期刊文献+

横纹肌肉瘤的分子生物学研究进展 被引量:5

Research Progress in Molecular Biology of Rhabdomyosarcoma
下载PDF
导出
摘要 横纹肌肉瘤是儿童最常见恶性软组织肉瘤,其可能来源于分化异常的骨骼肌。横纹肌肉瘤具有高度的非整倍体水平,其发生发展与PAX—FOX01基因融合、癌基因、抑癌基因、多药耐药基因等密切相关。分子生物学方面的研究有助于临床诊断及治疗。本文综述了近年来横纹肌肉瘤分子生物学的研究进展。 Rhabdomyosareoma,the most common pediatric soft tissue sareoma, eomes from deregulation of the skeletal myogenesis. Rhabdomyosareoma is in a high degree of aneuploidy. The initiation and development of rhabdomyosarcoma are correlated with PAX-FOXO1 fusion gene,oneogene, anti-oncogene and muhidrug resistanee gene. Researches of rhabdomyosareoma are helpful to diagnosis and treatment. This article reviewed the molecular biology of rhabdomyosareoma.
出处 《医学综述》 2009年第4期514-517,共4页 Medical Recapitulate
基金 国家自然科学基金面上项目(30672359)
关键词 横纹肌肉瘤 融合基因 非整倍体 癌基因 Rhabdomyosarcoma Fusion gene Aneuploid Oncogene
  • 相关文献

参考文献25

  • 1高志安,张世羽,杨光华.横纹肌肉瘤的临床病理分析[J].锦州医学院学报,2000,21(2):1-4. 被引量:2
  • 2Goldstein M, Meller I, Issakov J, et al. Novel genes implicated in embryonal, alveolar, and pleomorphic rhabdomyosarcoma: a cytogenetic and molecular analysis of primary tumors [ J 1. Neoplasia, 2006,8 (5) :332-343.
  • 3Schaaf GJ, Ruijter JM, van Ruissen F, et al. Full transcnptome analysis of rhabdomyosarcoma, normal, and fetal skeletal muscle: statistical comparison of multiple SAGE libraries [ J ]. FASEB J, 2005,19(3) :404-406.
  • 4Hanks S, Coleman K, Summersgill B,et al. Comparative genomic hybridization and BUB1 B mutation analyses in childhood cancers associated with mosaic variegated aneuploidy syndrome [ J ]. Cancer Left,2006,239 (2) :234-238.
  • 5Duesberg P, Fabarius A, Hehlmann R. Aneuploidy, the primary cause of the multilateral gcnomic instability of neoplastic and preneoplastic cells[J]. IUBMB Life,2004,56(2) :65-81.
  • 6Ragazzini P,Gamberi G,Pazzaglia L,et al. Amplification of CDK4, MDM2, SAS and GLI genes in leiomyosarcoma, alveolar and embry- onal rhabdomyosarcoma [ J ]. Histol Histopathol, 2004, 19 ( 2 ) : 401-411.
  • 7Kilpatrick SE, Teot LA, Geisinger KR, et al. Relationship of DNA ploidy to histology and prognosis in rhabdomyosarcoma. Comparison of flow cytometry and image analysis [ J ]. Cancer, 1994,74 (12): 3227-3233.
  • 8Kratz CP, Steinemann D, Niemeyer CM, et al. Uniparental disomy at chromosome 11 p15.5 followed by HRAS mutations in embryonal rhabdomyosarcoma :lessons from Costello syndrome [ J ]. Hum Mol Genet, 2007,16 ( g ) : 374-379.
  • 9Bridge JA, Liu J, Weiboh V, et al. Novel genomic imbalances in embryonal rhabdomyosarcoma revealed by comparative genomic hy- bridization and fluorescence in situ hybridization: an intergroup rhabdomyosarcoma study [ J ]. Genes Chromosomes Cancer, 2000, 27(4) :337-344.
  • 10Ho RH,Johnson J,Dev VG,et al. A novel t(2;20) (q35;p12) in embryonal rhabdomyosarcoma[ J]. Cancer Genet Cytogenet,2004, 151 ( 1 ) :73-77.

共引文献1

同被引文献57

引证文献5

二级引证文献17

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部