Hamid Oday
Pfizer Global Research and Development, Ann Arbor Laboratory, Ann Arbor, Mich 48105, USA.
J Am Pharm Assoc (2003). 2004 Jan-Feb;44(1):52-8. doi: 10.1331/154434504322713237.
To describe the role of tyrosine kinase (TK) and its subreceptors in the development of cancer and the role of TK inhibitors in cancer treatment.
Published articles identified through MEDLINE using search terms such as tyrosine kinase, erbB1, erbB2, erbB3, erbB4, epidermal growth factor receptors (EGFR), and EGFR inhibitors. Additional sources were identified from bibliographies in the articles and from Web sites and reports from the National Cancer Institute, American Society of Clinical Oncology, and European Organization for Research and Treatment of Cancer.
Progress in identifying the biochemical and molecular causes of cancer has led to discovery of abnormalities that characterize cancer cells and represent targets for development of drug therapies. TK receptors represent one such target when these are present in elevated quantities and/or aberrant forms. Abnormalities in these cell surface receptors have been correlated with development and progression of cancer, poor response to chemotherapeutic agents, and low survival rates. Several subtypes of TK receptors have been identified, and mutations in these have been associated with neoplasms of the breast, lung, colon, ovaries, and other organs. Approved agents, such as trastuzumab (Herceptin-Genentech) work by blocking a subtype of TK receptors that has been associated with breast cancer growth. Gefitinib (Iressa-AstraZeneca) was recently approved for treatment of non-small-cell lung cancer in patients who have failed treatment with traditional chemotherapeutic agents. Other agents such as cetuximab, erlotinib, and canertinib are in advanced stages of clinical trials and may be available for general clinical use in the next few years.
Cancer continues to be a difficult disease to treat, but newly identified cellular targets have resulted in new medications, and these promising agents are giving hope for additional options for patients with various solid tumors.
描述酪氨酸激酶(TK)及其亚受体在癌症发生发展中的作用以及TK抑制剂在癌症治疗中的作用。
通过MEDLINE检索已发表的文章,检索词包括酪氨酸激酶、erbB1、erbB2、erbB3、erbB4、表皮生长因子受体(EGFR)和EGFR抑制剂。其他资料来源为文章中的参考文献以及美国国立癌症研究所、美国临床肿瘤学会和欧洲癌症研究与治疗组织的网站及报告。
在确定癌症的生化和分子病因方面取得的进展,已导致发现了癌细胞特有的异常情况,这些异常情况是药物治疗开发的靶点。当TK受体数量升高和/或形式异常时,它们就代表这样一个靶点。这些细胞表面受体的异常与癌症的发生发展、对化疗药物的不良反应以及低生存率相关。已确定了几种TK受体亚型,这些亚型中的突变与乳腺、肺、结肠、卵巢和其他器官的肿瘤有关。已获批准的药物,如曲妥珠单抗(赫赛汀 - 基因泰克公司),通过阻断与乳腺癌生长相关的一种TK受体亚型发挥作用。吉非替尼(易瑞沙 - 阿斯利康公司)最近被批准用于治疗传统化疗药物治疗失败的非小细胞肺癌患者。其他药物,如西妥昔单抗、厄洛替尼和卡奈替尼正处于临床试验后期,可能在未来几年可供一般临床使用。
癌症仍然是一种难以治疗的疾病,但新确定的细胞靶点已带来了新药物,这些有前景的药物为患有各种实体瘤的患者提供了更多选择的希望。