Evidence map›Paper›PMID 31146720›Full record

ArticleBMC cancer2019

Lineage relationship between prostate adenocarcinoma and small cell carcinoma.

Adelle D Kanan, Eva Corey, Ricardo Z N Vêncio, Arjun Ishwar, Alvin Y Liu

Open access · goldAbstract read
In one paragraph

Article in BMC cancer, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.9field-weighted citation impact, top 24% 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

7 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Advances in combined neuroendocrine carcinoma of lung cancer.Pathology oncology research : POR · 2024
    Review
  5. Review
  6. Article
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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

5 authors at 3 institutions in 3 countries.

Adelle D KananDepartment of Urology, University of Washington, Box 358056, 850 Republican Street, Seattle, Washington, 98195-6100, USA. adellekanan@outlook.com.
Eva CoreyDepartment of Urology, University of Washington, Box 358056, 850 Republican Street, Seattle, Washington, 98195-6100, USA.
Ricardo Z N VêncioDepartment of Mathematics, University of Sao Paulo, 3900 Ave Bandeirantes, Vila Monte Alegre, Ribeirão Preto, 14040-900, Brazil.
Arjun IshwarThermo Fisher Scientific, 168 3rd Ave, Waltham, Massachutts, 02451, USA.
Alvin Y LiuDepartment of Urology, University of Washington, Box 358056, 850 Republican Street, Seattle, Washington, 98195-6100, USA.
University of Washington · USSophia Genetics (Switzerland) · CHUniversidade de São Paulo · BR

Funding

The Early Detection Research Network: Biomarker Developmental LaboratoriesU01CA111244 · NCI · UNIVERSITY OF WASHINGTON · PI LIU, ALVIN Y · 2004 to 2015
$4.1M
NCI NIH HHS U01 CA111244
6 · The paper itself

Abstract

backgroundProstate cancer displays different morphologies which, in turn, affect patient outcome. This fact prompted questions about the lineage relationship between differentiated, more treatable prostate adenocarcinoma and poorly differentiated, less treatable non-adenocarcinoma including small cell carcinoma, and the molecular mechanism underlying prostate cancer differentiation.

methodsNewly available non-adenocarcinoma/small cell carcinoma PDX LuCaP lines were analyzed for expression of stem cell transcription factors (scTF) LIN28A, NANOG, POU5F1, SOX2, which are responsible for reprogramming or de-differentiation. cDNA of these genes were cloned from small cell carcinoma LuCaP 145.1 into expression vectors to determine if they could function in reprogramming.

resultsExpression of scTF was detected in small cell carcinoma LuCaP 93, 145.1, 145.2, and non-adenocarcinoma LuCaP 173.1, 173.2A. Transfection of scTF from LuCaP 145.1 altered the gene expression of prostate non-small cell carcinoma cells, as well as fibroblasts. The resultant cells grew in stem-like colonies. Of note was a 10-fold lower expression of B2M in the transfected cells. Low B2M was also characteristic of LuCaP 145.1. Conversely, B2M was increased when stem cells were induced to differentiate.

conclusionsThis work suggested a pathway in the emergence of non-adenocarcinoma/small cell carcinoma from adenocarcinoma through activation of scTF genes that produced cancer de-differentiation.

Indexed as

Adenocarcinomabeta 2-MicroglobulinCarcinoma, Small CellCell DedifferentiationCell LineCell LineageGene Expression ProfilingGene Expression Regulation, NeoplasticHumansMaleNanog Homeobox ProteinNeoplastic Stem CellsOctamer Transcription Factor-3Prostatic NeoplasmsRNA-Binding ProteinsSOXB1 Transcription FactorsB2M protein, humanbeta 2-MicroglobulinLIN28B protein, humanNanog Homeobox ProteinNANOG protein, humanOctamer Transcription Factor-3POU5F1 protein, humanRNA-Binding ProteinsSOX2 protein, humanSOXB1 Transcription FactorsCancer de-differentiationReprogrammingSmall cell carcinomaStem cell factors

Identifiers

PMID31146720
PMCPMC6543672
OpenAlexW2947264982

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.