Evidence map›Paper›PMID 32681068›Full record

ArticleOncogene2020

MEIS1 down-regulation by MYC mediates prostate cancer development through elevated HOXB13 expression and AR activity.

Nichelle C Whitlock, Shana Y Trostel, Scott Wilkinson, Nicholas T Terrigino, S Thomas Hennigan, Ross Lake, Nicole V Carrabba, Rayann Atway, Elizabeth D Walton, Berkley E Gryder and 3 more

Open access · hybridAbstract read
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 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.4field-weighted citation impact, top 9% 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. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Streamlined identification of clinically and functionally relevant genetic regulators of lower-tract urogenital development.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  7. Review
  8. The impact ofAnimal cells and systems · 2024
    Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. [miR-20a-5p inhibits proliferation of lung cancer A549 cells by down-regulating HOXB13].Nan fang yi ke da xue xue bao = Journal of Southern Medical University · 2022
    Article
  14. Article
  15. Review
  16. MEIS1 and its potential as a cancer therapeutic target (Review).International journal of molecular medicine · 2021
    Review
  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

13 authors at 2 institutions in 1 country.

Nichelle C WhitlockLaboratory of Genitourinary Cancer Pathogenesis, National Cancer Institute, NIH, Bethesda, MD, 20892, USA.
Shana Y TrostelLaboratory of Genitourinary Cancer Pathogenesis, National Cancer Institute, NIH, Bethesda, MD, 20892, USA.
Scott WilkinsonLaboratory of Genitourinary Cancer Pathogenesis, National Cancer Institute, NIH, Bethesda, MD, 20892, USA.ORCID http://orcid.org/0000-0002-2613-8425
Nicholas T TerriginoLaboratory of Genitourinary Cancer Pathogenesis, National Cancer Institute, NIH, Bethesda, MD, 20892, USA.ORCID http://orcid.org/0000-0002-0829-8433
S Thomas HenniganLaboratory of Genitourinary Cancer Pathogenesis, National Cancer Institute, NIH, Bethesda, MD, 20892, USA.
Ross LakeLaboratory of Genitourinary Cancer Pathogenesis, National Cancer Institute, NIH, Bethesda, MD, 20892, USA.
Nicole V CarrabbaLaboratory of Genitourinary Cancer Pathogenesis, National Cancer Institute, NIH, Bethesda, MD, 20892, USA.
Rayann AtwayLaboratory of Genitourinary Cancer Pathogenesis, National Cancer Institute, NIH, Bethesda, MD, 20892, USA.
Elizabeth D WaltonLaboratory of Genitourinary Cancer Pathogenesis, National Cancer Institute, NIH, Bethesda, MD, 20892, USA.
Berkley E GryderGenetics Branch, National Cancer Institute, NIH, Bethesda, MD, 20892, USA.ORCID http://orcid.org/0000-0003-0130-2302
Brian J CapaldoLaboratory of Genitourinary Cancer Pathogenesis, National Cancer Institute, NIH, Bethesda, MD, 20892, USA.
Huihui YeDepartment of Pathology, Beth Israel Deaconess Medical Center, Boston, MA, 02215, USA.
Adam G SowalskyLaboratory of Genitourinary Cancer Pathogenesis, National Cancer Institute, NIH, Bethesda, MD, 20892, USA. adam.sowalsky@nih.gov.ORCID http://orcid.org/0000-0003-2760-1853
National Cancer Institute · USBeth Israel Deaconess Medical Center · US

Funding

Laboratory of Genitourinary Cancer Pathogenesis Microscopy Core FacilityZICBC010947 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI LAKE, ROSS · 2009 to 2025
$11.0M
Molecular alterations driving the development of primary prostate cancersZIABC011679 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI SOWALSKY, ADAM · 2016 to 2025
$6.9M
Intramural NIH HHS Z99 CA999999Intramural NIH HHS ZIA BC011679
6 · The paper itself

Abstract

Localized prostate cancer develops very slowly in most men, with the androgen receptor (AR) and MYC transcription factors amongst the most well-characterized drivers of prostate tumorigenesis. Canonically, MYC up-regulation in luminal prostate cancer cells functions to oppose the terminally differentiating effects of AR. However, the effects of MYC up-regulation are pleiotropic and inconsistent with a poorly proliferative phenotype. Here we show that increased MYC expression and activity are associated with the down-regulation of MEIS1, a HOX-family transcription factor. Using RNA-seq to profile a series of human prostate cancer specimens laser capture microdissected on the basis of MYC immunohistochemistry, MYC activity, and MEIS1 expression were inversely correlated. Knockdown of MYC expression in prostate cancer cells increased the expression of MEIS1 and increased the occupancy of MYC at the MEIS1 locus. Finally, we show in laser capture microdissected human prostate cancer samples and the prostate TCGA cohort that MEIS1 expression is inversely proportional to AR activity as well as HOXB13, a known interacting protein of both AR and MEIS1. Collectively, our data demonstrate that elevated MYC in a subset of primary prostate cancers functions in a negative role in regulating MEIS1 expression, and that this down-regulation may contribute to MYC-driven development and progression.

Indexed as

Cell Line, TumorDown-RegulationGene Expression ProfilingGene Expression Regulation, NeoplasticHomeodomain ProteinsHumansMaleMyeloid Ecotropic Viral Integration Site 1 ProteinProstatic NeoplasmsProto-Oncogene Proteins c-mycReceptors, AndrogenHomeodomain ProteinsHOXB13 protein, humanMYC protein, humanMyeloid Ecotropic Viral Integration Site 1 ProteinProto-Oncogene Proteins c-mycReceptors, Androgen

Identifiers

PMID32681068
PMCPMC7441006
OpenAlexW3042738805

What OpenQuestion holds

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Registered trials

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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.