TY - JOUR
T1 - Optogenetic technologies in translational cancer research
AU - Malogolovkin, Alexander
AU - Egorov, Alexander D.
AU - Karabelsky, Alexander
AU - Ivanov, Roman A.
AU - Verkhusha, Vladislav V.
N1 - Funding Information:
V.V.V. was supported by the grants GM122567 from the US National Institutes of Health and 61-5956 from the Cancer Foundation Finland . A.M. was supported by the Priority 2030 academic leadership program of the Sechenov First Moscow State Medical University . A.D.E., A.K. and R.A.I. were supported by the projects GTH-RND-2011 and GTH-RND-2112 from the Sirius University of Science and Technology . We apologize to researchers whose work we could not quote here due to space limitations and the focus of this article.
Publisher Copyright:
© 2022 Elsevier Inc.
PY - 2022/11
Y1 - 2022/11
N2 - Gene and cell therapies are widely recognized as future cancer therapeutics but poor controllability limits their clinical applications. Optogenetics, the use of light-controlled proteins to precisely spatiotemporally regulate the activity of genes and cells, opens up new possibilities for cancer treatment. Light of specific wavelength can activate the immune response, oncolytic activity and modulate cell signaling in tumor cells non-invasively, in dosed manner, with tissue confined action and without side effects of conventional therapies. Here, we review optogenetic approaches in cancer research, their clinical potential and challenges of incorporating optogenetics in cancer therapy. We critically discuss beneficial combinations of optogenetic technologies with therapeutic nanobodies, T-cell activation and CAR-T cell approaches, genome editors and oncolytic viruses. We consider viral vectors and nanoparticles for delivering optogenetic payloads and activating light to tumors. Finally, we highlight herein the prospects for integrating optogenetics into immunotherapy as a novel, fast, reversible and safe approach to cancer treatment.
AB - Gene and cell therapies are widely recognized as future cancer therapeutics but poor controllability limits their clinical applications. Optogenetics, the use of light-controlled proteins to precisely spatiotemporally regulate the activity of genes and cells, opens up new possibilities for cancer treatment. Light of specific wavelength can activate the immune response, oncolytic activity and modulate cell signaling in tumor cells non-invasively, in dosed manner, with tissue confined action and without side effects of conventional therapies. Here, we review optogenetic approaches in cancer research, their clinical potential and challenges of incorporating optogenetics in cancer therapy. We critically discuss beneficial combinations of optogenetic technologies with therapeutic nanobodies, T-cell activation and CAR-T cell approaches, genome editors and oncolytic viruses. We consider viral vectors and nanoparticles for delivering optogenetic payloads and activating light to tumors. Finally, we highlight herein the prospects for integrating optogenetics into immunotherapy as a novel, fast, reversible and safe approach to cancer treatment.
KW - CAR-T
KW - CRISPR
KW - Immunotherapy
KW - Oncolytics
KW - Optobodies
KW - Tumor
KW - Viral vector
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U2 - 10.1016/j.biotechadv.2022.108005
DO - 10.1016/j.biotechadv.2022.108005
M3 - Review article
C2 - 35690273
AN - SCOPUS:85132335258
SN - 0734-9750
VL - 60
JO - Biotechnology Advances
JF - Biotechnology Advances
M1 - 108005
ER -