Evidence map›Paper›PMID 27775025›Full record

ArticleScientific reports2016

Basal Tumor Cell Isolation and Patient-Derived Xenograft Engraftment Identify High-Risk Clinical Bladder Cancers.

K B Skowron, S P Pitroda, J P Namm, O Balogun, M A Beckett, M L Zenner, O Fayanju, X Huang, C Fernandez, W Zheng and 7 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.9field-weighted citation impact, top 22% 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

10 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. Frontiers in oncology · 2022
    Article
  7. Article
  8. Review
  9. Review
  10. Review
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

17 authors at 1 institution in 1 country.

K B SkowronUniversity of Chicago Medicine, Dept. of Surgery, Chicago, IL, USA.
S P PitrodaUniversity of Chicago Medicine, Dept. of Radiation and Cellular Oncology, Chicago, IL, USA.
J P NammUniversity of Chicago Medicine, Dept. of Surgery, Chicago, IL, USA.
O BalogunUniversity of Chicago Medicine, Dept. of Radiation and Cellular Oncology, Chicago, IL, USA.
M A BeckettUniversity of Chicago Medicine, Dept. of Radiation and Cellular Oncology, Chicago, IL, USA.
M L ZennerUniversity of Chicago Medicine, Dept. of Radiation and Cellular Oncology, Chicago, IL, USA.
O FayanjuUniversity of Chicago Medicine, Dept. of Radiation and Cellular Oncology, Chicago, IL, USA.
X HuangUniversity of Chicago Medicine, Dept. of Radiation and Cellular Oncology, Chicago, IL, USA.
C FernandezUniversity of Chicago Medicine, Dept. of Radiation and Cellular Oncology, Chicago, IL, USA.
W ZhengUniversity of Chicago Medicine, Dept. of Radiation and Cellular Oncology, Chicago, IL, USA.
G QiaoUniversity of Chicago Medicine, Dept. of Radiation and Cellular Oncology, Chicago, IL, USA.
R ChinUniversity of Chicago Medicine, Dept. of Radiation and Cellular Oncology, Chicago, IL, USA.
S J KronUniversity of Chicago, Dept. of Molecular Genetics and Cell Biology, Chicago, IL, USA.
N N KhodarevUniversity of Chicago Medicine, Dept. of Radiation and Cellular Oncology, Chicago, IL, USA.
M C PosnerUniversity of Chicago Medicine, Dept. of Surgery, Chicago, IL, USA.
G D SteinbergUniversity of Chicago Medicine, Dept. of Surgery, Chicago, IL, USA.
R R WeichselbaumUniversity of Chicago Medicine, Dept. of Radiation and Cellular Oncology, Chicago, IL, USA.
University of Chicago · US

Funding

Re-Engineering Translational Research at the University of ChicagoUL1TR000430 · NCATS · UNIVERSITY OF CHICAGO · PI SOLWAY, JULIAN · 2012 to 2016
$20.2M
Radiation response within the tumor microenvironmentR01CA164492 · NCI · UNIVERSITY OF CHICAGO · PI KRON, STEPHEN J. · 2011 to 2015
$4.8M
PARP Inhibition To Enhance Induction for Head and Neck CancerR01CA176843 · NCI · UNIVERSITY OF CHICAGO · PI KRON, STEPHEN J. · 2013 to 2016
$1.3M
NCATS NIH HHS UL1 TR000430NCI NIH HHS R01 CA164492NCI NIH HHS R01 CA176843
6 · The paper itself

Abstract

Strategies to identify tumors at highest risk for treatment failure are currently under investigation for patients with bladder cancer. We demonstrate that flow cytometric detection of poorly differentiated basal tumor cells (BTCs), as defined by the co-expression of CD90, CD44 and CD49f, directly from patients with early stage tumors (T1-T2 and N0) and patient-derived xenograft (PDX) engraftment in locally advanced tumors (T3-T4 or N+) predict poor prognosis in patients with bladder cancer. Comparative transcriptomic analysis of bladder tumor cells isolated from PDXs indicates unique patterns of gene expression during bladder tumor cell differentiation. We found cell division cycle 25C (CDC25C) overexpression in poorly differentiated BTCs and determined that CDC25C expression predicts adverse survival independent of standard clinical and pathologic features in bladder cancer patients. Taken together, our findings support the utility of BTCs and bladder cancer PDX models in the discovery of novel molecular targets and predictive biomarkers for personalizing oncology care for patients.

Indexed as

AgedAnimalsBiomarkers, Tumorcdc25 PhosphatasesCell DifferentiationFemaleFlow CytometryGene Expression Regulation, NeoplasticHumansMaleMice, SCIDMiddle AgedPrognosisProspective StudiesUrinary Bladder NeoplasmsXenograft Model Antitumor AssaysBiomarkers, TumorCDC25C protein, humancdc25 Phosphatases

Identifiers

PMID27775025
PMCPMC5075783
OpenAlexW2534121389

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.