4.3 Review

SPECT and PET radiopharmaceuticals for molecular imaging of apoptosis: from bench to clinic

期刊

ONCOTARGET
卷 8, 期 12, 页码 20476-20495

出版社

IMPACT JOURNALS LLC
DOI: 10.18632/oncotarget.14730

关键词

SPECT; PET; radiopharmaceuticals; apoptosis; clinical status

资金

  1. National Natural Science Foundation of China [81671756, 81271634, 81601554]
  2. National Key Clinical Specialist Construction Programs of China [2013-544]

向作者/读者索取更多资源

Owing to the central role of apoptosis in many human diseases and the widespread application of apoptosis-based therapeutics, molecular imaging of apoptosis in clinical practice is of great interest for clinicians, and holds great promises. Based on the well-defined biochemical changes for apoptosis, a rich assortment of probes and approaches have been developed for molecular imaging of apoptosis with various imaging modalities. Among these imaging techniques, nuclear imaging (including single photon emission computed tomography and positron emission tomography) remains the premier clinical method owing to their high specificity and sensitivity. Therefore, the corresponding radiopharmaceuticals have been a major focus, and some of them like 99mTc-Annexin V, 18F-ML-10, 18F-CP18, and 18F-ICMT-11 are currently under clinical investigations in Phase I/II or Phase II/III clinical trials on a wide scope of diseases. In this review, we summarize these radiopharmaceuticals that have been widely used in clinical trials and elaborate them in terms of radiosynthesis, pharmacokinetics and dosimetry, and their applications in different clinical stages. We also explore the unique features required to qualify a desirable radiopharmaceutical for imaging apoptosis in clinical practice. Particularly, a perspective of the impact of these clinical efforts, namely, apoptosis imaging as predictive and prognostic markers, early-response indicators and surrogate endpoints, is also the highlight of this review.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.3
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据