Development and characterization of a patient‑derived orthotopic xenograft of therapy‑resistant breast cancer.
HER2
biomarker
breast cancer
estrogen receptor‑α
patient‑derived orthotopic xenograft
progesterone receptor‑α
Journal
Oncology reports
ISSN: 1791-2431
Titre abrégé: Oncol Rep
Pays: Greece
ID NLM: 9422756
Informations de publication
Date de publication:
May 2023
May 2023
Historique:
received:
04
04
2022
accepted:
05
12
2022
medline:
3
4
2023
entrez:
31
3
2023
pubmed:
1
4
2023
Statut:
ppublish
Résumé
Numerous years of cell line‑based studies have enhanced the current understanding of cancer and its treatment. However, limited success has been achieved in treating hormone receptor‑positive, HER2‑negative metastatic breast cancers that are refractory to treatment. The majority of cancer cell lines are unsuitable for use as pre‑clinical models that mimic this critical and often fatal clinical type, since they are derived from treatment‑naive or non‑metastatic breast cancer cases. The aim of the present study was to develop and characterize patient‑derived orthotopic xenografts (PDOXs) from patients with endocrine hormone receptor‑positive, HER2‑negative metastatic breast cancer who had relapsed on therapy. A patient who progressed on endocrine hormone therapy provided her tumor via a biobank. This tumor was implanted in mice. It was then serially passaged by implanting PDOX tumor fragments into another set of mice to develop further generations of PDOXs. These tissues were characterized using various histological and biochemical techniques. Histological, immunofluorescence and western blot analyses indicated that the PDOX tumors retained a similar morphology, histology and subtype‑specific molecular features to that of the patient's tumor. The present study successfully established PDOXs of hormone‑resistant breast cancer and characterized them in comparison with those derived from the original breast cancer tissue of the patient. The data highlight the reliability and usefulness of PDOX models for studies of biomarker discovery and preclinical drug screening. The present study was registered with the clinical trial registry of India (CTRI; registration no. CTRI/2017/11/010553; registered on 17/11/2017).
Identifiants
pubmed: 36999625
doi: 10.3892/or.2023.8536
pii: 99
pmc: PMC10091080
doi:
pii:
Substances chimiques
Hormones
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Références
Breast Cancer Res. 2003;5(2):89-95
pubmed: 12631387
JCO Glob Oncol. 2020 Jul;6:1063-1075
pubmed: 32673076
Cancer Res. 2018 Oct 15;78(20):5958-5969
pubmed: 30154149
Ecancermedicalscience. 2012 Nov 14;6:ed16
pubmed: 24883085
Proc Natl Acad Sci U S A. 2011 Nov 15;108(46):18708-13
pubmed: 22068913
J Nucl Med. 2016 Feb;57 Suppl 1:60S-8S
pubmed: 26834104
Br J Cancer. 2020 Mar;122(5):601-602
pubmed: 31919403
Cancer Res. 2016 Aug 15;76(16):4619-26
pubmed: 27325646
Breast Cancer Res Treat. 2018 Jun;169(2):381-390
pubmed: 29392581
Int J Oncol. 2015 Jul;47(1):61-70
pubmed: 25963555
J Immunol. 1995 Jan 1;154(1):180-91
pubmed: 7995938
Cells. 2019 Aug 13;8(8):
pubmed: 31412684
J Exp Med. 1993 Jan 1;177(1):191-4
pubmed: 8418200
Cancer Cell Int. 2014 Feb 05;14(1):14
pubmed: 24502646
Cold Spring Harb Protoc. 2014 Jul 01;2014(7):694-708
pubmed: 24987146
J Proteome Res. 2015 Jul 2;14(7):2819-27
pubmed: 26055192
Oncotarget. 2016 Oct 4;7(40):66212-66225
pubmed: 27517155
World J Clin Oncol. 2022 Mar 24;13(3):209-218
pubmed: 35433294
Int J Cancer. 2021 May 1;148(9):2304-2312
pubmed: 33197273
Ann Oncol. 2012 Oct;23(10):2605-2612
pubmed: 22910840
Clin Breast Cancer. 2015 Feb;15(1):e55-62
pubmed: 25445418
Breast Cancer Res. 2019 Aug 28;21(1):98
pubmed: 31462307
Front Genet. 2019 Aug 13;10:738
pubmed: 31456818
Nat Rev Clin Oncol. 2012 Apr 17;9(6):338-50
pubmed: 22508028
Asia Pac J Clin Oncol. 2017 Aug;13(4):289-295
pubmed: 28181405
Cancer Res. 2008 Jan 1;68(1):152-61
pubmed: 18172307