Sorafenib and Palbociclib Combination Regresses a Cisplatinum-resistant Osteosarcoma in a PDOX Mouse Model.


Journal

Anticancer research
ISSN: 1791-7530
Titre abrégé: Anticancer Res
Pays: Greece
ID NLM: 8102988

Informations de publication

Date de publication:
Aug 2019
Historique:
received: 06 06 2019
revised: 28 06 2019
accepted: 01 07 2019
entrez: 2 8 2019
pubmed: 2 8 2019
medline: 8 8 2019
Statut: ppublish

Résumé

Recurrent osteosarcoma is a recalcitrant disease; therefore, an improved strategy is urgently needed to provide therapy. In order to develop a novel strategy for this disease, our lab has developed a patient-derived orthotopic xenograft (PDOX) mouse model for osteosarcoma. The combination of sorafenib (SFN) and palbociclib (PAL) was shown to be effective of hepatocellular carcinoma. However, whether this combination is efficacious on osteosarcoma has not been reported. The aim of this study was to determine the efficacy of the SFN and PAL combination on a cisplatinum (CDDP)-resistant osteosarcoma PDOX model. Osteosarcoma PDOX models were randomly divided into five treatment groups: untreated-control, CDDP, SFN, PAL and the combination of SFN and PAL. Of these agents, the SFN-PAL combination significantly regressed tumor growth, and enhanced tumor necrosis with degenerative changes in the osteosarcoma PDOX. The SFN-PAL combination is an effective treatment strategy for osteosarcoma and therefore holds promise for clinical efficacy.

Sections du résumé

BACKGROUND/AIM OBJECTIVE
Recurrent osteosarcoma is a recalcitrant disease; therefore, an improved strategy is urgently needed to provide therapy. In order to develop a novel strategy for this disease, our lab has developed a patient-derived orthotopic xenograft (PDOX) mouse model for osteosarcoma. The combination of sorafenib (SFN) and palbociclib (PAL) was shown to be effective of hepatocellular carcinoma. However, whether this combination is efficacious on osteosarcoma has not been reported. The aim of this study was to determine the efficacy of the SFN and PAL combination on a cisplatinum (CDDP)-resistant osteosarcoma PDOX model.
MATERIALS AND METHODS METHODS
Osteosarcoma PDOX models were randomly divided into five treatment groups: untreated-control, CDDP, SFN, PAL and the combination of SFN and PAL.
RESULTS RESULTS
Of these agents, the SFN-PAL combination significantly regressed tumor growth, and enhanced tumor necrosis with degenerative changes in the osteosarcoma PDOX.
CONCLUSION CONCLUSIONS
The SFN-PAL combination is an effective treatment strategy for osteosarcoma and therefore holds promise for clinical efficacy.

Identifiants

pubmed: 31366491
pii: 39/8/4079
doi: 10.21873/anticanres.13565
doi:

Substances chimiques

Piperazines 0
Pyridines 0
Doxorubicin 80168379AG
Sorafenib 9ZOQ3TZI87
palbociclib G9ZF61LE7G
Cisplatin Q20Q21Q62J

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

4079-4084

Informations de copyright

Copyright© 2019, International Institute of Anticancer Research (Dr. George J. Delinasios), All rights reserved.

Auteurs

Takashi Higuchi (T)

AntiCancer, Inc., San Diego, CA, U.S.A.
Department of Surgery, University of California, San Diego, CA, U.S.A.
Department of Orthopedic Surgery, Kanazawa University, Kanazawa, Japan.

Norihiko Sugisawa (N)

AntiCancer, Inc., San Diego, CA, U.S.A.
Department of Surgery, University of California, San Diego, CA, U.S.A.

Kentaro Miyake (K)

AntiCancer, Inc., San Diego, CA, U.S.A.
Department of Surgery, University of California, San Diego, CA, U.S.A.

Hiromichi Oshiro (H)

AntiCancer, Inc., San Diego, CA, U.S.A.
Department of Surgery, University of California, San Diego, CA, U.S.A.

Norio Yamamoto (N)

Department of Orthopedic Surgery, Kanazawa University, Kanazawa, Japan.

Katsuhiro Hayashi (K)

Department of Orthopedic Surgery, Kanazawa University, Kanazawa, Japan.

Hiroaki Kimura (H)

Department of Orthopedic Surgery, Kanazawa University, Kanazawa, Japan.

Shinji Miwa (S)

Department of Orthopedic Surgery, Kanazawa University, Kanazawa, Japan.

Kentaro Igarashi (K)

Department of Orthopedic Surgery, Kanazawa University, Kanazawa, Japan.

Sant P Chawla (SP)

Sarcoma Oncology Center, Santa Monica, CA, U.S.A.

Michael Bouvet (M)

Department of Surgery, University of California, San Diego, CA, U.S.A.

Shree Ram Singh (SR)

Basic Research Laboratory, National Cancer Institute, Frederick, MD, U.S.A. all@anticancer.com singhshr@mail.nih.gov tsuchi@med.kanazawa-u.ac.jp.

Hiroyuki Tsuchiya (H)

Department of Orthopedic Surgery, Kanazawa University, Kanazawa, Japan all@anticancer.com singhshr@mail.nih.gov tsuchi@med.kanazawa-u.ac.jp.

Robert M Hoffman (RM)

AntiCancer, Inc., San Diego, CA, U.S.A. all@anticancer.com singhshr@mail.nih.gov tsuchi@med.kanazawa-u.ac.jp.
Department of Surgery, University of California, San Diego, CA, U.S.A.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH