Circulating Cellular Communication Network Factor 1 Protein as a Sensitive Liquid Biopsy Marker for Early Detection of Breast Cancer.


Journal

Clinical chemistry
ISSN: 1530-8561
Titre abrégé: Clin Chem
Pays: England
ID NLM: 9421549

Informations de publication

Date de publication:
01 02 2022
Historique:
received: 01 07 2021
accepted: 16 07 2021
pubmed: 31 8 2021
medline: 14 4 2022
entrez: 30 8 2021
Statut: ppublish

Résumé

Despite recent progress in liquid biopsy technologies, early blood-based detection of breast cancer is still a challenge. We analyzed secretion of the protein cellular communication network factor 1 (CCN1, formerly cysteine-rich angiogenic inducer 61) in breast cancer cell lines by an enzyme-linked immunosorbent assay (ELISA). Soluble CCN1 in the plasma (2.5 µL) of 544 patients with breast cancer and 427 healthy controls was analyzed by ELISA. The breast cancer samples were acquired at the time of primary diagnosis prior to neoadjuvant therapy or surgery. A classifier was established on a training cohort of patients with breast cancer and age-adapted healthy controls and further validated on an independent cohort comprising breast cancer patients and healthy controls. Samples from patients with benign breast diseases were investigated as additional controls. Samples from patients with acute heart diseases (n = 127) were investigated as noncancer controls. The diagnostic accuracy was determined by receiver operating characteristic using the parameters area under the curve, sensitivity, and specificity. CCN1 was frequently secreted by breast cancer cell lines into the extracellular space. Subsequent analysis of clinical blood samples from patients with breast cancer and age-adjusted healthy controls revealed an overall specificity of 99.0% and sensitivity of 80.0% for cancer detection. Remarkably, 81.5% of small T1 cancers were already CCN1-positive, while CCN1 concentrations in patients with benign breast lesions were below the threshold for breast cancer detection. Circulating CCN1 is a potentially novel blood biomarker for the detection of breast cancer at the earliest invasive stage.

Sections du résumé

BACKGROUND
Despite recent progress in liquid biopsy technologies, early blood-based detection of breast cancer is still a challenge.
METHODS
We analyzed secretion of the protein cellular communication network factor 1 (CCN1, formerly cysteine-rich angiogenic inducer 61) in breast cancer cell lines by an enzyme-linked immunosorbent assay (ELISA). Soluble CCN1 in the plasma (2.5 µL) of 544 patients with breast cancer and 427 healthy controls was analyzed by ELISA. The breast cancer samples were acquired at the time of primary diagnosis prior to neoadjuvant therapy or surgery. A classifier was established on a training cohort of patients with breast cancer and age-adapted healthy controls and further validated on an independent cohort comprising breast cancer patients and healthy controls. Samples from patients with benign breast diseases were investigated as additional controls. Samples from patients with acute heart diseases (n = 127) were investigated as noncancer controls. The diagnostic accuracy was determined by receiver operating characteristic using the parameters area under the curve, sensitivity, and specificity.
RESULTS
CCN1 was frequently secreted by breast cancer cell lines into the extracellular space. Subsequent analysis of clinical blood samples from patients with breast cancer and age-adjusted healthy controls revealed an overall specificity of 99.0% and sensitivity of 80.0% for cancer detection. Remarkably, 81.5% of small T1 cancers were already CCN1-positive, while CCN1 concentrations in patients with benign breast lesions were below the threshold for breast cancer detection.
CONCLUSIONS
Circulating CCN1 is a potentially novel blood biomarker for the detection of breast cancer at the earliest invasive stage.

Identifiants

pubmed: 34458901
pii: 6359437
doi: 10.1093/clinchem/hvab153
doi:

Substances chimiques

Biomarkers 0
Biomarkers, Tumor 0
Proteins 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

344-353

Subventions

Organisme : Stiftung für Pathobiochemie und Molekulare Diagnostik
Organisme : ERC Advanced Investigator Grant
ID : INJURMET (834974)
Organisme : Kastner
Organisme : German Center for Cardiovascular Disease (DZHK
ID : FKZ 81Z0710102
Organisme : Abbott Diagnostics
Organisme : Bayer
Organisme : Siemens
Organisme : Singulex
Organisme : Thermo Fischer outside the submitted work
Organisme : Novartis, Roche, Seagen, and Genentech
Organisme : MeritMedical, Mammotome, and Endomag outside the submitted work

Informations de copyright

© American Association for Clinical Chemistry 2021.

Auteurs

Kai Bartkowiak (K)

Department of Tumor Biology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

Isabel Heidrich (I)

Department of Tumor Biology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

Marcel Kwiatkowski (M)

Department of Functional Proteo-Metabolomics, Institute of Biochemistry, University of Innsbruck, Innsbruck, Austria.

Maggie Banys-Paluchowski (M)

Department of Gynecology and Obstetrics, University Hospital Schleswig-Holstein, Lübeck, Germany.
Department Working Group Gynecological Oncology, Medical Faculty, Heinrich-Heine-University Düsseldorf, Düsseldorf, Germany.

Antje Andreas (A)

Department of Tumor Biology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

Marcus Wurlitzer (M)

Department of Clinical Chemistry and Laboratory Medicine, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

Maria Geffken (M)

Department of Transfusion Medicine, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

Hannah Voß (H)

Department of Clinical Chemistry and Laboratory Medicine, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

Tanja Zeller (T)

Department of General and Interventional Cardiology, University Heart Center Hamburg -Eppendorf, Hamburg, Germany.
German Center of Cardiovascular Disease (DZHK), Partner Site Hamburg, Lübeck, Kiel, Hamburg, Germany.

Stefan Blankenberg (S)

Mildred Scheel Cancer Career Center HaTriCS4, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Department of Gynecology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

Sven Peine (S)

Department of Transfusion Medicine, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

Simon A Joosse (SA)

Department of Tumor Biology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Mildred Scheel Cancer Career Center HaTriCS4, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

Volkmar Müller (V)

Department of Gynecology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

Hartmut Schlüter (H)

Department of Clinical Chemistry and Laboratory Medicine, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

Leticia Oliveira-Ferrer (L)

Department of Gynecology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

Klaus Pantel (K)

Department of Tumor Biology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

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Classifications MeSH