The combination of gemcitabine and docetaxel arrests a doxorubicin-resistant dedifferentiated liposarcoma in a patient-derived orthotopic xenograft model

Biomed Pharmacother. 2019 Sep:117:109093. doi: 10.1016/j.biopha.2019.109093. Epub 2019 Jun 11.

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.

Keywords: Docetaxel; Gemcitabine; Liposarcoma; Nude mice; PDOX; Patient-derived orthotopic xenograft.

MeSH terms

  • Animals
  • Antineoplastic Combined Chemotherapy Protocols / pharmacology*
  • Deoxycytidine / analogs & derivatives*
  • Deoxycytidine / pharmacology
  • Disease Models, Animal
  • Docetaxel / pharmacology*
  • Doxorubicin / pharmacology*
  • Drug Resistance, Neoplasm / drug effects*
  • Gemcitabine
  • Heterografts / drug effects
  • Humans
  • Indazoles
  • Liposarcoma / drug therapy*
  • Male
  • Mice
  • Mice, Nude
  • Neoplasm Recurrence, Local / drug therapy
  • Pyrimidines / pharmacology
  • Sulfonamides / pharmacology
  • Tumor Burden / drug effects
  • Xenograft Model Antitumor Assays / methods

Substances

  • Indazoles
  • Pyrimidines
  • Sulfonamides
  • Deoxycytidine
  • Docetaxel
  • pazopanib
  • Doxorubicin
  • Gemcitabine