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Lactiplantibacillus plantarum Induces Apoptosis in Melanoma and Breast Cancer Cells

细胞凋亡 膜联蛋白 癌症研究 下调和上调 活力测定 免疫印迹 癌症 聚ADP核糖聚合酶 细胞培养 黑色素瘤 医学 生物 内科学 聚合酶 生物化学 遗传学 基因
作者
Oana Budu,Alexandra Mioc,Codruţa Şoica,Florina Căruntu,Andreea Milan,Camelia Oprean,Daniel Lighezan,Slavița Rotunjanu,Viviana Ivan,Christian Banciu
出处
期刊:Microorganisms [Multidisciplinary Digital Publishing Institute]
卷期号:12 (1): 182-182 被引量:1
标识
DOI:10.3390/microorganisms12010182
摘要

Despite the notable advancements witnessed in the past decade in medical and health research domain, cancer remains a prominent global cause of mortality. Moreover, the conventional treatments employed to combat this disease have been found to considerably compromise the quality of life experienced by patients due to its severe side effects. Recent in vitro studies revealed encouraging findings on the potential beneficial effects of probiotics as adjuvants of anticancer therapy, and even as possible agents for the prevention and treatment of various types of malignancies. From this standpoint, the primary objective of this work was to investigate the anticancer properties of Lactiplantibacillus plantarum (LP) and elucidate its underlying mechanism of action. In order to investigate this matter, several doses of LP (ranging from 105 to 1010 CFU/mL) were examined in relation to melanoma cancer cell lines (A375) and breast cancer cell line (MCF-7). The cell viability findings, which were substantiated by morphological investigations and annexin V/PI assay, indicated that LP exerted inhibitory effects on cellular activity and triggered apoptosis. Additionally, upon further investigation into its mechanism, it was observed through the apoptosis assay and Western blot analysis that the administration of LP resulted in an elevation of pro-apoptotic BAX protein levels and an upregulation of cleaved poly-ADP-ribose polymerase (PARP) protein expression. Conversely, the levels of anti-apoptotic Bcl-2 protein were found to decrease in the A375 and MCF-7 cell lines. These findings provide insight into the pro-apoptotic mechanism of action of LP in these specific cell lines.

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