Walters Denise Katherine, Steinmann Patrick, Langsam Bettina, Schmutz Silvia, Born Walter, Fuchs Bruno
Laboratory for Orthopaedic Research, Department of Orthopaedics, Balgrist University Hospital, University of Zurich, Zurich, Switzerland.
Anticancer Res. 2008 Mar-Apr;28(2A):673-9.
Osteosarcoma (OS) is an aggressive bone malignancy that primarily affects children and adolescents. Patients with metastatic disease at diagnosis have only a 20% survival rate. The poor survival rate of these patients is largely due to their lack of responsiveness to chemotherapy. However, the mechanisms underlying osteosarcoma chemoresistance remain unknown.
The effect of cisplatin, doxorubicin and etoposide was examined on OS cell lines. Affymetric Genechip analysis was used to examine differential gene expression.
A correlation between increasing metastatic potential and increasing chemoresistance was observed in the MG-63 cell line and sub-line model. Microarray analysis of these cell lines revealed the differential expression of several genes potentially involved in chemoresistance including ABCG2, ADD3, NMT2, WNTSa and PTN.
The identification of genes contributing to chemoresistance and determining the role these genes play is critical in characterizing patient responsiveness and overcoming chemoresistance in osteosarcoma patients.
骨肉瘤(OS)是一种侵袭性骨恶性肿瘤,主要影响儿童和青少年。诊断时患有转移性疾病的患者生存率仅为20%。这些患者生存率低主要是因为他们对化疗缺乏反应。然而,骨肉瘤化疗耐药的潜在机制仍不清楚。
检测顺铂、阿霉素和依托泊苷对骨肉瘤细胞系的作用。采用基因芯片分析检测基因表达差异。
在MG-63细胞系和亚系模型中观察到转移潜能增加与化疗耐药性增加之间的相关性。对这些细胞系的微阵列分析揭示了几个可能参与化疗耐药的基因的差异表达,包括ABCG2、ADD3、NMT2、WNTSa和PTN。
鉴定导致化疗耐药的基因并确定这些基因所起的作用对于表征患者反应性和克服骨肉瘤患者的化疗耐药性至关重要。