Andrographolide Reverses Doxorubicin Resistance in Human Breast Cancer Stem Cells by Regulating Apoptotic Gene Expressions

Septelia Inawati Wanandi, Resda Akhra Syahrani, Ayu Suraduhita, Elvira Yunita, Melva Louisa
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Abstract

BACKGROUND: Breast cancer stem cells (BCSCs) have been identified as playing a crucial role in therapeutic resistance. This resistance can be attributed to the anti-apoptotic protein survivin and the antioxidant MnSOD high expression. To overcome the resistance to doxorubicin (DOX), this study proposed the utilization of andrographolide (ANDRO), the primary bioactive compound in Andrographis paniculata leaves. The objective was to examine the role of andrographolide in regulating survivin, caspase-9, and caspase-3 gene expressions to reverse doxorubicin resistance in human BCSCs.METHODS: BCSCs were exposed to 0.1 µM DOX every two days or 50 µM rotenone (ROT) for 6 hours, subsequently supplemented with 0.3 mM ANDRO. Superoxide and peroxide levels were measured using DHE and DCFH-DA assay. The MnSOD, survivin, caspase-9, and caspase-3 mRNA expression levels were analyzed using qRT-PCR. Protein expressions were evaluated using Western blotting assay. MnSOD activity was determined using xanthine oxidase inhibition assay. The apoptotic cells were determined using Annexin-V/PI staining.RESULTS: This study indicated that the cytotoxic mechanisms of DOX, similar to ROT, in BCSCs were attributed to oxidative stress, as evidenced by an elevation in superoxide rather than peroxide levels, accompanied by a decrease in MnSOD activity. This study also highlighted that ANDRO reversed DOX resistance in BCSCs subjected to repeated DOX treatment by downregulating survivin and upregulating caspase-9 and caspase-3 mRNA expressions, thereby activating the intrinsic apoptotic pathway.CONCLUSION: This study provides insights into the role of ANDRO in modulating the expression of apoptotic genes, such as survivin, caspase-9, and caspase-3, to overcome DOX resistance in BCSCs.KEYWORDS: breast cancer, breast cancer stem cell, andrographolide, doxorubicin, oxidative stress, apoptosis
穿心莲内酯通过调节凋亡基因表达逆转人乳腺癌干细胞对阿霉素的耐药性
背景:乳腺癌干细胞(BCSCs)在治疗耐药中起着至关重要的作用。这种抗性可归因于抗凋亡蛋白survivin和抗氧化剂MnSOD的高表达。为了克服对多柔比星(DOX)的耐药性,本研究提出利用穿心莲叶片中的主要生物活性物质穿心莲内酯(andrographolide, ANDRO)。目的是研究穿心莲内酯在调节survivin、caspase-9和caspase-3基因表达以逆转人bscs中阿霉素耐药性中的作用。方法:将BCSCs每两天暴露于0.1µM DOX或50µM鱼藤酮(ROT)中6小时,随后补充0.3 mM ANDRO。采用DHE和DCFH-DA法测定超氧化物和过氧化物水平。采用qRT-PCR分析MnSOD、survivin、caspase-9、caspase-3 mRNA表达水平。Western blotting法检测蛋白表达。采用黄嘌呤氧化酶抑制法测定MnSOD活性。Annexin-V/PI染色检测凋亡细胞。结果:本研究表明,与ROT类似,DOX在BCSCs中的细胞毒性机制归因于氧化应激,这可以通过超氧化物水平升高而不是过氧化物水平升高来证明,同时伴有MnSOD活性降低。本研究还强调,ANDRO通过下调survivin和上调caspase-9和caspase-3 mRNA表达,逆转了反复DOX处理的BCSCs对DOX的耐药,从而激活了内在凋亡通路。结论:本研究揭示了ANDRO通过调节凋亡基因survivin、caspase-9和caspase-3的表达来克服BCSCs对DOX的耐药。关键词:乳腺癌,乳腺癌干细胞,穿心莲内酯,阿霉素,氧化应激,细胞凋亡
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