Evidence map›Paper›PMID 30282979›Full record

ArticleScientific reports2018

CLIC1 and CLIC4 complement CA125 as a diagnostic biomarker panel for all subtypes of epithelial ovarian cancer.

Bipradeb Singha, Sandra L Harper, Aaron R Goldman, Benjamin G Bitler, Katherine M Aird, Mark E Borowsky, Mark G Cadungog, Qin Liu, Rugang Zhang, Stephanie Jean and 2 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
4.7field-weighted citation impact, top 5% 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

30 citing papers in PubMed, 45 citations in OpenAlex.

  1. Article
  2. Article
  3. Mechanistic Insights into Tumorigenesis from Serum Proteins.medRxiv : the preprint server for health sciences · 2025
    Article
  4. Review
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  7. Ion Channels and Personalized Medicine in Gynecological Cancers.Pharmaceuticals (Basel, Switzerland) · 2023
    Review
  8. Review
  9. Article
  10. Intracellular chloride channel 1 and tumor.American journal of cancer research · 2023
    Review
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. 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

12 authors at 4 institutions in 1 country.

Bipradeb SinghaMolecular and Cellular Oncogenesis Program, The Wistar Institute, Philadelphia, Pennsylvania, 19104, USA.
Sandra L HarperMolecular and Cellular Oncogenesis Program, The Wistar Institute, Philadelphia, Pennsylvania, 19104, USA.
Aaron R GoldmanMolecular and Cellular Oncogenesis Program, The Wistar Institute, Philadelphia, Pennsylvania, 19104, USA.
Benjamin G BitlerDepartment of Obstetrics and Gynecology, University of Colorado, Aurora, Colorado, 80045, USA.
Katherine M AirdDepartment of Cellular and Molecular Physiology, Penn State College of Medicine, Hershey, Pennsylvania, 17033, USA.
Mark E BorowskyHelen F. Graham Cancer Center & Research Institute, Newark, Delaware, 19713, USA.
Mark G CadungogHelen F. Graham Cancer Center & Research Institute, Newark, Delaware, 19713, USA.
Qin LiuMolecular and Cellular Oncogenesis Program, The Wistar Institute, Philadelphia, Pennsylvania, 19104, USA.ORCID http://orcid.org/0000-0001-9964-580X
Rugang ZhangGene Expression and Regulation Program, The Wistar Institute, Philadelphia, Pennsylvania, 19104, USA.ORCID http://orcid.org/0000-0002-7255-2360
Stephanie JeanHelen F. Graham Cancer Center & Research Institute, Newark, Delaware, 19713, USA.
Ronny DrapkinDepartment of Obstetrics and Gynecology, Ovarian Cancer Research Center, University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania, 19104, USA.
David W SpeicherMolecular and Cellular Oncogenesis Program, The Wistar Institute, Philadelphia, Pennsylvania, 19104, USA. speicher@wistar.org.
The Wistar Institute · USCancer Research Center · USPenn State Milton S. Hershey Medical Center · USUniversity of Colorado Anschutz Medical Campus · US

Funding

Tumor Microenvironment and MetastasisP30CA010815 · NCI · WISTAR INSTITUTE · PI Dario C Altieri · 1985 to 2026
$75.9M
TRAINING PROGRAM IN BASIC CANCER RESEARCHT32CA009171 · NCI · WISTAR INSTITUTE · PI Alessandro Gardini · 1985 to 2026
$15.3M
Identification of Ovarian Cancer Plasma BiomarkersR01CA131582 · NCI · WISTAR INSTITUTE · PI SPEICHER, DAVID W. · 2009 to 2018
$4.1M
Advancing Cancer Research through Comprehensive Proteomics and Metabolomics AnalysesR50CA221838 · NCI · WISTAR INSTITUTE · PI Hsin-Yao Tang · 2017 to 2026
$2.1M
Nucleotide Metabolism in Senescence and Platinum Resistance of Ovarian CancerR00CA194309 · NCI · PENNSYLVANIA STATE UNIV HERSHEY MED CTR · PI AIRD, KATHERINE MARIE · 2017 to 2019
$697k
Nucleotide Metabolism in Senescence and Platinum Resistance of Ovarian CancerK99CA194309 · NCI · WISTAR INSTITUTE · PI AIRD, KATHERINE MARIE · 2015 to 2016
$230k
Targeting Wnt signaling to overcome PARP inhibitor resistance in ovarian cancerK99CA194318 · NCI · WISTAR INSTITUTE · PI BITLER, BENJAMIN G · 2015 to 2016
$230k
NCI NIH HHS K99 CA194309NCI NIH HHS K99 CA194318NCI NIH HHS P30 CA010815NCI NIH HHS R00 CA194309NCI NIH HHS R01 CA131582NCI NIH HHS R50 CA221838NCI NIH HHS T32 CA009171
6 · The paper itself

Abstract

New plasma and tissue biomarkers of epithelial ovarian cancer (EOC) could improve early diagnosis and post-diagnosis clinical management. Here we investigated tissue staining and tissue secretion of CLIC1 and CLIC4 across EOC subtypes. CLIC1 and CLIC4 are two promising biomarkers we previously showed were elevated in EOC patient sera. Individually, CLIC1 or CLIC4 stained larger percentages of malignant tumors across all EOC subtypes compared with CA125, particularly early stage and mucinous tumors. CLIC4 also stained benign tumors but staining was limited to nuclei; whereas malignant tumors showed diffuse cellular staining of stromal and tumor cells. Both proteins were shed by all EOC subtypes tumors in short term organ culture at more consistent levels than CA125, supporting their potential as pan-subtype serum and tissue biomarkers. Elevated CLIC4 expression, but not CLIC1 expression, was a negative indicator of patient survival, and CLIC4 knockdown in cultured cells decreased cell proliferation and migration indicating a potential role in tumor progression. These results suggest CLIC1 and CLIC4 are promising serum and tissue biomarkers as well as potential therapeutic targets for all EOC subtypes. This justifies development of high throughput serum/plasma biomarker assays to evaluate utility of a biomarker panel consisting of CLIC1, CLIC4 and CA125.

Indexed as

AgedBiomarkers, TumorCA-125 AntigenCarcinoma, Ovarian EpithelialChloride ChannelsFemaleGene Expression Regulation, NeoplasticHumansMembrane ProteinsMiddle AgedBiomarkers, TumorCA-125 AntigenChloride ChannelsCLIC1 protein, humanCLIC4 protein, humanMembrane ProteinsMUC16 protein, human

Identifiers

PMID30282979
PMCPMC6170428
OpenAlexW2893973924

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Registered trials

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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.