Koronowicz Aneta, Krawczyk Katarzyna, Such Aleksandra, Piasna-Słupecka Ewelina, Drozdowska Mariola, Leszczyńska Teresa
Department of Human Nutrition and Dietetics, Faculty of Food Technology, University of Agriculture in Krakow, 30-149 Krakow, Poland.
Nutrients. 2024 Dec 12;16(24):4287. doi: 10.3390/nu16244287.
BACKGROUND/OBJECTIVES: Melanoma malignum is considered the most dangerous form of skin cancer, characterized by the exceptional resistance to many conventional chemotherapies. The aim of this study was to evaluate the effect of Nutramil Complex (NC)-Food for Special Medical Purpose (FSMP), on two types of melanoma cell lines, primary WM115 and malignant WM266-4.
At 24 h after seeding, growth medium was replaced with a medium containing encoded treatments of NC or NC-CC (Nutramil Complex without calcium caseinate) at various concentrations. Cells were treated for 24, 48, and 72 h.
Our results showed that Nutramil Complex reduces proliferation of malignant melanoma WM266-4 cells but did not affect the proliferation of WM115 primary melanoma. This was followed by measured down-regulation of selected pro-survival proteins expression in WM266-4 cells, specifically ERK1/2, AKT-1, HSP27, Survivin, and TAK1. Interestingly, our results showed elevated levels of some pro-apoptotic proteins in both cell lines, including Bad, Smad2, p38MAPK, cleaved forms of Caspase-3/7, as well as cleaved PARP.
Taken together, our results indicate that various melanoma cancer cell lines may respond in a different way to the same compound. They also suggest induction of apoptotic pathway by Nutramil Complex as the most likely mechanism of its anticarcinogenic activity.
背景/目的:恶性黑色素瘤被认为是最危险的皮肤癌形式,其特点是对许多传统化疗具有极强的耐药性。本研究的目的是评估特殊医学用途食品Nutramil Complex(NC)对两种黑色素瘤细胞系,即原发性WM115和恶性WM266 - 4的影响。
接种24小时后,将生长培养基替换为含有不同浓度NC或NC - CC(不含酪蛋白钙的Nutramil Complex)编码处理的培养基。细胞处理24、48和72小时。
我们的结果表明,Nutramil Complex可降低恶性黑色素瘤WM266 - 4细胞的增殖,但不影响WM115原发性黑色素瘤细胞的增殖。随后检测到WM266 - 4细胞中某些促生存蛋白表达下调,特别是ERK1/2、AKT - 1、HSP27、Survivin和TAK1。有趣的是,我们的结果显示两种细胞系中一些促凋亡蛋白水平升高,包括Bad、Smad2、p38MAPK、Caspase - 3/7的裂解形式以及裂解的PARP。
综上所述,我们的结果表明不同的黑色素瘤癌细胞系可能对同一化合物有不同反应。它们还提示Nutramil Complex诱导凋亡途径是其抗癌活性最可能的机制。