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Fusion genes in solid tumors: an emerging target for cancer diagnosis and treatment 被引量:3

Fusion genes in solid tumors: an emerging target for cancer diagnosis and treatment
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摘要 Studies over the past decades have uncovered fusion genes, a class of oncogenes that provide immense diagnostic and therapeutic advantages because of their tumor-specific expression. Originally associated with hemotologic cancers, fusion genes have recently been discovered in a wide array of solid tumors, including sarcomas, carcinomas, and tumors of the central nervous system. Fusion genes are attractive as both therapeutic targets and diagnostic tools due to their inherent expression in tumor tissue alone. Therefore, the discovery and elucidation of fusion genes in various cancer types may provide more effective therapies in the future for cancer patients. Studies over the past decades have uncovered fusion genes, a class of oncogenes that provide immense diagnostic and therapeutic advantages because of their tumor-specific expression. Originally associated with hemotologic cancers, fusion genes have recently been discovered in a wide array of solid tumors, including sarcomas, carcinomas, and tumors of the central nervous system. Fusion genes are attractive as both therapeutic targets and diagnostic tools due to their inherent expression in tumor tissue alone. Therefore, the discovery and elucidation of fusion genes in various cancer types may provide more effective therapies in the future for cancer patients.
出处 《Chinese Journal of Cancer》 SCIE CAS CSCD 2013年第11期594-603,共10页
基金 supported in part by the grant from the National Institutes of Health through MD Anderson Cancer Center (No. CA016672)
关键词 融合基因 癌症患者 治疗性 实体瘤 肿瘤组织 中枢神经系统 诊断工具 特异性表达 Cancer genomics, fusion genes, tumorigenesis, therapy, chromosomal instability
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  • 1Gilbert W, Maxam A. The nucleotide sequence of the lac operator. Proc Natl Acad Sci USA, 1973,70:3581-3584. 被引量:1
  • 2Sanger F, Nicklen S, Coulson AR. DNA sequencing with chainterminating inhibitors. Proc Natl Acad Sci USA, 1977,74:5463- 5467. 被引量:1
  • 3Saiki RK, Scharf S, Faloona F, et al. Enzymatic amplification of beta-globin genomic sequences and restriction site analysis for diagnosis of sickle cell anemia. Science, 1985,230: 1350-1354. 被引量:1
  • 4Schuster SC. Next-generation sequencing transforms today's biology. Nat Methods, 2008,5:16-18. 被引量:1
  • 5Rowley JD. Letter: a new consistent chromosomal abnormality in chronic myelogenous leukaemia identified by quinacrine fluorescence and Giemsa staining. Nature, 1973,243:290-293. 被引量:1
  • 6Lifshitz B, Fainstein E, Marcelle C, et al. bcr genes and transcripts. Oncogene, 1988,2:113-117. 被引量:1
  • 7Nowell PC, Hungerford DA. A minute chromosome in human chronic granulocytic leukemia. Science, 1960,132:1497. 被引量:1
  • 8Dreazen 0, Klisak I, Jones G, et al. Multiple molecular abnormalities in Ph1 chromosome positive acute lymphoblastic-leukemia. Brit J Haematol, 1987,67:319-374. 被引量:1
  • 9Shtivelman E, Lifshitz B, Gale RP, et al. Fused transcript of abl and bcr genes in chronic myelogenous leukemia. Nature, 1985,315:550-554. 被引量:1
  • 10Manolov G, Manolova Y. Marker band in one chromosome-14 from Burkitt lymphomas. Nature, 1972,237:33-34. 被引量:1

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