Fushiki Hiroshi, Murakami Yoshihiro, Miyoshi Sosuke, Nishimura Shintaro
Bioimaging Research Laboratories, Astellas Pharma Inc., 21 Miyukigaoka, Tsukuba, Ibaraki, 305-8585, Japan,
Methods Mol Biol. 2015;1219:199-206. doi: 10.1007/978-1-4939-1661-0_15.
Receptor tyrosine kinases play a critical role in cell growth, survival, and proliferation, and are considered potential molecular targets for the treatment of cancer. Although several tyrosine kinase inhibitors (TKIs), such as erlotinib and gefitinib, have demonstrated clinical efficacy via the inhibition of the epidermal growth factor receptor (EGFR), most TKIs are only effective in a small proportion of patients. Positron emission tomography (PET) imaging is a methodology of molecular imaging based on nuclear imaging. PET imaging in combination with radiolabeled TKIs improves accuracy of quantitative imaging strategies and the probability of successful drug development, and may facilitate the stratification of patients. Here, we describe a protocol for PET imaging using radiolabeled TKI in preclinical trials.
受体酪氨酸激酶在细胞生长、存活和增殖中起关键作用,被认为是癌症治疗的潜在分子靶点。尽管几种酪氨酸激酶抑制剂(TKIs),如厄洛替尼和吉非替尼,已通过抑制表皮生长因子受体(EGFR)显示出临床疗效,但大多数TKIs仅对一小部分患者有效。正电子发射断层扫描(PET)成像是一种基于核成像的分子成像方法。PET成像与放射性标记的TKIs相结合可提高定量成像策略的准确性和药物研发成功的概率,并可能有助于患者分层。在此,我们描述了一种在临床前试验中使用放射性标记的TKI进行PET成像的方案。