Reversing multidrug resistance in breast cancer cells by silencing ABC transporter genes with nanoparticle-facilitated delivery of target siRNAs

• Published in: International journal of nanomedicine 2012, Vol.7 (default), p.2473-2481
• Main Authors: Li, Yong Tsuey, Chua, Ming Jang, Kunnath, Anil Philip, Chowdhury, Ezharul Hoque
• Format: Article
• Language: English
• Subjects: ABC transporter; ABC transporters; Apatites - pharmacokinetics; Apatites - pharmacology; ATP-Binding Cassette Transporters - genetics; ATP-Binding Cassette Transporters - metabolism; Breast cancer; Breast Neoplasms - drug therapy; Breast Neoplasms - genetics; Breast Neoplasms - metabolism; Breast Neoplasms - therapy; carbonate apatite; Cell Line, Tumor; chemosensitivity; Combined Modality Therapy; Dose-Response Relationship, Drug; Drug Carriers - pharmacokinetics; Drug Carriers - pharmacology; Drug Resistance, Multiple; Drug Resistance, Neoplasm; Female; Gene expression; Gene Silencing - drug effects; Humans; MCF-7 Cells; multidrug resistance; Multidrug resistant organisms; Nanoparticles - chemistry; Original Research; RNA, Small Interfering - administration & dosage; RNA, Small Interfering - genetics; RNA, Small Interfering - pharmacokinetics; siRNA; transfection
• ISSN: 1178-2013; 1176-9114; 1178-2013
• DOI: 10.2147/IJN.S30500

Multidrug resistance, a major impediment to successful cancer chemotherapy, is the result of overexpression of ATP-binding cassette (ABC) transporters extruding internalized drugs. Silencing of ABC transporter gene expression with small interfering RNA (siRNA) could be an attractive approach to overcome multidrug resistance of cancer, although delivery of siRNA remains a major hurdle to fully exploit the potential of siRNA-based therapeutics. Recently, we have developed pH-sensitive carbonate apatite nanoparticles to efficiently carry and transport siRNA across the cell membrane, enabling knockdown of the cyclin B1 gene and consequential induction of apoptosis in synergy with anti-cancer drugs. We report that carbonate apatite-mediated delivery of the siRNAs targeting ABCG2 and ABCB1 gene transcripts in human breast cancer cells which constitutively express both of the transporter genes dose-dependently enhanced chemosensitivity to doxorubicin, paclitaxel and cisplatin, the traditionally used chemotherapeutic agents. Moreover, codelivery of two specific siRNAs targeting ABCB1 and ABCG2 transcripts resulted in a more robust increase of chemosensitivity in the cancer cells, indicating the reversal of ABC transporter-mediated multidrug resistance. The delivery concept of multiple siRNAs against ABC transporter genes is highly promising for preclinical and clinical investigation in reversing the multidrug resistance phenotype of breast cancer.