Evidence map›Paper›PMID 28881646›Full record

ArticleOncotarget2017

Modeling African American prostate adenocarcinoma by inducing defined genetic alterations in organoids.

Kenji Unno, Meejeon Roh, Young A Yoo, Yousef Al-Shraideh, Lu Wang, Larisa Nonn, Sarki A Abdulkadir

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

13 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Article
  3. Current concepts in tumour-derived organoids.British journal of cancer · 2020
    Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. CytochromeCancer research · 2019
    Article
  11. Anaplastic Lymphoma Kinase Mutation (Clinical cancer research : an official journal of the American Association for Cancer Research · 2018
    Article
  12. Article
  13. 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 1 country.

Kenji UnnoDepartment of Urology, Northwestern University Feinberg School of Medicine, Chicago, IL 60611, USA.
Meejeon RohDepartment of Urology, Northwestern University Feinberg School of Medicine, Chicago, IL 60611, USA.
Young A YooDepartment of Urology, Northwestern University Feinberg School of Medicine, Chicago, IL 60611, USA.
Yousef Al-ShraidehDepartment of Urology, Northwestern University Feinberg School of Medicine, Chicago, IL 60611, USA.
Lu WangDepartment of Pathology, Northwestern University Feinberg School of Medicine, Chicago, IL 60611, USA.
Larisa NonnDepartment of Pathology, University of Illinois at Chicago, Chicago, IL 60612, USA.
Sarki A AbdulkadirDepartment of Urology, Northwestern University Feinberg School of Medicine, Chicago, IL 60611, USA.
Northwestern University · USUniversity of Illinois Chicago · US

Funding

Targeting FOXA1-downstream pathways: a novel therapeutic strategy for castration-resistant prostate cancerP50CA180995 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI ABDULKADIR, SARKI A., HUSSAIN, MAHA H · 2015 to 2025
$19.9M
Research Education CoreU54CA202997 · NCI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI CIECIERSKI, CHRISTINA, FEINGLASS, JOSEPH M · 2015 to 2024
$13.8M
Research Education CoreU54CA203000 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI CIECIERSKI, CHRISTINA, FEINGLASS, JOSEPH M · 2015 to 2024
$12.4M
The Chicago Cancer Health Equity Collaborative (ChicagoCHEC)U54CA202995 · NCI · NORTHEASTERN ILLINOIS UNIVERSITY · PI CIECIERSKI, CHRISTINA · 2015 to 2024
$9.5M
Role of Oncogenic Kinase Pim-1 in Prostate CancerR01CA123484 · NCI · VANDERBILT UNIVERSITY · PI ABDULKADIR, SARKI A. · 2007 to 2017
$2.9M
Prostate Cancer Recurrence: models and mechanismsR01CA167966 · NCI · VANDERBILT UNIVERSITY · PI ABDULKADIR, SARKI A. · 2012 to 2016
$1.8M
NCI NIH HHS P50 CA180995NCI NIH HHS R01 CA123484NCI NIH HHS R01 CA167966NCI NIH HHS U54 CA202995NCI NIH HHS U54 CA202997NCI NIH HHS U54 CA203000
6 · The paper itself

Abstract

Genomic studies are rapidly identifying genetic alterations in human cancer, but functional validation of such alterations has been slow. Here, using human prostate cancer as a model, we have assessed the feasibility of engineering defined genetic alterations in well-known cancer driver genes to transform benign prostate epithelial organoids derived from African American men. Benign human prostate organoids were transduced with lentiviruses expressing MYC, shPTEN, shTP53 and AR, alone and in various combinations, to recapitulate prostate cancer development. Organoids expressing MYC, shPTEN, shTP53 and AR (denoted MPPA); MYC, shPTEN and shTP53 (MPP); or MYC (M) were significantly larger, had higher proliferation rates and demonstrated pathologically transformed morphology compared to organoids transduced with control lentivirus. Alterations in MYC, PTEN and TP53 also affected the rate of organoid basal-to-luminal differentiation

Indexed as

African Americancancer developmentmalignant transformationorganoid cultureprostate cancer

Identifiers

PMID28881646
PMCPMC5584247
OpenAlexW2606108784

What OpenQuestion holds

Textmetadata
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.