Cyclin-dependent kinase 4/6 inhibitors suppress tumor growth in extramammary Paget's disease.
Aged
Aged, 80 and over
Animals
Cyclin D1
/ metabolism
Cyclin-Dependent Kinase 4
/ antagonists & inhibitors
Cyclin-Dependent Kinase 6
/ antagonists & inhibitors
Female
Humans
Male
Mice
Middle Aged
Paget Disease, Extramammary
/ drug therapy
Protein Kinase Inhibitors
/ therapeutic use
Skin
/ metabolism
Tumor Burden
/ drug effects
Xenograft Model Antitumor Assays
cancer
cyclin
cyclin-dependent kinase
extramammary Paget’s disease
patient-derived xenograft
Journal
Cancer science
ISSN: 1349-7006
Titre abrégé: Cancer Sci
Pays: England
ID NLM: 101168776
Informations de publication
Date de publication:
Feb 2022
Feb 2022
Historique:
revised:
20
11
2021
received:
17
10
2021
accepted:
30
11
2021
pubmed:
7
12
2021
medline:
12
2
2022
entrez:
6
12
2021
Statut:
ppublish
Résumé
Extramammary Paget's disease (EMPD) is a rare adnexal neoplasm commonly seen in the genital areas among the senior population. The prognosis of advanced EMPD is not favorable; thus, the development of potential treatments has long been sought. Cyclin-dependent kinase (CDK) 4/6 inhibitors such as abemaciclib and palbociclib have been proven effective against metastatic breast cancer; however, no studies have addressed CDK4/6 inhibitors as an EMPD treatment. We herein examine the efficacy of CDK4/6 inhibitors against an EMPD patient-derived xenograft (PDX) model. Abemaciclib (50 mg/kg/day) or palbociclib (120 mg/kg/day) was given orally to tumor-bearing NOD/Scid mice over a 3-week period. We also investigated the protein expression levels of CDK4/6 and cyclin D1 through immunohistochemical staining using EMPD clinical samples. Treatment with abemaciclib or palbociclib as a single agent was found to significantly suppress tumor growth in EMPD-PDX. The Ki-67-positive ratio of the treated EMPD-PDX tumors was significantly lower than that of the nontreated tumors. Clinically, the expression levels of CDK4 and cyclin D1 were significantly higher in the EMPD tumor cells than in the normal epidermis. Our results suggest that CDK4/6 inhibitors could be novel and potent therapeutics for the treatment of EMPD.
Identifiants
pubmed: 34866279
doi: 10.1111/cas.15234
pmc: PMC8819308
doi:
Substances chimiques
Protein Kinase Inhibitors
0
Cyclin D1
136601-57-5
Cyclin-Dependent Kinase 4
EC 2.7.11.22
Cyclin-Dependent Kinase 6
EC 2.7.11.22
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
802-807Subventions
Organisme : Japan Society for the Promotion of Science
ID : JP18K08259
Organisme : Japan Society for the Promotion of Science
ID : JP#21K1620101
Informations de copyright
© 2021 The Authors. Cancer Science published by John Wiley & Sons Australia, Ltd on behalf of Japanese Cancer Association.
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