Evidence map›Paper›PMID 32066880›Full record

ArticleOncogene2020

MAOA-mediated reprogramming of stromal fibroblasts promotes prostate tumorigenesis and cancer stemness.

Jingjing Li, Tianjie Pu, Lijuan Yin, Qinlong Li, Chun-Peng Liao, Boyang Jason Wu

Abstract read
PubMed Publisher
In one paragraph

Article in Oncogene, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
3.6field-weighted citation impact, top 6% 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

32 citing papers in PubMed, 48 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Review
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Review
  16. Review
  17. Article
  18. Telomere dysfunction in Tert knockout mice delays BrafInternational journal of cancer · 2024
    Article
  19. Review
  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

6 authors at 6 institutions in 2 countries.

Jingjing Li *Department of Pharmaceutical Sciences, College of Pharmacy and Pharmaceutical Sciences, Washington State University, 205 E Spokane Falls Blvd, PBS 421, Spokane, WA, 99202, USA.
Tianjie Pu *Department of Pharmaceutical Sciences, College of Pharmacy and Pharmaceutical Sciences, Washington State University, 205 E Spokane Falls Blvd, PBS 421, Spokane, WA, 99202, USA.
Lijuan YinDepartment of Pathology, West China Hospital, Sichuan University, Chengdu, Sichuan, 610041, China.
Qinlong LiDepartment of Pathology, Xijing Hospital, Medical University of the Air Force, Xi'an, Shaanxi, 710032, China.
Chun-Peng LiaoLawrence J. Ellison Institute for Transformative Medicine, Keck School of Medicine, University of Southern California, Los Angeles, CA, 90089, USA.
Boyang Jason WuDepartment of Pharmaceutical Sciences, College of Pharmacy and Pharmaceutical Sciences, Washington State University, 205 E Spokane Falls Blvd, PBS 421, Spokane, WA, 99202, USA. boyang.wu@wsu.edu.
Cedars-Sinai Medical Center · USShanghai Jiao Tong University · CNSichuan University · CNUniversity of Southern California · USWashington State University Spokane · USXijing Hospital · CN

Funding

MAOA and AR Reciprocal Crosstalk in Prostate CancerR37CA233658 · NCI · WASHINGTON STATE UNIVERSITY · PI WU, BOYANG · 2019 to 2025
$2.4M
U.S. Department of Health & Human Services | National Institutes of Health (NIH) R37CA233658
6 · The paper itself

Abstract

The tumor microenvironment plays a critical role in prostate cancer (PC) development and progression. Inappropriate activation of the stroma potentiates the growth and transformation of epithelial tumor cells. Here, we show that upregulation of monoamine oxidase A (MAOA), a mitochondrial enzyme that degrades monoamine neurotransmitters and dietary amines, in stromal cells elevates production of reactive oxygen species, triggers an inflammatory response including activation of IL-6, and promotes tumorigenesis in vitro and in vivo. Mechanistically, MAOA enhances IL-6 transcription through direct Twist1 binding to a conserved E-box element at the IL-6 promoter. MAOA in stromal fibroblasts provides tumor cell growth advantages through paracrine IL-6/STAT3 signaling. Tissue microarray analysis revealed co-expression correlations between individual pairs of proteins of the stromal MAOA-induced Twist1/IL-6/STAT3 pathway in clinical specimens. Downstream of stromal MAOA, STAT3 also promotes cell stemness and transcriptionally activates expression of cancer stem cell marker CD44 in PC cells. MAOA inhibitor treatment effectively suppressed prostate tumor growth in mice in a stroma-specific targeted manner. Collectively, these findings characterize the contribution of MAOA to stromal activation in PC pathogenesis and provide a rationale for targeting MAOA in stromal cells to treat PC.

Indexed as

AnimalsCarcinogenesisCell ProliferationCellular ReprogrammingFibroblastsHeterograftsHumansInterleukin-6MaleMiceMonoamine OxidaseMonoamine Oxidase InhibitorsNuclear ProteinsProstatic NeoplasmsSTAT3 Transcription FactorTumor MicroenvironmentInterleukin-6Monoamine Oxidasemonoamine oxidase A, humanMonoamine Oxidase InhibitorsNuclear ProteinsSTAT3 Transcription FactorTWIST1 protein, humanTwist-Related Protein 1

Identifiers

PMID32066880
OpenAlexW3006273062

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.