Cyclooxygenase-2
(COX-2) is highly expressed in many different cancers; particularly in
colorectal cancer (CRC). Liposomal drug delivery systems can be used to
increase the therapeutic efficacy of CLX while minimizing its side effects.
Cetuximab (anti-Epidermal Growth Factor Receptor -EGFR- monoclonal antibody) is
a promising targeting ligand since EGFR is highly expressed in a wide range of
solid tumors. Dual targeting of EGFR and COX-2 signaling may have additive or
synergistic effects. Here, we describe an EGFR-targeted immunoliposome for
enhancing the delivery of CLX to cancer cells.
Cell association studies indicated that the immunoliposome uptake was
higher in EGFR-overexpressing cells compared to the non-targeted liposomes. In
addition, the CLX-loaded-anti-EGFR immunoliposomes were significantly more
toxic compared to the non-targeted ones in cancer cells with EGFR-overexpression
but not in the cells with low EGFR expression, regardless of their COX-2
expression status. Thus, selective targeting of CLX with anti-EGFR
immunoliposomes appears to be a promising strategy for therapy of tumors that
overexpress EGFR.
BAP-07-02-2014-004 and TÜBA-GEBİP
TARGETING CYCLOOXYGENASE-2 WITH A TARGETED LIPOSOMAL FORMULATION FOR COLORECTAL CANCER.
Bölüm | Articles |
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Yazarlar | |
Yayımlanma Tarihi | 16 Şubat 2017 |
Yayımlandığı Sayı | Yıl 2017 Cilt: Volume 2 Sayı: İssue 1 (1) - 2.İnternational Congress Of Forensic Toxicology |