Translational Research of Optical Molecular Imaging for Personalized Medicine

被引:4
作者
Qin, C. [1 ,2 ]
Ma, X. [1 ]
Tian, J. [1 ,3 ]
机构
[1] Chinese Acad Sci, Inst Automat, Key Lab Mol Imaging, Beijing 100190, Peoples R China
[2] Chinese Acad Sci, Bur Acad Local Cooperat, Beijing 100864, Peoples R China
[3] Xidian Univ, Sch Life Sci & Technol, Xian 710071, Shaanxi, Peoples R China
基金
北京市自然科学基金; 中国国家自然科学基金;
关键词
Drug development; molecular imaging; multi-modality fusion; optical imaging; personalized medicine; translational research; PROTEIN-PROTEIN INTERACTIONS; CERENKOV LUMINESCENCE TOMOGRAPHY; BIOLUMINESCENCE TOMOGRAPHY; RENILLA-LUCIFERASE; LIGHT TRANSPORT; FINITE-ELEMENT; BREAST-CANCER; MOUSE; RECONSTRUCTION; EXPRESSION;
D O I
10.2174/1566524013666131111123201
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
In the medical imaging field, molecular imaging is a rapidly developing discipline and forms many imaging modalities, providing us effective tools to visualize, characterize, and measure molecular and cellular mechanisms in complex biological processes of living organisms, which can deepen our understanding of biology and accelerate preclinical research including cancer study and medicine discovery. Among many molecular imaging modalities, although the penetration depth of optical imaging and the approved optical probes used for clinics are limited, it has evolved considerably and has seen spectacular advances in basic biomedical research and new drug development. With the completion of human genome sequencing and the emergence of personalized medicine, the specific drug should be matched to not only the right disease but also to the right person, and optical molecular imaging should serve as a strong adjunct to develop personalized medicine by finding the optimal drug based on an individual's proteome and genome. In this process, the computational methodology and imaging system as well as the biomedical application regarding optical molecular imaging will play a crucial role. This review will focus on recent typical translational studies of optical molecular imaging for personalized medicine followed by a concise introduction. Finally, the current challenges and the future development of optical molecular imaging are given according to the understanding of the authors, and the review is then concluded.
引用
收藏
页码:1579 / 1590
页数:12
相关论文
共 90 条
[1]  
Allen JE, 2009, CANCER BIOL THER, V8, P101
[2]   Optical tomography: forward and inverse problems [J].
Arridge, Simon R. ;
Schotland, John C. .
INVERSE PROBLEMS, 2009, 25 (12)
[3]   Optical tomography in medical imaging [J].
Arridge, SR .
INVERSE PROBLEMS, 1999, 15 (02) :R41-R93
[4]   Review of biomedical optical imaging-a powerful, non-invasive, non-ionizing technology for improving in vivo diagnosis [J].
Balas, Costas .
MEASUREMENT SCIENCE AND TECHNOLOGY, 2009, 20 (10)
[5]   Comparison of light transport models based on finite element and the discrete ordinates methods in view of optical tomography applications [J].
Balima, O. ;
Charette, A. ;
Marceau, D. .
JOURNAL OF COMPUTATIONAL AND APPLIED MATHEMATICS, 2010, 234 (07) :2259-2271
[6]   An Efficient Numerical Method for General Lp Regularization in Fluorescence Molecular Tomography [J].
Baritaux, Jean-Charles ;
Hassler, Kai ;
Unser, Michael .
IEEE TRANSACTIONS ON MEDICAL IMAGING, 2010, 29 (04) :1075-1087
[7]   Optical imaging of Renilla luciferase reporter gene expression in living mice [J].
Bhaumik, S ;
Gambhir, SS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (01) :377-382
[8]   Hyperspectral and multispectral bioluminescence optical tomography for small animal imaging [J].
Chaudhari, AJ ;
Darvas, F ;
Bading, JR ;
Moats, RA ;
Conti, PS ;
Smith, DJ ;
Cherry, SR ;
Leahy, RM .
PHYSICS IN MEDICINE AND BIOLOGY, 2005, 50 (23) :5421-5441
[9]   A Cy5.5-labeled phage-displayed peptide probe for near-infrared fluorescence imaging of tumor vasculature in living mice [J].
Chen, Kai ;
Yap, Li-Peng ;
Park, Ryan ;
Hui, Xiaoli ;
Wu, Kaichun ;
Fan, Daiming ;
Chen, Xiaoyuan ;
Conti, Peter S. .
AMINO ACIDS, 2012, 42 (04) :1329-1337
[10]  
Cherry SR, 2004, PHYS MED BIOL, V49, pR13, DOI 10.1088/0031-9155/49/3/R01