Evidence map›Paper›PMID 26261493›Full record

ArticleInternational journal of clinical and experimental pathology2015

Synergistic effects of snail and quercetin on renal cell carcinoma Caki-2 by altering AKT/mTOR/ERK1/2 signaling pathways.

Fan-Dong Meng, Yan Li, Xin Tian, Ping Ma, Cheng-Guang Sui, Li-Ye Fu, You-Hong Jiang

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 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.7field-weighted citation impact, top 17% 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

17 citing papers in PubMed, 32 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Review
  6. Review
  7. Article
  8. Review
  9. Quercetin Inhibits the Migration and Invasion of HCCLM3 Cells by Suppressing the Expression of p-Akt1, Matrix Metalloproteinase (MMP) MMP-2, and MMP-9.Medical science monitor : international medical journal of experimental and clinical research · 2018
    Article
  10. Article
  11. Flavonoids in Kidney Health and Disease.Frontiers in physiology · 2018
    Review
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. 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.

Fan-Dong MengDepartment of Molecular Oncology, Cancer Research Institution, The First Affiliated Hospital of China Medical University Shenyang 110001, Liaoning Province, China.
Yan LiDepartment of Molecular Oncology, Cancer Research Institution, The First Affiliated Hospital of China Medical University Shenyang 110001, Liaoning Province, China.
Xin TianDepartment of Molecular Oncology, Cancer Research Institution, The First Affiliated Hospital of China Medical University Shenyang 110001, Liaoning Province, China.
Ping MaDepartment of Molecular Oncology, Cancer Research Institution, The First Affiliated Hospital of China Medical University Shenyang 110001, Liaoning Province, China.
Cheng-Guang SuiDepartment of Molecular Oncology, Cancer Research Institution, The First Affiliated Hospital of China Medical University Shenyang 110001, Liaoning Province, China.
Li-Ye FuDepartment of Molecular Oncology, Cancer Research Institution, The First Affiliated Hospital of China Medical University Shenyang 110001, Liaoning Province, China.
You-Hong JiangDepartment of Molecular Oncology, Cancer Research Institution, The First Affiliated Hospital of China Medical University Shenyang 110001, Liaoning Province, China.
First Hospital of China Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Renal cell carcinoma has become the most common subtype of kidney cancer, and has the highest propensity to manifest as metastatic disease. Because of lack of knowledge in events that correlated with tumor cell migration and invasion, few therapeutic options are available. Therefore, in current study, we explore the anti-tumoral effect of a potential chemopreventive natural product, quercetin, combined with anti-sense oligo gene therapy (inhibiting Snail gene). We found that either one of them had the remarkable effects in suppressing cell proliferation and migration, inducing cell cycle arrest and apoptosis in a ccRCC cell line, Caki-2 cells. The combination of both means provides even strong suppressive effects toward these ccRCC cells. Our study, for the first time, provides the possibility of using a novel treatment for renal cancer, by combining natural product and gene therapy.

Indexed as

RNAi TherapeuticsAntineoplastic AgentsApoptosisCarcinoma, Renal CellCell Line, TumorCell MovementCell ProliferationEnzyme ActivationGene Expression Regulation, NeoplasticHumansKidney NeoplasmsMitogen-Activated Protein Kinase 1Mitogen-Activated Protein Kinase 3Neoplasm InvasivenessPhosphorylationProto-Oncogene Proteins c-aktAntineoplastic AgentsMAPK1 protein, humanMitogen-Activated Protein Kinase 1Mitogen-Activated Protein Kinase 3MTOR protein, humanProto-Oncogene Proteins c-aktQuercetinRNA, Small InterferingSnail Family Transcription FactorsTOR Serine-Threonine KinasesTranscription FactorsAKT/mTOR/ERK1/2quercetinrenal cell carcinomaSnail

Identifiers

PMID26261493
PMCPMC4525827
OpenAlexW1192308178

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.