Evidence map›Paper›PMID 29718670›Full record

ArticleJournal of proteome research2018

Evaluation of NCI-7 Cell Line Panel as a Reference Material for Clinical Proteomics.

David J Clark, Yingwei Hu, William Bocik, Lijun Chen, Michael Schnaubelt, Rhonda Roberts, Punit Shah, Gordon Whiteley, Hui Zhang

Abstract read
In one paragraph

Article in Journal of proteome research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
–field-weighted citation impact
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

22 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Genesis and regulation of C-terminal cyclic imides from protein damage.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

9 authors.

David J ClarkDepartment of Pathology , Johns Hopkins University School of Medicine , Baltimore , Maryland 21205 , United States.ORCID 0000-0003-0527-8469
Yingwei HuDepartment of Pathology , Johns Hopkins University School of Medicine , Baltimore , Maryland 21205 , United States.ORCID 0000-0002-4629-0985
William BocikAntibody Characterization Laboratory, Cancer Research Technology Program , Frederick National Laboratory for Cancer Research , Frederick , Maryland 21701 , United States.
Lijun ChenDepartment of Pathology , Johns Hopkins University School of Medicine , Baltimore , Maryland 21205 , United States.
Michael SchnaubeltDepartment of Pathology , Johns Hopkins University School of Medicine , Baltimore , Maryland 21205 , United States.
Rhonda RobertsAntibody Characterization Laboratory, Cancer Research Technology Program , Frederick National Laboratory for Cancer Research , Frederick , Maryland 21701 , United States.
Punit ShahDepartment of Pathology , Johns Hopkins University School of Medicine , Baltimore , Maryland 21205 , United States.
Gordon WhiteleyAntibody Characterization Laboratory, Cancer Research Technology Program , Frederick National Laboratory for Cancer Research , Frederick , Maryland 21701 , United States.
Hui ZhangDepartment of Pathology , Johns Hopkins University School of Medicine , Baltimore , Maryland 21205 , United States.

Funding

The Comprehensive Proteome Characterization Center at Johns Hopkins: High Precision Discovery and Confirmation of Genoproteomic TargetsU24CA210985 · NCI · JOHNS HOPKINS UNIVERSITY · PI CHAN, DANIEL WANYUI, ZHANG, HUI · 2016 to 2020
$5.3M
NCI NIH HHS U24 CA210985
6 · The paper itself

Abstract

Reference materials are vital to benchmarking the reproducibility of clinical tests and essential for monitoring laboratory performance for clinical proteomics. The reference material utilized for mass spectrometric analysis of the human proteome would ideally contain enough proteins to be suitably representative of the human proteome, as well as exhibit a stable protein composition in different batches of sample regeneration. Previously, The Clinical Proteomic Tumor Analysis Consortium (CPTAC) utilized a PDX-derived comparative reference (CompRef) materials for the longitudinal assessment of proteomic performance; however, inherent drawbacks of PDX-derived material, including extended time needed to grow tumors and high level of expertise needed, have resulted in efforts to identify a new source of CompRef material. In this study, we examined the utility of using a panel of seven cancer cell lines, NCI-7 Cell Line Panel, as a reference material for mass spectrometric analysis of human proteome. Our results showed that not only is the NCI-7 material suitable for benchmarking laboratory sample preparation methods, but also NCI-7 sample generation is highly reproducible at both the global and phosphoprotein levels. In addition, the predicted genomic and experimental coverage of the NCI-7 proteome suggests the NCI-7 material may also have applications as a universal standard proteomic reference.

Indexed as

BenchmarkingCell Line, TumorHumansMass SpectrometryProteomeProteomicsReproducibility of ResultsProteomeclinical proteomicsmass spectrometryproteomics reference material

Identifiers

PMID29718670
PMCPMC6670293

What OpenQuestion holds

Textmetadata
LicenceTDM
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.