VRR Institute of Biomedical Sciences, Kattupakkam, Chennai 600056, India.
Rumbaugh-Goodwin Institute for Cancer Research, Nova Southeastern University, Ft. Lauderdale, FL 33314, USA.
Cells. 2018 Dec 22;8(1):8. doi: 10.3390/cells8010008.
Gene expression is often altered by epigenetic modifications that can significantly influence the growth ability and progression of cancers. SAHA (Suberoylanilide hydroxamic acid, also known as Vorinostat), a well-known Histone deacetylase (HDAC) inhibitor, can stop cancer growth and metastatic processes through epigenetic alterations. On the other hand, Letrozole is an aromatase inhibitor that can elicit strong anti-cancer effects on breast cancer through direct and indirect mechanisms. A newly developed inhibitor, RG7388 specific for an oncogene-derived protein called MDM2, is in clinical trials for the treatment of various cancers. In this paper, we performed assays to measure the effects of cell cycle arrest resulting from individual drug treatments or combination treatments with SAHA + letrozole and SAHA + RG7388, using the MCF-7 breast cancer cells. When SAHA was used individually, or in combination treatments with RG7388, a significant increase in the cytotoxic effect was obtained. Induction of cell cycle arrest by SAHA in cancer cells was evidenced by elevated p21 protein levels. In addition, SAHA treatment in MCF-7 cells showed significant up-regulation in phospho-RIP3 and MLKL levels. Our results confirmed that cell death caused by SAHA treatment was primarily through the induction of necroptosis. On the other hand, the RG7388 treatment was able to induce apoptosis by elevating BAX levels. It appears that, during combination treatments, with SAHA and RG7388, two parallel pathways might be induced simultaneously, that could lead to increased cancer cell death. SAHA appears to induce cell necroptosis in a p21-dependent manner, and RG7388 seems to induce apoptosis in a p21-independent manner, outlining differential mechanisms of cell death induction. However, further studies are needed to fully understand the intracellular mechanisms that are triggered by these two anti-cancer agents.
基因表达常常受到表观遗传修饰的影响,这些修饰会显著影响癌症的生长能力和进展。SAHA(丁酸钠羟肟酸,也称为伏立诺他)是一种已知的组蛋白去乙酰化酶(HDAC)抑制剂,可通过表观遗传改变来阻止癌症生长和转移过程。另一方面,来曲唑是一种芳香酶抑制剂,可通过直接和间接机制对乳腺癌产生强烈的抗癌作用。一种新开发的抑制剂 RG7388 特异性针对一种称为 MDM2 的癌基因衍生蛋白,正在临床试验中用于治疗各种癌症。在本文中,我们使用 MCF-7 乳腺癌细胞进行了测定,以测量单独使用药物或与 SAHA+来曲唑和 SAHA+RG7388 联合治疗导致的细胞周期停滞的效果。当单独使用 SAHA 或与 RG7388 联合治疗时,获得了显著增加的细胞毒性作用。SAHA 在癌细胞中诱导细胞周期停滞的证据是 p21 蛋白水平升高。此外,SAHA 处理 MCF-7 细胞显示磷酸化 RIP3 和 MLKL 水平显著上调。我们的结果证实,SAHA 处理引起的细胞死亡主要是通过诱导坏死性凋亡。另一方面,RG7388 处理能够通过提高 BAX 水平诱导细胞凋亡。似乎在 SAHA 和 RG7388 的联合治疗中,两种平行途径可能同时被诱导,从而导致癌细胞死亡增加。SAHA 似乎以 p21 依赖的方式诱导细胞坏死性凋亡,而 RG7388 似乎以 p21 非依赖的方式诱导细胞凋亡,阐明了细胞死亡诱导的不同机制。然而,需要进一步研究来充分了解这两种抗癌药物触发的细胞内机制。