Publication date: October 2016
Source:Biomaterials, Volume 104
Author(s): Rajesh Kumar, Eun-Joong Kim, Jiyou Han, Hyunseung Lee, Weon Sup Shin, Hyun Min Kim, Sankarprasad Bhuniya, Jong Seung Kim, Kwan Soo Hong
Hypoxia, a distinguished feature of various solid tumors, has been considered as a key marker for tumor progression. Inadequate vasculature and high interstitial pressures result in relatively poor drug delivery to these tumors. Herein, we developed an antitumor theranostic agent, 4, which is activated in hypoxic conditions and can be used for the diagnosis and treatment of solid tumors. Compound 4, bearing biotin, a tumor-targeting unit, and SN38, an anticancer drug, proved to be an effective theranostic agent for solid tumors. SN38 plays a dual role: as an anticancer drug for therapy and as a fluorophore for diagnosis, thus avoids an extra fluorophore and limits cytotoxicity. Compound 4, activated in the hypoxic environment, showed high therapeutic activity in A549 and HeLa cells and spheroids. In vivo imaging of solid tumors confirmed the tumor-specific localization, deep tissue penetration and activation of compound 4, as well as the production of a strong anticancer effect through the inhibition of tumor growth in a xenograft mouse model validating it as a promising strategy for the treatment of solid tumors.
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Σφακιανάκης Αλέξανδρος
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- Case 22-2016: A 65-Year-Old Man with Syncope, Dysp...
- Randomized trial comparing efficacies of zoledrona...
- Nerve growth factor: role in growth, differentiati...
- Safety of interferon-free therapies for chronic he...
- Natural Convection Coupled with Thermal Radiation ...
- Effects of oral carbohydrate with amino acid solut...
- Machine learning based methodology to identify cel...
- Superhydrophobic materials for biomedical applicat...
- In-situ second harmonic generation by cancer cell ...
- Hypoxia-directed and activated theranostic agent: ...
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- Occurrence of hepatotoxicity with pazopanib and ot...
- A multi-centred randomised trial of radical surger...
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