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Eribulin Regresses a Doxorubicin-resistant Dedifferentiated Liposarcoma in a Patient-derived Orthotopic Xenograft Mouse Model.

Authors :
Igarashi, Kentaro
Igarashi, Kentaro
Kawaguchi, Kei
Kiyuna, Tasuku
Miyake, Kentaro
Higuchi, Takashi
Yamamoto, Norio
Hayashi, Katsuhiro
Kimura, Hiroaki
Miwa, Shinji
Singh, Shree Ram
Tsuchiya, Hiroyuki
Hoffman, Robert M
Igarashi, Kentaro
Igarashi, Kentaro
Kawaguchi, Kei
Kiyuna, Tasuku
Miyake, Kentaro
Higuchi, Takashi
Yamamoto, Norio
Hayashi, Katsuhiro
Kimura, Hiroaki
Miwa, Shinji
Singh, Shree Ram
Tsuchiya, Hiroyuki
Hoffman, Robert M
Source :
Cancer genomics & proteomics; vol 17, iss 4, 351-358; 1109-6535
Publication Year :
2020

Abstract

Background/aimDedifferentiated liposarcoma (DDLPS) is recalcitrant type of sarcoma. DDLPS has a low survival rate with high recurrence and metastasis. In the present study, we evaluated the efficacy of several drugs against doxorubicin-resistant DDLPS in a patient-derived orthotopic xenograft (PDOX) model for precision oncology. To establish the PDOX model, a tumor from a patient who had recurrent high-grade DDLPS from the retroperitoneum was previously grown orthotopically in the retroperitoneum of nude mice.Materials and methodsWe randomized DDLPS PDOX models into 8 treatment groups when tumor volume became approximately 100 mm3: control, no treatment; G2, doxorubicin (DOX); G3, pazopanib (PAZ); G4, gemcitabine (GEM) combined with docetaxel (DOC); G5, trabectedin (YON); G6, temozolomide (TEM); G7, palbociclib (PAL); G8, eribulin (ERB). Tumor length and width were measured both at the beginning and at the end of treatment.ResultsAt the end of treatment (day 14), all treatments significantly inhibited DDLPS PDOX tumor growth compared to the untreated control, except DOX. ERB was significantly more effective and regressed tumor volume compared to other treatments on day 14 after initiation of treatment. No significant differences were found in the relative body weight on day 14 compared to day 0 in any group.ConclusionThe clinical potential of ERB against DDLPS is herein presented in a PDOX model.

Details

Database :
OAIster
Journal :
Cancer genomics & proteomics; vol 17, iss 4, 351-358; 1109-6535
Notes :
application/pdf, Cancer genomics & proteomics vol 17, iss 4, 351-358 1109-6535
Publication Type :
Electronic Resource
Accession number :
edsoai.on1391599559
Document Type :
Electronic Resource