Aniogo Eric Chekwube, Plackal Adimuriyil George Blassan, Abrahamse Heidi
Laser Research Centre, Faculty of Health Sciences, University of Johannesburg, P.O. Box 17011, Doornfontein, Johannesburg, 2028 South Africa.
Cancer Cell Int. 2019 Apr 11;19:91. doi: 10.1186/s12935-019-0815-0. eCollection 2019.
Breast cancer heterogeneity allows cells with different phenotypes to co-exist, contributing to treatment failure and development of drug resistance. In addition, abnormal signal transduction and dysfunctional DNA repair genes are common features with breast cancer resistance. Chemo-resistance of breast cancer associated with multidrug resistance events utilizes ATP-binding cassette (ABC) efflux transporters to decrease drug intracellular concentration. Photodynamic therapy (PDT) is the treatment that involves a combination of a photosensitizer (PS), light and molecular oxygen to induce cell death. This treatment modality has been considered as a possible approach in combatting multidrug resistance phenomenon although its therapeutic potential towards chemo-resistance is still unclear. Attempts to minimize the impact of efflux transporters on drug resistance suggested concurrent use of chemotherapy agents, nanotechnology, endolysosomal release of drug by photochemical internalization and the use of structurally related compound inhibitors to block the transport function of the multidrug resistant transporters. In this review, we briefly summarize the role of membrane ABC efflux transporters in therapeutic outcomes and highlight research findings related to PDT and its applications on breast cancer with multidrug resistance phenotype. With the development of an ideal PS for photodynamic cancer treatment, it is possible that light activation may be used not only to sensitize the tumour but also to enable release of PS into the cytosol and as such bypass efflux membrane proteins and inhibit escape pathways that may lead to resistance.
乳腺癌的异质性使得具有不同表型的细胞能够共存,这导致治疗失败和耐药性的产生。此外,异常的信号转导和功能失调的DNA修复基因是乳腺癌耐药的常见特征。与多药耐药事件相关的乳腺癌化疗耐药利用ATP结合盒(ABC)外排转运蛋白来降低药物细胞内浓度。光动力疗法(PDT)是一种涉及光敏剂(PS)、光和分子氧联合作用以诱导细胞死亡的治疗方法。尽管其对化疗耐药的治疗潜力仍不明确,但这种治疗方式已被视为对抗多药耐药现象的一种可能方法。为尽量减少外排转运蛋白对耐药性的影响,人们尝试同时使用化疗药物、纳米技术、通过光化学内化实现药物的溶酶体释放以及使用结构相关的化合物抑制剂来阻断多药耐药转运蛋白的转运功能。在本综述中,我们简要总结了膜ABC外排转运蛋白在治疗结果中的作用,并重点介绍了与PDT及其在具有多药耐药表型的乳腺癌中的应用相关的研究发现。随着用于光动力癌症治疗的理想PS的开发,光激活不仅有可能用于使肿瘤敏感化,还能使PS释放到细胞质中,从而绕过外排膜蛋白并抑制可能导致耐药的逃逸途径。