Evidence map›Paper›PMID 32429558›Full record

ArticleCancers2020

Proteomic Tissue-Based Classifier for Early Prediction of Prostate Cancer Progression.

Yuqian Gao, Yi-Ting Wang, Yongmei Chen, Hui Wang, Denise Young, Tujin Shi, Yingjie Song, Athena A Schepmoes, Claire Kuo, Thomas L Fillmore and 12 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.0field-weighted citation impact, top 20% 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

11 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Prostate cancer stem cells and their targeted therapies.Frontiers in cell and developmental biology · 2024
    Review
  6. Review
  7. Review
  8. Article
  9. Review
  10. Prostate Cancer Biomarker Development: National Cancer Institute's Early Detection Research Network Prostate Cancer Collaborative Group Review.Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology · 2020
    Review
  11. 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

22 authors at 4 institutions in 1 country.

Yuqian GaoBiological Sciences Division, Pacific Northwest National Laboratory, Richland, WA 99354, USA.ORCID 0000-0003-1646-4515
Yi-Ting WangBiological Sciences Division, Pacific Northwest National Laboratory, Richland, WA 99354, USA.ORCID 0000-0001-7509-2016
Yongmei ChenHenry M. Jackson Foundation for the Advancement of Military Medicine, Bethesda, MD 20817, USA.
Hui WangBiological Sciences Division, Pacific Northwest National Laboratory, Richland, WA 99354, USA.
Denise YoungHenry M. Jackson Foundation for the Advancement of Military Medicine, Bethesda, MD 20817, USA.
Tujin ShiBiological Sciences Division, Pacific Northwest National Laboratory, Richland, WA 99354, USA.
Yingjie SongHenry M. Jackson Foundation for the Advancement of Military Medicine, Bethesda, MD 20817, USA.
Athena A SchepmoesBiological Sciences Division, Pacific Northwest National Laboratory, Richland, WA 99354, USA.
Claire KuoHenry M. Jackson Foundation for the Advancement of Military Medicine, Bethesda, MD 20817, USA.ORCID 0000-0002-0777-7475
Thomas L FillmoreBiological Sciences Division, Pacific Northwest National Laboratory, Richland, WA 99354, USA.
Wei-Jun QianBiological Sciences Division, Pacific Northwest National Laboratory, Richland, WA 99354, USA.ORCID 0000-0002-5393-2827
Richard D SmithBiological Sciences Division, Pacific Northwest National Laboratory, Richland, WA 99354, USA.ORCID 0000-0002-2381-2349
Sudhir SrivastavaCancer Biomarkers Research Group, Division of Cancer Prevention, National Cancer Institute, Bethesda, MD 20892, USA.
Jacob KaganCancer Biomarkers Research Group, Division of Cancer Prevention, National Cancer Institute, Bethesda, MD 20892, USA.
Albert DobiHenry M. Jackson Foundation for the Advancement of Military Medicine, Bethesda, MD 20817, USA.
Isabell A SesterhennJoint Pathology Center, Silver Spring, MD 20910, USA.
Inger L RosnerCenter for Prostate Disease Research, John P. Murtha Cancer Center Research Program, Department of Surgery, Uniformed Services University of the Health Sciences and Walter Reed National Military Medical Center, Bethesda, MD 20814, USA.
Gyorgy PetrovicsHenry M. Jackson Foundation for the Advancement of Military Medicine, Bethesda, MD 20817, USA.
Karin D RodlandBiological Sciences Division, Pacific Northwest National Laboratory, Richland, WA 99354, USA.
Shiv SrivastavaCenter for Prostate Disease Research, John P. Murtha Cancer Center Research Program, Department of Surgery, Uniformed Services University of the Health Sciences and Walter Reed National Military Medical Center, Bethesda, MD 20814, USA.
Jennifer CullenHenry M. Jackson Foundation for the Advancement of Military Medicine, Bethesda, MD 20817, USA.
Tao LiuBiological Sciences Division, Pacific Northwest National Laboratory, Richland, WA 99354, USA.ORCID 0000-0001-9529-6550
Pacific Northwest National Laboratory · USHenry M. Jackson Foundation · USUniformed Services University of the Health Sciences · USNational Cancer Institute · US

Funding

Equipment Supplement Request for a Research Resource for Ultra-sensitive High Throughput ProteomicsP41GM103493 · NIGMS · BATTELLE PACIFIC NORTHWEST LABORATORIES · PI SMITH, RICHARD D · 2012 to 2022
$22.6M
CANCER AND LEUKEMIA GROUP BU10CA012011 · NCI · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI ELLISON, ROSE R. · 1985 to 1987
–
NCI NIH HHS ACN15006-001, ACN12011-001NIGMS NIH HHS P41 GM103493
6 · The paper itself

Abstract

Although ~40% of screen-detected prostate cancers (PCa) are indolent, advanced-stage PCa is a lethal disease with 5-year survival rates around 29%. Identification of biomarkers for early detection of aggressive disease is a key challenge. Starting with 52 candidate biomarkers, selected from existing PCa genomics datasets and known PCa driver genes, we used targeted mass spectrometry to quantify proteins that significantly differed in primary tumors from PCa patients treated with radical prostatectomy (RP) across three study outcomes: (i) metastasis ≥1-year post-RP, (ii) biochemical recurrence ≥1-year post-RP, and (iii) no progression after ≥10 years post-RP. Sixteen proteins that differed significantly in an initial set of 105 samples were evaluated in the entire cohort (n = 338). A five-protein classifier which combined FOLH1, KLK3, TGFB1, SPARC, and CAMKK2 with existing clinical and pathological standard of care variables demonstrated significant improvement in predicting distant metastasis, achieving an area under the receiver-operating characteristic curve of 0.92 (0.86, 0.99,

Indexed as

biochemical recurrencebiomarkersearly detectionmetastasisprostate cancerproteomics

Identifiers

PMID32429558
PMCPMC7281161
OpenAlexW3024496996

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.