Melatonin Research Group, Faculty of Pharmaceutical Sciences, Khon Kaen University, Khon Kaen, 40002, Thailand.
Cell Prolif. 2015 Feb;48(1):67-77. doi: 10.1111/cpr.12158.
Melatonin produces anti-cancer effects via several mechanisms, including by induction of apoptosis. In this way, it has been shown to be of use, in combination with chemotherapeutic drugs, for cancer treatment. The study described here has evaluated effects of melatonin on cytotoxicity, apoptosis and cell cycle arrest induced with the chemotherapeutic agent cisplatin, in human lung adenocarcinoma cisplatin-sensitive cell line (SK-LU-1), which previously had only limit data.
Cells of the SK-LU-1 line were treated with melatonin alone at 1-5 mM concentration or cisplatin alone 10-200 μM, for 48 h in culture. Cytotoxicity was measured by MTT reduction assay. Apoptosis induction was detected by annexin V/PI staining using flow cytometric analysis and DAPI nuclear staining. Change in mitochondrial membrane potential (ΔΨm) was quantified using DiOC6(3) reagent and activities of caspases-3/7 were also investigated. DNA fractions were measured using propidium iodide (PI) staining.
Melatonin or cisplatin alone had 50% (IC50 ) cytotoxicity at 5 mM or 34 μM concentrations respectively. Combination of 1 or 2 mM melatonin and cisplatin significantly augmented cytotoxicity of cisplatin by reducing its IC50 to 11 and 4 μM, respectively. Consistently, combined treatment increased population of apoptotic cells by elevating mitochondrial membrane depolarization, activating caspases-3/7 and inducing cell cycle arrest in the S phase, compared to treatment with cisplatin alone.
These data demonstrate that melatonin enhanced cisplatin-induced cytotoxicity and apoptosis in SK-LU-1 lung cancer cells. SK-LU-1 cell population growth inhibition was mediated by cell cycle arrest in the S phase. These findings suggest that melatonin has the potential to be used for NSCLC treatment in combination with a chemotherapeutic agent such as cisplatin.
褪黑素通过多种机制产生抗癌作用,包括诱导细胞凋亡。通过这种方式,它已被证明与化疗药物联合使用对癌症治疗有用。本研究评估了褪黑素对人肺腺癌细胞顺铂敏感株(SK-LU-1)中化疗药物顺铂诱导的细胞毒性、细胞凋亡和细胞周期阻滞的影响,而此前该细胞株仅有有限的数据。
将 SK-LU-1 细胞株用褪黑素单独处理浓度为 1-5 mM 或顺铂单独处理浓度为 10-200 μM,在培养 48 小时。通过 MTT 还原试验测量细胞毒性。通过流式细胞术分析和 DAPI 核染色检测 Annexin V/PI 染色诱导的细胞凋亡。使用 DiOC6(3) 试剂定量测定线粒体膜电位(ΔΨm),还研究了 caspase-3/7 的活性。使用碘化丙啶(PI)染色测量 DNA 片段。
褪黑素或顺铂单独处理时,50%(IC50)的细胞毒性浓度分别为 5 mM 或 34 μM。1 或 2 mM 褪黑素和顺铂联合处理显著降低了顺铂的 IC50,分别降至 11 和 4 μM,从而显著增强了顺铂的细胞毒性。与单独用顺铂处理相比,联合治疗通过提高线粒体膜去极化、激活 caspase-3/7 和诱导 S 期细胞周期阻滞,增加了凋亡细胞的数量。
这些数据表明,褪黑素增强了 SK-LU-1 肺癌细胞中顺铂诱导的细胞毒性和细胞凋亡。SK-LU-1 细胞群体生长抑制是通过 S 期细胞周期阻滞介导的。这些发现表明,褪黑素有可能与顺铂等化疗药物联合用于 NSCLC 的治疗。