Abstract
We investigated the use of cucurbitacin B, a plant-derived tetracyclic triterpenoid, as a single agent or in combination with methotrexate (MTX) for human osteosarcoma (OS) treatment. Cucurbitacin B showed antiproliferative activity against seven human OS cell lines in vitro accompanying G2/M cell cycle arrest, apoptosis, and inhibition of ERK, Akt, and mTOR proteins. Cucurbitacin B in combination with MTX synergistically inhibited OS cell growth in vitro. Low-dose cucurbitacin B (LD-CuB, 0.5 mg/kg body weight) or low-dose MTX (LD-MTX, 150 mg/kg) failed to decrease the size of human OS xenografts in nude mice. However, combined therapy at identical concentrations inhibited tumor growth by 62% vs. LD-CuB and 81% vs. LD-MTX (p<0.001). Strikingly, the effect persisted even when the dose of MTX was decreased by two thirds (VLD-MTX, 50 mg/kg). In conclusion, cucurbitacin B alone or in combination with MTX shows promising antiproliferative activity against human OS.
Copyright © 2011 Elsevier Ireland Ltd. All rights reserved.
Publication types
-
Research Support, N.I.H., Extramural
-
Research Support, Non-U.S. Gov't
MeSH terms
-
Animals
-
Antimetabolites, Antineoplastic / therapeutic use*
-
Apoptosis / drug effects
-
Blotting, Western
-
Bone Neoplasms / drug therapy*
-
Bone Neoplasms / metabolism
-
Bone Neoplasms / pathology
-
Cell Cycle / drug effects
-
Cell Proliferation / drug effects
-
Dose-Response Relationship, Drug
-
Drug Synergism
-
Female
-
Humans
-
Immunoenzyme Techniques
-
Methotrexate / therapeutic use*
-
Mice
-
Mice, Nude
-
Mitogen-Activated Protein Kinases / metabolism
-
Osteosarcoma / drug therapy*
-
Osteosarcoma / metabolism
-
Osteosarcoma / pathology
-
Phosphatidylinositol 3-Kinase / metabolism
-
Phosphorylation / drug effects
-
Proto-Oncogene Proteins c-akt / metabolism
-
TOR Serine-Threonine Kinases / metabolism
-
Triterpenes / therapeutic use*
-
Tumor Cells, Cultured
-
Xenograft Model Antitumor Assays
Substances
-
Antimetabolites, Antineoplastic
-
Triterpenes
-
cucurbitacin B
-
Phosphatidylinositol 3-Kinase
-
Proto-Oncogene Proteins c-akt
-
TOR Serine-Threonine Kinases
-
Mitogen-Activated Protein Kinases
-
Methotrexate