Di Venosa Gabriela, Perotti Christian, Batlle Alcira, Casas Adriana
Centro de Investigaciones sobre Porfirinas y Porfirias (CIPYP). CONICET and Hospital de Clínicas José de San Martín, University of Buenos Aires, Córdoba 2351 1er subsuelo, Ciudad Autónoma de Buenos Aires, CP1120AAF, Argentina.
Photochem Photobiol Sci. 2015 Aug;14(8):1451-64. doi: 10.1039/c4pp00445k. Epub 2015 Apr 2.
It is known that Photodynamic Therapy (PDT) induces changes in the cytoskeleton, the cell shape, and the adhesion properties of tumour cells. In addition, these targets have also been demonstrated to be involved in the development of PDT resistance. The reversal of PDT resistance by manipulating the cell adhesion process to substrata has been out of reach. Even though the existence of cell adhesion-mediated PDT resistance has not been reported so far, it cannot be ruled out. In addition to its impact on the apoptotic response to photodamage, the cytoskeleton alterations are thought to be associated with the processes of metastasis and invasion after PDT. In this review, we will address the impact of photodamage on the microfilament and microtubule cytoskeleton components and its regulators on PDT-treated cells as well as on cell adhesion. We will also summarise the impact of PDT on the surviving and resistant cells and their metastatic potential. Possible strategies aimed at taking advantage of the changes induced by PDT on actin, tubulin and cell adhesion proteins by targeting these molecules will also be discussed.
众所周知,光动力疗法(PDT)会引起肿瘤细胞的细胞骨架、细胞形态和黏附特性发生变化。此外,这些靶点也已被证明与PDT耐药性的产生有关。通过操纵细胞与基质的黏附过程来逆转PDT耐药性一直难以实现。尽管到目前为止尚未报道细胞黏附介导的PDT耐药性的存在,但也不能排除这种可能性。除了对光损伤的凋亡反应有影响外,细胞骨架的改变还被认为与PDT后的转移和侵袭过程有关。在这篇综述中,我们将探讨光损伤对微丝和微管细胞骨架成分及其调节剂在PDT处理细胞以及细胞黏附方面的影响。我们还将总结PDT对存活和耐药细胞及其转移潜能的影响。针对这些分子,利用PDT对肌动蛋白、微管蛋白和细胞黏附蛋白诱导的变化的可能策略也将进行讨论。