Potential Involvement of Jagged1 in Metastatic Progression of Human Breast Carcinomas. (6th January 2020)
- Record Type:
- Journal Article
- Title:
- Potential Involvement of Jagged1 in Metastatic Progression of Human Breast Carcinomas. (6th January 2020)
- Main Title:
- Potential Involvement of Jagged1 in Metastatic Progression of Human Breast Carcinomas
- Authors:
- Bednarz-Knoll, Natalia
Efstathiou, Antonia
Gotzhein, Frauke
Wikman, Harriet
Mueller, Volkmar
Kang, Yibin
Pantel, Klaus - Abstract:
- Abstract: BACKGROUND: Jagged1, the ligand of Notch, has been shown to be involved in formation of bone metastases in an experimental study. Here, clinical relevance of Jagged1 expression in tumor progression was assessed in human breast carcinomas. METHODS: Jagged1 expression was evaluated by immunohistochemistry in 228 tumor tissue samples and compared to clinicopathologic parameters and patients' outcomes. Furthermore, circulating tumor cells (CTCs) from peripheral blood of 100 unmatched metastatic cancer patients with progressive disease were enriched using Ficoll density gradient centrifugation and detected by pan-keratin/Jagged1/CD45 immunofluorescent staining. RESULTS: Jagged1 expression was detected in 50% of 228 tumors. Jagged1 expression was correlated with higher tumor grade ( P = 0.047), vascular invasion ( P = 0.026), luminal B subtype ( P = 0.016), overexpression of Her-2 ( P = 0.001), high Ki-67 expression ( P = 0.035), and aldehyde dehydrogenase 1 (ALDH1) positivity ( P = 0.013). Jagged 1 expression indicated shorter disease-free survival (DFS) ( P = 0.040) and metastasis-free survival ( P = 0.048) in lymph node–negative breast cancer for which it was the only independent predictor of DFS (multivariate analysis, P = 0.046). Tumors characterized by the strongest Jagged1 staining intensity (7.5% of cases) correlated with lymph node positivity ( P = 0.037), metastatic relapse ( P = 0.049), and higher number of disseminated tumor cells in bone marrow aspirates ( PAbstract: BACKGROUND: Jagged1, the ligand of Notch, has been shown to be involved in formation of bone metastases in an experimental study. Here, clinical relevance of Jagged1 expression in tumor progression was assessed in human breast carcinomas. METHODS: Jagged1 expression was evaluated by immunohistochemistry in 228 tumor tissue samples and compared to clinicopathologic parameters and patients' outcomes. Furthermore, circulating tumor cells (CTCs) from peripheral blood of 100 unmatched metastatic cancer patients with progressive disease were enriched using Ficoll density gradient centrifugation and detected by pan-keratin/Jagged1/CD45 immunofluorescent staining. RESULTS: Jagged1 expression was detected in 50% of 228 tumors. Jagged1 expression was correlated with higher tumor grade ( P = 0.047), vascular invasion ( P = 0.026), luminal B subtype ( P = 0.016), overexpression of Her-2 ( P = 0.001), high Ki-67 expression ( P = 0.035), and aldehyde dehydrogenase 1 (ALDH1) positivity ( P = 0.013). Jagged 1 expression indicated shorter disease-free survival (DFS) ( P = 0.040) and metastasis-free survival ( P = 0.048) in lymph node–negative breast cancer for which it was the only independent predictor of DFS (multivariate analysis, P = 0.046). Tumors characterized by the strongest Jagged1 staining intensity (7.5% of cases) correlated with lymph node positivity ( P = 0.037), metastatic relapse ( P = 0.049), and higher number of disseminated tumor cells in bone marrow aspirates ( P = 0.041). Twenty-one unmatched metastatic breast cancer patients with progressive disease were positive for CTCs, and 85.7% of the CTCs also expressed Jagged1. The presence of Jagged1(+) CTCs was significantly associated with shorter progression-free survival in patients treated with bisphosphonates ( P = 0.013). CONCLUSIONS: Jagged1 expression characterizes more aggressive breast carcinoma and might be involved in tumor cell dissemination, metastatic progression, and resistance to bone-targeting therapy in breast cancer patients. … (more)
- Is Part Of:
- Clinical chemistry. Volume 62:Number 2(2016)
- Journal:
- Clinical chemistry
- Issue:
- Volume 62:Number 2(2016)
- Issue Display:
- Volume 62, Issue 2 (2016)
- Year:
- 2016
- Volume:
- 62
- Issue:
- 2
- Issue Sort Value:
- 2016-0062-0002-0000
- Page Start:
- 378
- Page End:
- 386
- Publication Date:
- 2020-01-06
- Subjects:
- Clinical chemistry -- Periodicals
Pharmaceutical chemistry -- Periodicals
Biochemistry -- Periodicals
Biochimie -- Périodiques
Diagnostics biologiques -- Périodiques
Biochemistry
Clinical chemistry
Pharmaceutical chemistry
Biochemistry
Laboratory Techniques and Procedures
Klinische chemie
Periodicals
616.075605 - Journal URLs:
- http://www.oxfordjournals.org/ ↗
https://academic.oup.com/clinchem ↗
http://catalog.hathitrust.org/api/volumes/oclc/1554929.html ↗
http://www.clinchem.org/ ↗ - DOI:
- 10.1373/clinchem.2015.246686 ↗
- Languages:
- English
- ISSNs:
- 0009-9147
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 16220.xml