Evidence map›Paper›PMID 25991669›Full record

ArticleOncotarget2015

The miR-193a-3p-regulated ING5 gene activates the DNA damage response pathway and inhibits multi-chemoresistance in bladder cancer.

Yang Li, Hui Deng, Lei Lv, Cheng Zhang, Liting Qian, Jun Xiao, Weidong Zhao, Qi Liu, Daming Zhang, Yingwei Wang and 4 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
5.3field-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

38 citing papers in PubMed, 64 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Review
  6. The roles of ING5 in cancer: A tumor suppressor.Frontiers in cell and developmental biology · 2022
    Review
  7. Article
  8. Article
  9. Article
  10. The mStem cells international · 2020
    Article
  11. Article
  12. The mOncogene · 2019
    Article
  13. MiR-34b-3p Represses the Multidrug-Chemoresistance of Bladder Cancer Cells by Regulating the CCND2 and P2RY1 Genes.Medical science monitor : international medical journal of experimental and clinical research · 2019
    Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  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

14 authors at 5 institutions in 1 country.

Yang LiDepartment of Biology, School of Life Science, Anhui Medical University, Hefei, Anhui, China.
Hui DengCancer Epigenetics Program, Anhui Cancer Hospital, Hefei, Anhui, China.
Lei LvCancer Epigenetics Program, Anhui Cancer Hospital, Hefei, Anhui, China.
Cheng ZhangDepartment of Urology, The First Affiliated Hospital of Harbin Medical University, Harbin, Heilongjiang Province, China.
Liting QianDepartment of Radiotherapy, Anhui Cancer Hospital, Hefei, Anhui, China.
Jun XiaoDepartment of Urology, Anhui Provincial Hospital, Hefei, Anhui, China.
Weidong ZhaoDepartment of Gynecologic Cancer, Anhui Cancer Hospital, Hefei, Anhui, China.
Qi LiuSchool of Life Science and Technology, State Key Laboratory of Urban Water Resource and Environment, Harbin Institute of Technology, Harbin, Heilongjiang, China.
Daming ZhangDepartment of Neurosurgery, The First Affiliated Hospital of Harbin Medical University, Harbin, Heilongjiang Province, China.
Yingwei WangDepartment of Pathology, The First Affiliated Hospital of Harbin Medical University, Harbin, Heilongjiang Province, China.
Jun YanDepartment of Urology, The First Affiliated Hospital of Harbin Medical University, Harbin, Heilongjiang Province, China.
Hongyu ZhangCancer Epigenetics Program, Shanghai Cancer Institute, Renji Hospital, Shanghai Jiaotong University, Shanghai, China.
Yinghua HeCancer Epigenetics Program, Shanghai Cancer Institute, Renji Hospital, Shanghai Jiaotong University, Shanghai, China.
Jingde ZhuCancer Epigenetics Program, Anhui Cancer Hospital, Hefei, Anhui, China.
Anhui Provincial Hospital · CNHarbin Medical University · CNShanghai Cancer Institute · CNAnhui Medical University · CNHarbin Institute of Technology · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

As the major barrier to curative cancer chemotherapy, chemoresistance presents a formidable challenge to both cancer researchers and clinicians. We have previously shown that the bladder cancer (BCa) cell line 5637 is significantly more sensitive to the cytoxicity of five chemotherapeutic agents than H-bc cells. Using an RNA-seq-based omic analysis and validation at both the mRNA and protein levels, we found that the inhibitor of growth 5 (ING5) gene was upregulated in 5637 cells compared with H-bc cells, indicating that it has an inhibitory role in BCa chemoresistance. siRNA-mediated inhibition of ING5 increased the chemoresistance and inhibited the DNA damage response pathway in 5637 cells. Conversely, forced expression of EGFP-ING5 decreased the chemoresistance of and activated the DNA damage response pathway in H-bc cells. We also showed that ING5 gene expression is inhibited by miR-193a-3p and is instrumental in miR-193a-3p's role in activating BCa chemoresistance. Our results demonstrate both the role and mechanism of inhibition of BCa chemoresistance by ING5.

Indexed as

DNA DamageAcetylationAnimalsAntineoplastic AgentsCell Line, TumorDrug Resistance, NeoplasmGene Expression Regulation, NeoplasticHumansMiceMice, NudeMicroRNAsSignal TransductionTranscription FactorsTransfectionTumor Suppressor ProteinsUrinary Bladder NeoplasmsAntineoplastic AgentsING5 protein, humanMicroRNAsMIRN193 microRNA, humanTranscription FactorsTumor Suppressor Proteinsbladder cancerchemoresistanceING5miR-193a-3pprotein acetylation

Identifiers

PMID25991669
PMCPMC4496349
OpenAlexW2163192311

What OpenQuestion holds

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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.