Faião-Flores Fernanda, Suarez José Agustín Quincoces, Soto-Cerrato Vanessa, Espona-Fiedler Margarita, Pérez-Tomás Ricardo, Maria Durvanei Augusto
Laboratory of Biochemistry and Biophysics, Butantan Institute, 1500 Vital Brasil Avenue, São Paulo, 05503-900, Brazil.
Tumour Biol. 2013 Apr;34(2):1235-43. doi: 10.1007/s13277-013-0666-6. Epub 2013 Jan 23.
Melanoma is one of the most aggressive types of skin cancer and its incidence rate is still increasing. All existing treatments are minimally effective. Consequently, new therapeutic agents for melanoma treatment should be developed. The DM-1 compound is a curcumin analog that possesses several curcumin characteristics, such as antiproliferative, antitumor, and anti-metastatic properties. The aim of this study was to evaluate the different signaling pathways involved in the cytotoxic effect of DM-1 on melanoma cells. The apoptotic process and cytoskeletal changes were evaluated by immunoblotting and immunofluorescence, respectively, in melanoma cells. After DM-1 treatment, SK-MEL-5 melanoma cells showed actin filament disorganization with spicule formation throughout the cytoskeleton and significant reduction of focal adhesion as well as they were present only at cell extremities, conferring a poor connection between the cell and the substrate. Besides this, there was significant filopodium retraction and loss of typical cytoskeleton scaffold. These modifications contributed to cell detachment followed by cell death. Furthermore, DM-1-induced apoptosis was triggered by multiple Bcl-2 proteins involved in both the extrinsic and the intrinsic apoptotic pathways. SK-MEL-5 cells showed a death mechanism mainly by Bcl-2/Bax ratio decrease, whereas A375 cells presented apoptosis induction by Mcl-1 and Bcl-xL downregulation. In SK-MEL-5 and A375 melanoma cells, there was a significant increase in the active form of caspase 9, and the inactive form of the effector caspase 3 was decreased in both cell lines. Expression of cleaved poly ADP ribose polymerase was increased after DM-1 treatment in these melanoma cell lines, demonstrating that the apoptotic process occurred. Altogether, these data elucidate the cellular and molecular mechanisms involved in the cytotoxicity induced by the antitumor agent DM-1 in melanoma cells.
黑色素瘤是最具侵袭性的皮肤癌类型之一,其发病率仍在上升。所有现有的治疗方法效果都很有限。因此,应开发用于治疗黑色素瘤的新型治疗药物。DM-1化合物是一种姜黄素类似物,具有多种姜黄素特性,如抗增殖、抗肿瘤和抗转移特性。本研究的目的是评估DM-1对黑色素瘤细胞的细胞毒性作用所涉及的不同信号通路。分别通过免疫印迹和免疫荧光评估黑色素瘤细胞中的凋亡过程和细胞骨架变化。用DM-1处理后,SK-MEL-5黑色素瘤细胞显示肌动蛋白丝紊乱,整个细胞骨架形成针状物,粘着斑显著减少,且仅存在于细胞末端,导致细胞与基质之间的连接不良。除此之外,丝状伪足明显回缩,典型的细胞骨架支架丧失。这些改变导致细胞脱离,随后细胞死亡。此外,DM-1诱导的凋亡由参与外源性和内源性凋亡途径的多种Bcl-2蛋白触发。SK-MEL-5细胞主要通过Bcl-2/Bax比值降低表现出死亡机制,而A375细胞通过Mcl-1和Bcl-xL下调诱导凋亡。在SK-MEL-5和A375黑色素瘤细胞中,caspase 9的活性形式显著增加,效应caspase 3的无活性形式在两种细胞系中均降低。在这些黑色素瘤细胞系中,DM-1处理后裂解的聚ADP核糖聚合酶的表达增加,表明凋亡过程发生。总之,这些数据阐明了抗肿瘤药物DM-1在黑色素瘤细胞中诱导细胞毒性所涉及的细胞和分子机制。