| Literature DB >> 31200257 |
Kentaro Miyake1, Takashi Higuchi2, Hiromichi Oshiro2, Zhiying Zhang2, Norihiko Sugisawa2, Jun Ho Park2, Sahar Razmjooei2, Yuki Katsuya2, Maryam Barangi2, Yunfeng Li3, Scott D Nelson3, Takashi Murakami4, Yuki Homma4, Yukihiko Hiroshima4, Ryusei Matsuyama4, Michael Bouvet5, Sant P Chawla6, Shree Ram Singh7, Itaru Endo8, Robert M Hoffman9.
Abstract
Liposarcoma (LS) is a chemotherapy-resistant disease. The aim of the present study was to find precise therapy for a recurrent dedifferentiated liposarcoma (DDLS) in a patient-derived orthotopic xenograft (PDOX) model. The DDLS PDOX models were established orthotopically in the right inguinal area of nude mice. The DDLS PDOX models were randomized into five groups: untreated; doxorubicin (DOX); gemcitabine (GEM) combined with docetaxel (DOC); pazopanib (PAZ); and yondelis (YON). On day 15, all mice were sacrificed. Measurement of tumor volume and body weight were done two times a week. The DDLS PDOX was resistant to DOX (P > 0.184). YON suppressed tumor growth significantly compared to control group (P < 0.027). However, only GEM combined with DOC arrested the tumor growth (P < 0.001). These findings suggest that GEM combined with DOC has clinical potential for this and possibly other DDLS patients.Entities:
Keywords: Docetaxel; Gemcitabine; Liposarcoma; Nude mice; PDOX; Patient-derived orthotopic xenograft
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Year: 2019 PMID: 31200257 DOI: 10.1016/j.biopha.2019.109093
Source DB: PubMed Journal: Biomed Pharmacother ISSN: 0753-3322 Impact factor: 6.529