TY - JOUR
T1 - Tumor-targeted Nanobullets
T2 - Anti-EGFR nanobody-liposomes loaded with anti-IGF-1R kinase inhibitor for cancer treatment
AU - Van Der Meel, Roy
AU - Oliveira, Sabrina
AU - Altintas, Isil
AU - Haselberg, Rob
AU - Van Der Veeken, Joris
AU - Roovers, Rob C.
AU - Van Bergen En Henegouwen, Paul M P
AU - Storm, Gert
AU - Hennink, Wim E.
AU - Schiffelers, Raymond M.
AU - Kok, Robbert J.
PY - 2012/4/30
Y1 - 2012/4/30
N2 - The epidermal growth factor receptor (EGFR) is a validated target for anti-cancer therapy and several EGFR inhibitors are used in the clinic. Over the years, an increasing number of studies have reported on the crosstalk between EGFR and other receptors that can contribute to accelerated cancer development or even acquisition of resistance to anti-EGFR therapies. Combined targeting of EGFR and insulin-like growth factor 1 receptor (IGF-1R) is a rational strategy to potentiate anti-cancer treatment and possibly retard resistance development. In the present study, we have pursued this by encapsulating the kinase inhibitor AG538 in anti-EGFR nanobody-liposomes. The thus developed dual-active nanobody-liposomes associated with EGFR-(over)expressing cells in an EGFR-specific manner and blocked both EGFR and IGF-1R activation, due to the presence of the EGFR-blocking nanobody EGa1 and the anti-IGF-1R kinase inhibitor AG538 respectively. AG538-loaded nanobody-liposomes induced a strong inhibition of tumor cell proliferation even upon short-term exposure followed by a drug-free wash-out period. Therefore, AG538-loaded nanobody-liposomes are a promising anti-cancer formulation due to efficient intracellular delivery of AG538 in combination with antagonistic and downregulating properties of the EGa1 nanobody-liposomes.
AB - The epidermal growth factor receptor (EGFR) is a validated target for anti-cancer therapy and several EGFR inhibitors are used in the clinic. Over the years, an increasing number of studies have reported on the crosstalk between EGFR and other receptors that can contribute to accelerated cancer development or even acquisition of resistance to anti-EGFR therapies. Combined targeting of EGFR and insulin-like growth factor 1 receptor (IGF-1R) is a rational strategy to potentiate anti-cancer treatment and possibly retard resistance development. In the present study, we have pursued this by encapsulating the kinase inhibitor AG538 in anti-EGFR nanobody-liposomes. The thus developed dual-active nanobody-liposomes associated with EGFR-(over)expressing cells in an EGFR-specific manner and blocked both EGFR and IGF-1R activation, due to the presence of the EGFR-blocking nanobody EGa1 and the anti-IGF-1R kinase inhibitor AG538 respectively. AG538-loaded nanobody-liposomes induced a strong inhibition of tumor cell proliferation even upon short-term exposure followed by a drug-free wash-out period. Therefore, AG538-loaded nanobody-liposomes are a promising anti-cancer formulation due to efficient intracellular delivery of AG538 in combination with antagonistic and downregulating properties of the EGa1 nanobody-liposomes.
KW - Combination therapy
KW - EGFR
KW - IGF-1R
KW - Immunoliposomes
KW - Nanobody
UR - http://www.scopus.com/inward/record.url?scp=84861101022&partnerID=8YFLogxK
U2 - 10.1016/j.jconrel.2011.12.027
DO - 10.1016/j.jconrel.2011.12.027
M3 - Article
C2 - 22227023
AN - SCOPUS:84861101022
VL - 159
SP - 281
EP - 289
JO - Journal of controlled release
JF - Journal of controlled release
SN - 0168-3659
IS - 2
ER -