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Pamidronate, farnesyl transferase, and geranylgeranyl transferase‐I inhibitors affects cell proliferation, apoptosis, and OPG/RANKL mRNA expression in stromal cells of giant cell tumor of bone
Author(s) -
Lau Carol P.Y.,
Huang Lin,
Tsui Stephen K.W.,
Ng Patrick K.S.,
Leung PuiYin.,
Kumta Shekhar M.
Publication year - 2011
Publication title -
journal of orthopaedic research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.041
H-Index - 155
eISSN - 1554-527X
pISSN - 0736-0266
DOI - 10.1002/jor.21249
Subject(s) - stromal cell , viability assay , rankl , apoptosis , cancer research , combination therapy , chemistry , cell cycle , cell growth , pharmacology , biology , biochemistry , activator (genetics) , receptor
Giant cell tumor (GCT) is the most common nonmalignant primary bone tumor reported in Hong Kong. It usually affects young adults between the ages of 20 and 40. This tumor is well known for its potential to recur following treatment. To date no effective adjuvant therapy exists for GCT. Our project aimed to study the effects of pamidronate (PAM), farnesyl transferase inhibitor (FTI‐277), geranylgeranyl transferase inhibitor (GGTI‐298), and their combinations on GCT stromal cells (SC). Individual treatment with PAM, FTI‐277, and GGTI‐298, inhibited the cell viability and proliferation of GCT SC in a dose‐dependent way. Combination of FTI‐277 with GGTI‐298 caused synergistic effects in reducing cell viability, and its combination index was 0.49, indicating a strong synergism. Moreover, the combination of FTI‐277 with GGTI‐298 synergistically enhanced cell apoptosis and activated caspase‐3/7, ‐8, and ‐9 activities. PAM induced cell‐cycle arrest at the S‐phase. The combination of PAM with GGTI‐298 significantly increased OPG/RANKL mRNA ratio and activated caspase‐3/7 activity. Our findings support that the combination of bisphosphonates with GGTIs or FTIs with GGTIs may be used as potential adjuvants in the treatment of GCT of bone. © 2010 Orthopaedic Research Society. Published by Wiley Periodicals, Inc. J Orthop Res 29:403–413, 2011