Evidence map›Paper›PMID 26103574›Full record

ArticleBritish journal of cancer2015

Dual inhibition of survivin and MAOA synergistically impairs growth of PTEN-negative prostate cancer.

S Xu, H Adisetiyo, S Tamura, F Grande, A Garofalo, P Roy-Burman, N Neamati

Open access · hybridAbstract read
In one paragraph

Article in British journal of cancer, 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
3.6field-weighted citation impact, top 7% 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, 34 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Review
  6. Article
  7. Inhibition of EZH2 and activation of ERRγ synergistically suppresses gastric cancer by inhibiting FOXM1 signaling pathway.Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association · 2021
    Article
  8. Article
  9. Article
  10. Dietary Protein Restriction Reprograms Tumor-Associated Macrophages and Enhances Immunotherapy.Clinical cancer research : an official journal of the American Association for Cancer Research · 2018
    Article
  11. Monoamine oxidase isoenzymes: genes, functions and targets for behavior and cancer therapy.Journal of neural transmission (Vienna, Austria : 1996) · 2018
    Review
  12. Article
  13. Hexokinase 2 is targetable for HK1 negative, HK2 positive tumors from a wide variety of tissues of origin.Journal of nuclear medicine : official publication, Society of Nuclear Medicine · 2018
    Article
  14. Evaluation of the Expression of Amine Oxidase Proteins in Breast Cancer.International journal of molecular sciences · 2017
    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 2 institutions in 2 countries.

S XuDepartment of Medicinal Chemistry, College of Pharmacy, Translational Oncology Program, University of Michigan, Ann Arbor, MI 48109, USA.
H AdisetiyoDepartment of Pathology, Keck School of Medicine, University of Southern California, Los Angeles, CA 90033, USA.
S TamuraDepartment of Medicinal Chemistry, College of Pharmacy, Translational Oncology Program, University of Michigan, Ann Arbor, MI 48109, USA.
F GrandeDipartimento di Farmacia e Scienze della Salute e della Nutrizione, Università della Calabria, Arcavacata di Rende, Italy.
A GarofaloDipartimento di Farmacia e Scienze della Salute e della Nutrizione, Università della Calabria, Arcavacata di Rende, Italy.
P Roy-BurmanDepartment of Pathology, Keck School of Medicine, University of Southern California, Los Angeles, CA 90033, USA.
N NeamatiDepartment of Medicinal Chemistry, College of Pharmacy, Translational Oncology Program, University of Michigan, Ann Arbor, MI 48109, USA.
University of Calabria · ITUniversity of Southern California · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSurvivin and monoamine oxidase A (MAOA) levels are elevated in prostate cancer (PCa) compared to normal prostate glands. However, the relationship between survivin and MAOA in PCa is unclear.

methodsWe examined MAOA expression in the prostate lobes of a conditional PTEN-deficient mouse model mirroring human PCa, with or without survivin knockout. We also silenced one gene at a time and examined the expression of the other. We further evaluated the combination of MAOA inhibitors and survivin suppressants on the growth, viability, migration and invasion of PCa cells.

resultsSurvivin and MAOA levels are both increased in clinical PCa tissues and significantly associated with patients' survival. Survivin depletion delayed MAOA increase during PCa progression, and silencing MAOA decreased survivin expression. The combination of MAOA inhibitors and the survivin suppressants (YM155 and SC144) showed significant synergy on the inhibition of PCa cell growth, migration and invasion with concomitant decrease in survivin and MMP-9 levels.

conclusionsThere is a positive feedback loop between survivin and MAOA expression in PCa. Considering that survivin suppressants and MAOA inhibitors are currently available in clinical trials and clinical use, their synergistic effects in PCa support a rapid translation of this combination to clinical practice.

Indexed as

AnimalsCell Line, TumorCell ProliferationDrug SynergismHumansHydrazinesInhibitor of Apoptosis ProteinsMaleMiceMonoamine OxidaseMonoamine Oxidase InhibitorsProstatic NeoplasmsPTEN PhosphohydrolaseQuinoxalinesSurvivinBIRC5 protein, humanHydrazinesInhibitor of Apoptosis ProteinsMonoamine OxidaseMonoamine Oxidase InhibitorsN'-(7-fluoroH-pyrrolo(1,2-a)quinoxalin-4-yl)pyrazine-2-carbohydrazidePTEN PhosphohydrolasePTEN protein, humanQuinoxalinesSurvivin

Identifiers

PMID26103574
PMCPMC4506394
OpenAlexW1534417549

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.