Malignancies of the lungs, both primary and metastatic, are the leading cause of death worldwide. Over 1.5 million new cases of primary lung cancer are diagnosed annually worldwide with a dismal 5-year survival rate of approximately 15 %, which remains unchanged despite major efforts and medical advances. As expected, survival for patients with lung metastases is even worse at about 5 %. Early detection and staging are fundamental in improving survival rates and selecting the most effective treatment strategies. Recently, nanoparticles have been developed for imaging and treating various cancers, including pulmonary malignancies. In this work, three different examples of nanoparticle configurations for cancer theranosis are presented, namely conventional spherical polymeric nanoparticles with a diameter of ~150 nm; and discoidal mesoporous silicon nanoconstructs and discoidal polymeric nanoconstructs with a diameter of ~1,000 nm and a height of 400 and 500 nm, respectively. The spherical nanoparticles accumulate in tumors by means of the well-known enhanced permeation and retention effect, whereas sub-micrometer discoidal nanoconstructs are rationally designed to adhere firmly to the tortuous tumor vasculature. All three nanoparticles are characterized for their in vivo performance in terms of magnetic resonance, positron-emission tomography (PET), and optical imaging. Preliminary data on the in vivo and ex vivo PET/CT imaging of breast cancer metastasis in the lungs using discoidal nanoconstructs is presented. In conclusion, opportunities for nanoparticle-based theranosis in primary lung cancer and pulmonary metastasis are presented and discussed.
|Number of pages||11|
|Journal||Clinical and Translational Imaging|
|Publication status||Published - 2014 Oct 25|
Bibliographical noteFunding Information:
Acknowledgments The authors would like to thank Dr. Henry Dirk Sostman for useful discussion. This work was partially supported by the Cancer Prevention Research Institute of Texas through the Grant CPRIT RP110262; the US National Cancer Institute (USA) (NIH) U54CA143837 and U54CA151668, and the European Research Council under the European Union’s Seventh Framework Programme (FP7/2007-2013)/ERC Grant agreement no 616695. M. Ferrari acknowledges the Ernest Cockrell Jr Distinguished Endowed Chair. The authors would like to thank M. Landry for assistance with the graphical work.
© 2014, Italian Association of Nuclear Medicine and Molecular Imaging.
All Science Journal Classification (ASJC) codes
- Radiology Nuclear Medicine and imaging