Halaby Reginald
Department of Biology, Montclair State University, Montclair, NJ 07043, USA.
Cancer Drug Resist. 2019 Mar 19;2(1):31-42. doi: 10.20517/cdr.2018.23. eCollection 2019.
Chemotherapy remains a primary treatment modality for various malignancies. However, resistance to chemotherapeutic drugs is a major obstacle to curative cancer therapy. Lysosomes are acidic organelles that participate in cellular digestion. However, there is rising interest in lysosomes because of their involvement with cancer. For example, extracellular secretion of lysosomal enzymes promote tumorigenesis; cytosolic leakage of lysosomal hydrolases promote apoptosis; and weak chemotherapeutic bases diffuse across the lysosomal membrane and become entrapped in lysosomes in their cationic state. Lysosomal drug sequestration lowers the cytotoxic potential of chemotherapeutics, reduces drug availability to sites of action, and contributes to cancer resistance. This review examines various mechanisms of lysosomal drug sequestration and their consequences on cancer multidrug resistance. Strategies for overcoming drug resistance by exploiting lysosomes as subcellular targets to reverse drug sequestration and drug resistance are also discussed.
化疗仍然是各种恶性肿瘤的主要治疗方式。然而,对化疗药物的耐药性是根治性癌症治疗的主要障碍。溶酶体是参与细胞消化的酸性细胞器。然而,由于溶酶体与癌症有关,人们对它的兴趣日益增加。例如,溶酶体酶的细胞外分泌促进肿瘤发生;溶酶体水解酶的胞质泄漏促进细胞凋亡;弱化疗碱扩散穿过溶酶体膜并以阳离子状态被困在溶酶体中。溶酶体药物隔离降低了化疗药物的细胞毒性潜力,减少了药物作用位点的可用性,并导致癌症耐药性。本综述探讨了溶酶体药物隔离的各种机制及其对癌症多药耐药性的影响。还讨论了通过利用溶酶体作为亚细胞靶点来逆转药物隔离和耐药性以克服耐药性的策略。