Evidence map›Paper›PMID 32021935›Full record

ArticleHeliyon2020

TRA-1-60-positive/CD45

Claudia Schäfer, Yawen Ju, Youngbin Tak, Cesar Vazquez, Sangyoon J Han, Edwin Tan, Jerry W Shay, Mats Holmqvist, Gaudenz Danuser, William M Schopperle and 1 more

Open access · goldAbstract read
In one paragraph

Article in Heliyon, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.3field-weighted citation impact, top 45% 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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Review
  2. Review
  3. Selective ablation of TRA-1-60Theranostics · 2023
    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

11 authors at 3 institutions in 1 country.

Claudia SchäferDepartment of Cell Biology, University of Texas, Southwestern Medical Center, Dallas, TX, USA.
Yawen JuCureMeta, Boston, MA, USA.
Youngbin TakCureMeta, Boston, MA, USA.
Cesar VazquezGenitourinary Oncology, Beth Israel Deaconess Medical Center, Boston, MA, USA.
Sangyoon J HanDepartment of Cell Biology, University of Texas, Southwestern Medical Center, Dallas, TX, USA.
Edwin TanCureMeta, Boston, MA, USA.
Jerry W ShayDepartment of Cell Biology, University of Texas, Southwestern Medical Center, Dallas, TX, USA.
Mats HolmqvistCureMeta, Boston, MA, USA.
Gaudenz DanuserDepartment of Cell Biology, University of Texas, Southwestern Medical Center, Dallas, TX, USA.
William M SchopperleCureMeta, Boston, MA, USA.
Glenn BubleyGenitourinary Oncology, Beth Israel Deaconess Medical Center, Boston, MA, USA.
The University of Texas Southwestern Medical Center · USBeth Israel Deaconess Medical Center · USMichigan Technological University · US

Funding

Nascent Adhesion-Based Mechano-transmission for Extracellular Matrix Stiffness SensingR15GM135806 · NIGMS · MICHIGAN TECHNOLOGICAL UNIVERSITY · PI HAN, SANGYOON JOSHUA · 2019 to 2024
$964k
NIGMS NIH HHS R15 GM135806
6 · The paper itself

Abstract

purposeOver 90% of all cancer related deaths are due to metastasis. However, current diagnostic tools can't reliably discriminate between invasive and localized cancers. PATIENTS AND

methodsIn this proof-of-concept study, we employed the embryonic stem cell marker TRA-1-60 (TRA+) to identify TRA + cells within the blood of prostate cancer patients and searched for TRA + cells in men with metastatic and localized cancers. We isolated whole peripheral blood mononuclear cells from 26 metastatic prostate cancer patients, from 13 patients with localized prostate cancer and from 17 healthy controls. Cells were stained for DAPI, CD45 and TRA + by immunofluorescence and imaged by epi-fluorescence microscopy. Imaged-based software was used both to identify TRA + cells, and to analyze CD45 levels in TRA+ and negative cells.

resultsWe found high numbers of TRA + cells within the blood of metastatic cancer patients, whereas healthy individuals or men with localized prostate cancer showed none or very low numbers of TRA + cells. Further analysis of the CD45 levels of TRA + cells revealed a small population of TRA + cells with almost undetectable CD45 levels that were found frequently in metastatic prostate cancer patients. By excluding CD45 positive cells from the TRA + cell pool, we were able to refine the assay to be highly specific in identifying men with metastatic disease. In fact, the difference of CD45 levels between TRA+ and negative cells was a robust measure to distinguish between men with localized and metastatic prostate cancers in this small patient cohort.

conclusionsThe data suggest that metastatic prostate cancer patient have significant numbers of TRA+/CD45

Indexed as

CancerCancer researchDiagnosticsEmbryonic stem cellsMetastasisOncologyTRA-1-60

Identifiers

PMID32021935
PMCPMC6994489
OpenAlexW3001653743

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.