and Neck Surgery, The Fourth People's Hospital of Shaanxi Province, Xi'an, 710043, China.ORCID http://orcid.org/0000-0002-2052-3306
Yu ZhaoDepartment of Otolaryngology-Head and Neck Surgery, Xijing Hospital, Fourth Military Medical University, Xi'an, 710032, China.
Fourth Hospital of Inner Mongolia · CNXijing Hospital · CNThe Fourth People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We aimed to detect the effects of miR-145-5p on the cell proliferation, apoptosis, migration, and invasion in NRAS-mutant, BRAF-mutant, and wild-type melanoma cells, in order to figure out the potential mechanisms and provide a novel therapeutic target of melanoma. RT-qPCR and western blot were used to detect the expression of miR-145-5p and NRAS in melanoma tumor tissues and cells, respectively. Luciferase assay was performed to determine whether miR-145-5p directly targeted NRAS. After transfecting miR-145-5p mimics, miR-145-5p inhibitors, NRAS cDNA and NRAS siRNA into CHL-1, VMM917 and SK-mel-28 cells, functional assays were used to detect the proliferation, apoptosis, invasion and migration, including MTT, flow cytometry, Transwell and wound healing assays. In addition, xenograft models in nude mice were also conducted to verify the role of miR-145-5p in vivo. MiR-145-5p was able to suppress proliferation, invasion, and migration of VMM917 and CHL-1 cells and induce apoptosis by inhibiting MAPK and PI3K/AKT pathways. However, aberrant expression of miR-145-5p and NRAS has little impact on the viability and metastasis of BRAF-mutant melanoma. The higher expression of miR-145-5p in xenograft models repressed the VMM917-induced and CHL-1-induced tumor growth observably and has little effect on SK-mel-28-induced tumor growth which was consistent with the results in vitro. Through targeting NRAS, miR-145-5p could suppress cell proliferation, invasion, and migration and induce apoptosis of CHL-1 and VMM917 melanoma cells by inhibiting MAPK and PI3K/AKT pathways.

Indexed as

AdultAgedAnimalsApoptosisCell Line, TumorCell MovementCell ProliferationFemaleGTP PhosphohydrolasesHumansMaleMAP Kinase Signaling SystemMelanomaMembrane ProteinsMiceMicroRNAsGTP PhosphohydrolasesMembrane ProteinsMicroRNAsMIRN145 microRNA, humanNRAS protein, humanPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktMAPKmelanomamiR-145-5pNRAS

Identifiers

PMID28332309
PMCPMC5387172
OpenAlexW2600296286

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.