Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
5
pubmed:dateCreated
2006-6-12
pubmed:abstractText
Chondrosarcoma is a difficult musculoskeletal tumor to treat. Surgical treatment leads to severe disability, with high rates of local recurrence and life threat. No adjuvant therapy is effective in differentiated chondrosarcomas. Bisphosphonates (BPs) are a class of molecules which is effective in malignant bone diseases. The aim of the present study was to determine the effects of zoledronic acid (ZOL) on chondrosarcoma tumor progression. ZOL was tested in vivo (s.c. 100 microg/kg, twice a week) in a rat chondrosarcoma model and in vitro (10(-7)-10(-4) M) on cells derived from this model. Two types of animal models were assessed, the first simulated development after intralesional curettage, the second nonoperative development of the tumor. Cell proliferation, caspase-1, -3 activities and cell cycle analysis were studied. The results revealed that ZOL slows down primary tumor development, tumor progression after intralesional curretage and increases overall survival. ZOL inhibits cell proliferation and increases cell death, with no significant variation of caspase-1 and -3 activities and cell cycle profiles. The present study demonstrates for the first time that in addition to surgery, the therapy of chondrosarcoma with BPs might be beneficial. Because of these first results, new therapeutic approaches of chondrosarcoma must be considered, mainly for low grade chondrosarcoma when disabling operation is planned and when only intralesional resection can be undertaken.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Sep
pubmed:issn
0020-7136
pubmed:author
pubmed:copyrightInfo
Copyright 2006 Wiley-Liss, Inc.
pubmed:issnType
Print
pubmed:day
1
pubmed:volume
119
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
980-4
pubmed:dateRevised
2007-7-24
pubmed:meshHeading
pubmed-meshheading:16570273-Animals, pubmed-meshheading:16570273-Antineoplastic Agents, pubmed-meshheading:16570273-Apoptosis, pubmed-meshheading:16570273-Bone Density Conservation Agents, pubmed-meshheading:16570273-Caspase 1, pubmed-meshheading:16570273-Caspase 3, pubmed-meshheading:16570273-Caspases, pubmed-meshheading:16570273-Cell Cycle, pubmed-meshheading:16570273-Cell Proliferation, pubmed-meshheading:16570273-Chemotherapy, Adjuvant, pubmed-meshheading:16570273-Chondrosarcoma, pubmed-meshheading:16570273-Curettage, pubmed-meshheading:16570273-Diphosphonates, pubmed-meshheading:16570273-Disease Progression, pubmed-meshheading:16570273-Imidazoles, pubmed-meshheading:16570273-Male, pubmed-meshheading:16570273-Neoplasm Recurrence, Local, pubmed-meshheading:16570273-Rats, pubmed-meshheading:16570273-Rats, Sprague-Dawley, pubmed-meshheading:16570273-Survival Analysis
pubmed:year
2006
pubmed:articleTitle
Zoledronic acid slows down rat primary chondrosarcoma development, recurrent tumor progression after intralesional curretage and increases overall survival.
pubmed:affiliation
INSERM, ERI 7, Nantes, France. fgouin@chu-nantes.fr
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't