A Triple-negative Matrix-producing Breast Carcinoma Patient-derived Orthotopic Xenograft (PDOX) Mouse Model Is Sensitive to Bevacizumab and Vinorelbine, Regressed by Eribulin and Resistant to Olaparib.
Adult
Animals
Bevacizumab
/ pharmacology
Cell Line, Tumor
Disease Models, Animal
Drug Resistance, Neoplasm
/ drug effects
Female
Furans
/ pharmacology
Humans
Ketones
/ pharmacology
Mice
Phthalazines
/ pharmacology
Piperazines
/ pharmacology
Triple Negative Breast Neoplasms
/ drug therapy
Vinorelbine
/ pharmacology
Xenograft Model Antitumor Assays
PDOX
TNBC
eribulin
matrix-producing breast carcinoma
nude mice
olaparib
patient-derived orthotopic xenograft
regression
resistance
triple-negative breast cancer
Journal
Anticancer research
ISSN: 1791-7530
Titre abrégé: Anticancer Res
Pays: Greece
ID NLM: 8102988
Informations de publication
Date de publication:
May 2020
May 2020
Historique:
received:
25
03
2020
revised:
06
04
2020
accepted:
14
04
2020
entrez:
6
5
2020
pubmed:
6
5
2020
medline:
19
5
2020
Statut:
ppublish
Résumé
Matrix-producing breast carcinoma (MPBC) is a rare and usually aggressive triple-negative breast cancer (TNBC). In this study, we determined drug sensitivity for a triple-negative MPBC, without BRCA mutations, in a patient-derived orthotopic xenograft (PDOX) model. The MPBC PDOX model was established in the left 2 The MPBC PDOX model was resistant to olaparib (p=0.22). The MPBC PDOX model treated with bevacizumab and vinorelbine showed significantly suppressed tumor growth compared to the untreated group (p=0.005 and 0.002, respectively). However, only eribulin regressed the tumor (p=0.0001). Eribulin was more effective than olaparib (p=0.0001), bevacizumab (p=0.0025) and vinorelbine (p=0.0061). Eribulin has clinical potential as treatment for triple-negative MPBC patients that are resistant to a PARP inhibitor such as olaparib.
Sections du résumé
BACKGROUND/AIM
OBJECTIVE
Matrix-producing breast carcinoma (MPBC) is a rare and usually aggressive triple-negative breast cancer (TNBC). In this study, we determined drug sensitivity for a triple-negative MPBC, without BRCA mutations, in a patient-derived orthotopic xenograft (PDOX) model.
MATERIALS AND METHODS
METHODS
The MPBC PDOX model was established in the left 2
RESULTS
RESULTS
The MPBC PDOX model was resistant to olaparib (p=0.22). The MPBC PDOX model treated with bevacizumab and vinorelbine showed significantly suppressed tumor growth compared to the untreated group (p=0.005 and 0.002, respectively). However, only eribulin regressed the tumor (p=0.0001). Eribulin was more effective than olaparib (p=0.0001), bevacizumab (p=0.0025) and vinorelbine (p=0.0061).
CONCLUSION
CONCLUSIONS
Eribulin has clinical potential as treatment for triple-negative MPBC patients that are resistant to a PARP inhibitor such as olaparib.
Identifiants
pubmed: 32366395
pii: 40/5/2509
doi: 10.21873/anticanres.14221
doi:
Substances chimiques
Furans
0
Ketones
0
Phthalazines
0
Piperazines
0
Bevacizumab
2S9ZZM9Q9V
eribulin
LR24G6354G
Vinorelbine
Q6C979R91Y
olaparib
WOH1JD9AR8
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
2509-2514Informations de copyright
Copyright© 2020, International Institute of Anticancer Research (Dr. George J. Delinasios), All rights reserved.