Evidence map›Paper›PMID 24865426›Full record

ArticleThe Journal of clinical investigation2014

Monoamine oxidase A mediates prostate tumorigenesis and cancer metastasis.

Jason Boyang Wu, Chen Shao, Xiangyan Li, Qinlong Li, Peizhen Hu, Changhong Shi, Yang Li, Yi-Ting Chen, Fei Yin, Chun-Peng Liao and 4 more

Open access · greenAbstract read
In one paragraph

Article in The Journal of clinical investigation, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 129 papers.

0numbers the graph read from it
0cells of the map it votes in
129citing papers in PubMed
5.0field-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

129 citing papers in PubMed, 228 citations in OpenAlex.

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  17. Synthesis of 1,2,4-Oxadiazin-5(6Molecules (Basel, Switzerland) · 2024
    Article
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69 more citing papers are in PubMed but not listed here.

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 2 institutions in 2 countries.

Jason Boyang Wu
Chen Shao
Xiangyan Li
Qinlong Li
Peizhen Hu
Changhong Shi
Yang Li
Yi-Ting Chen
Fei Yin
Chun-Peng Liao
Bangyan L Stiles
Haiyen E Zhau
Jean C Shih
Leland W K Chung
Cedars-Sinai Medical Center · USXijing Hospital · CN

Funding

Prostate Cancer Bone Metastasis: Biology and TargetingP01CA098912 · NCI · EMORY UNIVERSITY · PI ZAYZAFOON, MAJD · 2003 to 2019
$24.0M
The role of PTEN and AKT2 in the malignant transformation of liver progenitor celR01CA154986 · NCI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI STILES, BANGYAN · 2013 to 2017
$1.7M
Beta 2-Microglobulin signaling and targeting in bone metastasisR01CA122602 · NCI · CEDARS-SINAI MEDICAL CENTER · PI CHUNG, LELAND W.K. · 2009 to 2013
$1.5M
NCI NIH HHS 5P01CA098912NCI NIH HHS P01 CA098912NCI NIH HHS R01 CA122602NCI NIH HHS R01CA122602NCI NIH HHS R01 CA154986
6 · The paper itself

Abstract

Tumors from patients with high-grade aggressive prostate cancer (PCa) exhibit increased expression of monoamine oxidase A (MAOA), a mitochondrial enzyme that degrades monoamine neurotransmitters and dietary amines. Despite the association between MAOA and aggressive PCa, it is unclear how MAOA promotes PCa progression. Here, we found that MAOA functions to induce epithelial-to-mesenchymal transition (EMT) and stabilize the transcription factor HIF1α, which mediates hypoxia through an elevation of ROS, thus enhancing growth, invasiveness, and metastasis of PCa cells. Knockdown and overexpression of MAOA in human PCa cell lines indicated that MAOA induces EMT through activation of VEGF and its coreceptor neuropilin-1. MAOA-dependent activation of neuropilin-1 promoted AKT/FOXO1/TWIST1 signaling, allowing FOXO1 binding at the TWIST1 promoter. Importantly, the MAOA-dependent HIF1α/VEGF-A/FOXO1/TWIST1 pathway was activated in high-grade PCa specimens, and knockdown of MAOA reduced or even eliminated prostate tumor growth and metastasis in PCa xenograft mouse models. Pharmacological inhibition of MAOA activity also reduced PCa xenograft growth in mice. Moreover, high MAOA expression in PCa tissues correlated with worse clinical outcomes in PCa patients. These findings collectively characterize the contribution of MAOA in PCa pathogenesis and suggest that MAOA has potential as a therapeutic target in PCa.

Indexed as

AnimalsCarcinogenesisCell Line, TumorDisease ProgressionEpithelial-Mesenchymal TransitionForkhead Box Protein O1Forkhead Transcription FactorsGene Knockdown TechniquesHeterograftsHumansHypoxia-Inducible Factor 1, alpha SubunitMaleMiceMice, Inbred C57BLMice, NudeMice, SCIDForkhead Box Protein O1Forkhead Transcription FactorsFOXO1 protein, humanHIF1A protein, humanHypoxia-Inducible Factor 1, alpha SubunitMonoamine Oxidasemonoamine oxidase A, humanNuclear ProteinsTWIST1 protein, humanTwist-Related Protein 1Vascular Endothelial Growth Factor AVEGFA protein, human

Identifiers

PMID24865426
PMCPMC4071401
OpenAlexW2000158828

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.