Blood endocan as a biomarker for breast cancer recurrence.

Endocan animal models biomarker clinical study recurrence

Journal

Cancer biomarkers : section A of Disease markers
ISSN: 1875-8592
Titre abrégé: Cancer Biomark
Pays: Netherlands
ID NLM: 101256509

Informations de publication

Date de publication:
23 Aug 2024
Historique:
medline: 27 9 2024
pubmed: 27 9 2024
entrez: 27 9 2024
Statut: aheadofprint

Résumé

Endocan was reported to affect breast cancer patients negatively and was able to be detected from patients' blood. This study aimed to investigate if the measurement of blood endocan in breast cancer patients with high ESM1 expression could be an effective tool to detect postoperative recurrence compared with existing tumor markers. Blood was collected before and after the tumor resection from the mouse models of breast cancer, and endocan levels were measured while visualizing metastatic recurrence with noninvasive luminescence imaging. In clinical settings, blood was withdrawn from 16 breast cancer patients before and after the tumor resection, and the effect of lumpectomy on blood endocan level was evaluated. Additionally, the blood endocan from 20 patients diagnosed with postoperative recurrence was measured, and their positivity rate for endocan was compared with that for serum carcinoembryonic antigen (CEA) or cancer antigen 15-3 (CA15-3). Our preclinical and clinical experiments revealed that blood endocan levels reflected tumor burden. Furthermore, over 60% of patients suffering from postoperative recurrence who tested negative for CEA or CA15-3 were positive for endocan. Our results support the clinical significance of endocan in breast cancer patients for detecting breast cancer recurrence.

Sections du résumé

BACKGROUND UNASSIGNED
Endocan was reported to affect breast cancer patients negatively and was able to be detected from patients' blood.
OBJECTIVE UNASSIGNED
This study aimed to investigate if the measurement of blood endocan in breast cancer patients with high ESM1 expression could be an effective tool to detect postoperative recurrence compared with existing tumor markers.
METHODS UNASSIGNED
Blood was collected before and after the tumor resection from the mouse models of breast cancer, and endocan levels were measured while visualizing metastatic recurrence with noninvasive luminescence imaging. In clinical settings, blood was withdrawn from 16 breast cancer patients before and after the tumor resection, and the effect of lumpectomy on blood endocan level was evaluated. Additionally, the blood endocan from 20 patients diagnosed with postoperative recurrence was measured, and their positivity rate for endocan was compared with that for serum carcinoembryonic antigen (CEA) or cancer antigen 15-3 (CA15-3).
RESULTS UNASSIGNED
Our preclinical and clinical experiments revealed that blood endocan levels reflected tumor burden. Furthermore, over 60% of patients suffering from postoperative recurrence who tested negative for CEA or CA15-3 were positive for endocan.
CONCLUSIONS UNASSIGNED
Our results support the clinical significance of endocan in breast cancer patients for detecting breast cancer recurrence.

Identifiants

pubmed: 39331092
pii: CBM240034
doi: 10.3233/CBM-240034
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Auteurs

Kentaro Daiki (K)

Laboratory for Bioanalysis and Onco-Pharmaceutics, Hoshi University School of Pharmacy and Pharmaceutical Sciences, Tokyo, Japan.

Yoko Kanada (Y)

Department of Breast Surgical Oncology, Tokyo Rosai Hospital, Tokyo, Japan.

Aya Nagata (A)

Department of Breast Surgical Oncology, Showa University Fujigaoka Hospital, Yokohama, Japan.

Kanae Taruno (K)

Institute for Clinical Genetics and Genomics, Showa University, Tokyo, Japan.

Katsuhide Igarashi (K)

Laboratory of Biofunctional Science, Hoshi University School of Pharmacy and Pharmaceutical Sciences, Tokyo, Japan.

Toshiko Yamochi (T)

Department of Pathology, Showa University School of Medicine, Tokyo, Japan.

Hirotaka Ota (H)

Department of Pathology, Showa University School of Medicine, Tokyo, Japan.

Fumiaki Sato (F)

Laboratory for Bioanalysis and Onco-Pharmaceutics, Hoshi University School of Pharmacy and Pharmaceutical Sciences, Tokyo, Japan.

Seigo Nakamura (S)

Institute for Clinical Genetics and Genomics, Showa University, Tokyo, Japan.

Yoshinori Kato (Y)

Laboratory for Bioanalysis and Onco-Pharmaceutics, Hoshi University School of Pharmacy and Pharmaceutical Sciences, Tokyo, Japan.

Classifications MeSH