BioMed Research International
Volume 2016 (2016), Article ID 5170159, 1 page
http://dx.doi.org/10.1155/2016/5170159

Editorial

Molecular Imaging for Personalized Medicine

James Russell,¹ Jie Tian,² Seigo Kinuya,³ Baozhong Shen,⁴ and Xiao-Feng Li⁵

¹Memorial Sloan Kettering Cancer Center, New York, NY, USA
²Chinese Academy of Sciences, Beijing, China
³Kanazawa University, Kanazawa, Japan
⁴Harbin Medical University, Harbin, China
⁵University of Louisville, Louisville, KY, USA

Received 23 June 2016; Accepted 23 June 2016

Copyright © 2016 James Russell et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

This issue is devoted to molecular imaging in the context of personalized medicine. Recent advances in biology, particularly genomic and expression screens, have made it possible to hope that treatment can be matched very specifically to the patient’s disease, as characterized at the molecular level. In oncology, where hopes for personalized medicine are perhaps highest, tumors will be treated based on the specific mutations that drive their unrestrained growth, rather than on their site of origin. For all branches of medicine, there is also the potential for matching drug dosage to the individual’s drug metabolism profile, established through genetic analysis.

Along with genomic information, molecular imaging will be crucial in the development of personalized medicine. Molecular imaging—essentially any imaging procedure that delivers some information on a disease state, beyond the purely anatomical—is an incredibly diverse area of research, covering every disease state and imaging modality, with astonishing innovation in developing novel imaging agents. However, there are three aims that commonly emerge in the literature: to image some physiological/biological state that will be diagnostic/predictive; to observe treatment response; and to image the accumulation of drug in the lesion, an approach known as theranostics.

Appropriately, all these aims are represented in the six articles featured here. Dr. X. Li et al. (Shenyang, China) report the successful production of a ⁶⁸Ga labeled rhodamine based probe for PET imaging of mitochondrial potential in tumors, with the biology of probe uptake still to be clarified. Dr. W. Zhou et al. (Hohhot, China) demonstrate that N-11C methyl dopamine is a promising PET imaging agent for cardiac reperfusion injury, comparing it with a commonly used PET tracer of perfusion, ¹³N ammonium in a swine model. X. Wang et al., also from Hohhot, present a comparison between labeled Annexin-V and methyl diphosphonate, in the detection of femoral head osteonecrosis in glucocorticoid treated rabbits, which indicates an advantage for Annexin-V in earlier detection of pathologic changes. B.-C. Ahn (Daegu, Republic of Korea) presents a review of theranostic imaging in the context of radioiodine treatment of differentiated thyroid cancer, while G. Liu et al. (Shenyang) make a practical contribution to this disease by demonstrating the superiority of ¹³¹I imaging compared to in identifying remaining tissue in patients who have undergone surgery. Finally, Q. Liu et al. (Shanghai) publish a meta-analysis of ¹⁸F-FDG PET/CT imaging and MRI in determining pathological complete response in breast cancer patients receiving neoadjuvant chemotherapy.

We hope that the reader will find something stimulating in this selection from an exciting and rapidly expanding area of research.

Acknowledgments

As guest editors we would like to thank the featured authors for their high quality contributions.

James Russell
Jie Tian
Seigo Kinuya
Baozhong Shen
Xiao-Feng Li