SAIC-Frederick, National Cancer Institute at Frederick, Frederick, MD 21702, USA.
Nat Rev Clin Oncol. 2010 May;7(5):251-65. doi: 10.1038/nrclinonc.2010.41. Epub 2010 Mar 30.
Rapid technical advances in DNA sequencing and genome-wide association studies are driving the discovery of the germline and somatic mutations that are present in different cancers. Mutations in genes involved in cellular signaling are common, and often shared by tumors that arise in distinct anatomical locations. Here we review the most important molecular changes in different cancers from the perspective of what should be analyzed on a routine basis in the clinic. The paradigms are EGFR mutations in adenocarcinoma of the lung that can be treated with gefitinib, KRAS mutations in colon cancer with respect to treatment with EGFR antibodies, and the use of gene-expression analysis for ER-positive, node-negative breast cancer patients with respect to chemotherapy options. Several other examples in both solid and hematological cancers are also provided. We focus on how disease subtypes can influence therapy and discuss the implications of the impending molecular diagnostic revolution from the point of view of the patients, clinicians, and the diagnostic and pharmaceutical companies. This paradigm shift is occurring first in cancer patient management and is likely to promote the application of these technologies to other diseases.
DNA 测序和全基因组关联研究的快速技术进步正在推动对不同癌症中存在的种系和体细胞突变的发现。参与细胞信号转导的基因的突变很常见,而且经常存在于不同解剖部位发生的肿瘤中。在这里,我们从临床上应常规分析的角度,综述不同癌症中最重要的分子变化。范例包括:针对肺腺癌的 EGFR 突变,可使用吉非替尼治疗;针对结肠癌的 KRAS 突变,可使用 EGFR 抗体治疗;以及针对 ER 阳性、淋巴结阴性的乳腺癌患者的化疗选择,可使用基因表达分析。还提供了其他一些实体瘤和血液系统癌症的例子。我们重点关注疾病亚型如何影响治疗,并从患者、临床医生和诊断及制药公司的角度讨论即将到来的分子诊断革命的影响。这种模式转变首先出现在癌症患者管理中,并且可能会促使这些技术应用于其他疾病。