Pharmacogenetics of the Primary and Metastatic Osteosarcoma: Gene Expression Profile Associated with Outcome

被引:4
|
作者
Trujillo-Paolillo, Alini [1 ,2 ]
Tesser-Gamba, Francine [1 ]
Alves, Maria Teresa Seixas [3 ]
Garcia Filho, Reynaldo Jesus [4 ]
Oliveira, Renato [5 ]
Petrilli, Antonio Sergio [6 ]
Toledo, Silvia Regina Caminada [1 ,2 ]
机构
[1] Univ Fed Sao Paulo, Pediat Oncol Inst IOP GRAACC, Genet Lab, Rua Botucatu, BR-04023062 Sao Paulo, SP, Brazil
[2] Univ Fed Sao Paulo, Dept Clin & Expt Oncol, Rua Dr Diogo Faria, BR-04037003 Sao Paulo, SP, Brazil
[3] Univ Fed Sao Paulo, Dept Pathol, Rua Botucatu, BR-04023062 Sao Paulo, SP, Brazil
[4] Univ Fed Sao Paulo, Dept Orthoped Surg & Traumatol, Rua Borges Lagoa, BR-04038031 Sao Paulo, SP, Brazil
[5] Univ Fed Sao Paulo, Dept Thorac Surg, Rua Napoleao Barros, BR-04024002 Vila Clementino, SP, Brazil
[6] Univ Fed Sao Paulo, Pediat Oncol Inst IOP GRAACC, Dept Pediat, Rua Botucatu, BR-04023062 Sao Paulo, SP, Brazil
基金
瑞典研究理事会; 巴西圣保罗研究基金会;
关键词
osteosarcoma; metastatic osteosarcoma; pharmacogenetics; gene expression; prognostic markers; treatment response; HIGH-GRADE; CANCER; POLYMORPHISMS; RESISTANCE; DRUGS;
D O I
10.3390/ijms24065607
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Osteosarcoma (OS) is the most common malignant bone tumor in children and adolescents. In recent decades, OS treatment has reached a plateau and drug resistance is still a major challenge. Therefore, the present study aimed to analyze the expression of the genes related to pharmacogenetics in OS. The expression of 32 target genes in 80 paired specimens (pre-chemotherapeutic primary tumor, post-chemotherapeutic primary tumor and pulmonary metastasis) obtained from 33 patients diagnosed with OS were analyzed by the real-time PCR methodology. As the calibrators (control), five normal bone specimens were used. The present study identified associations between the OS outcome and the expression of the genes TOP2A, DHFR, MTHFR, BCL2L1, CASP3, FASLG, GSTM3, SOD1, ABCC1, ABCC2, ABCC3, ABCC5, ABCC6, ABCC10, ABCC11, ABCG2, RALBP1, SLC19A1, SLC22A1, ERCC1 and MSH2. In addition, the expression of the ABCC10, GGH, GSTM3 and SLC22A1 genes were associated with the disease event, and the metastasis specimens showed a high expression profile of ABCC1, ABCC3 and ABCC4 genes and a low expression of SLC22A1 and ABCC10 genes, which is possibly an important factor for resistance in OS metastasis. Therefore, our findings may, in the future, contribute to clinical management as prognostic factors as well as possible therapeutic targets.
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页数:14
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