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CANINE ONCOGENOMICS: WHAT IS IN OUR GENES?

机译:犬oncocogomics:什么是我们的基因?

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Cancer can be defined as a genetic disease. Many different mutations lead to the development of a tumor and others to its subsequent metastatic spread, these include the activation of oncogenes and inactivation of tumor suppressor genes. The multi-step pathogenesis of cancer has been described by many, although most notably by Hanahan and Weinberg. These include manipulation of growth factors, loss of growth inhibition, evading programmed cell death, inhibition of cellular senescence/aging and the ability to metastasize. Mutations described in canine cancers are a more recent development, with non-candidate approaches made possible by the publishing of the canine genome in 2005. A variety of high throughput methods are now available for interrogating canine cancers including RT-PCR, PARR, oligonucleotide and SNP microarrays and comparative genomic hybridization (CGH) technologies. Applications of each technology will be briefly explored in the following review. Lastly, the clinical utility of genediscovery will be emphasized with descriptions of canine clinical trials utilizing novel targeted therapies.
机译:癌症可以定义为遗传疾病。许多不同的突变导致肿瘤和其他肿瘤的发展到其随后的转移扩散,其中包括肿瘤抑制基因的癌培素和失活的激活。许多人已经描述了癌症的多步调发病机制,尽管由Hanahan和Weinberg最有意义地说明。这些包括操纵生长因子,生长抑制丧失,逃避编程的细胞死亡,抑制细胞衰老/老化以及转移的能力。犬癌中描述的突变是最近的发展,通过2005年犬类基因组出版的非候选方法。现在可以用于询问犬癌,包括RT-PCR,Parr,寡核苷酸和寡核苷酸和SNP微阵列和对比基因组杂交(CGH)技术。在以下审查中,将在以下审查中简要探讨各种技术的应用。最后,利用新型靶向疗法的犬临床试验说明了Genediscovery的临床效用。

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