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Oncogenomics: The Future Of Cancer Therapy

机译:肿瘤基因组学:癌症治疗的未来

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At present, cancer accounts for 12% of the 56 million deaths occurring annually, making it one of the leading causes for death. The primary obstacle clinicians face today is that they are not adequately equipped to tackle this imminent threat. However, with the recent developments in the field of oncogenomics, our knowledge of exactly where, why and how tumorigenesis occurs has increased manifold. Genomic technologies such as 'comparative genomic hybridization' and cDNA microarrays have helped to improve our understanding of the genetic basis of cancer. Researchers are presently looking towards developing new anticancer drugs based on the discovery of novel molecular targets. The success stories of agents like Trastuzumab and Gleevec?)used in the therapy of HER-2 positive breast cancers and chronic myelegenous leukemia (CML) respectively, give us hope that not too long from now, oncogenomics will no longer remain a mere research modality, but will be used in clinical practice for the effective therapy of cancer. This article reviews some of the more recent developments in the field of cancer genomics and discusses the current status as well as the future trends. Introduction Despite the advances in medical research, cancer is still one of the leading causes for death. Recently, the International Agency for Research on Cancer (IARC), a branch of the World Health Organization (WHO), published the World Cancer Report, which states that in the year 2000 alone, there were 10 million new cases of cancer reported globally. This figure is predicted to rise by a staggering 50% by the year 2020, due to steadily ageing populations, current trends in smoking prevalence, and unhealthy lifestyles. As per the American Cancer Society estimates, in India alone, at any given time, there are 2.5 million cases of cancer. Table 1 shows the global incidence of cancer in the year 2002. The figures are compiled from the American Cancer Society publications (Parkin et al, 2005).
机译:目前,癌症占每年发生的5600万人死亡的12%,使其成为主要的死亡原因之一。今天,临床医生面临的主要障碍是他们没有足够的能力来应对这一迫在眉睫的威胁。然而,随着肿瘤基因组学领域的最新发展,我们对发生肿瘤发生的确切位置,原因和方式的了解增加了。诸如“比较基因组杂交”和cDNA微阵列之类的基因组技术有助于增进我们对癌症遗传基础的了解。目前,研究人员正在基于发现新的分子靶标来开发新的抗癌药。曲妥珠单抗和格列卫?等药物分别用于治疗HER-2阳性乳腺癌和慢性粒细胞性白血病(CML)的成功故事,使我们希望,从现在起不久以后,肿瘤基因组学将不再仅仅是一种研究方法,但将在临床实践中用于有效治疗癌症。本文回顾了癌症基因组学领域的一些最新进展,并讨论了当前状态以及未来趋势。引言尽管医学研究取得了进步,但是癌症仍然是导致死亡的主要原因之一。最近,世界卫生组织(WHO)的一个分支机构国际癌症研究机构(IARC)发表了《世界癌症报告》,该报告指出,仅在2000年,全球就报告了1000万例新癌症病例。由于人口稳定老龄化,当前吸烟流行趋势和不健康的生活方式,预计到2020年,这一数字将以惊人的速度增长50%。据美国癌​​症协会估计,仅在印度,在任何给定时间,就有250万例癌症病例。表1显示了2002年全球癌症的发病率。这些数据是根据美国癌症协会的出版物编制的(Parkin等,2005)。

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