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藏红花酸通过诱导多发性骨髓瘤细胞(RPMI8226)线粒体功能障碍抑制细胞增殖并诱导细胞凋亡。

Habb-e-Asgandh Suppresses Cell Proliferation and Induces Apoptosis through Mitochondria Dysfunction in Multiple Myeloma Cells (RPMI8226).

机构信息

Department of Biochemistry, All India Institute of Medical Sciences, New Delhi, India.

出版信息

Asian Pac J Cancer Prev. 2022 Nov 1;23(11):3629-3639. doi: 10.31557/APJCP.2022.23.11.3629.

Abstract

OBJECTIVE

This study was conducted to assess the anti-neoplastic properties of Habb-e-Asgandh in multiple myeloma cells (RPMI8226).

METHODS

Multiple myeloma cells (RPMI8226) were cultured according to the ATCC's instruction. The anti-proliferative effect of HeA was assessed by MTT assay and proliferating cellnuclear antigen (PCNA) activity. Cell cycle analysis, cellular apoptosis, and mitochondria membrane potential analysis was done by flow cytometry. Total antioxidants, migratory potential, angiogenesis and inflammatory biomarkers were also estimated after treatment of RPMI8226 with HeA.

RESULTS

LD30 and LD50 dose of HeA was 0.3mg/ml and 0.5mg/ml respectively determined by MTT assay and also confirmed by a reduced PCNA activity. Cell cycle analysis of RPMI8226 cells revealed that sub-G0/G1 phase increases upon treatment with HeA alone or in combination with lenalidomide. Annexin V-FITC/PI is used to detect early apoptosis, late apoptosis and necrotic cells and results showed that percentage of apoptotic cells increased in RPMI8226 cells after treatment with HeA. Also, HeA induces loss of mitochondria membrane potential (MMP) in MM cells in-vitro as measured by cationic JC1 dye staining. Upon treatment, the abnormal overexpression of oncogenic protein, AKT serine/threonine kinase has also been reduced. Furthermore, anti-oxidants level also increased while migratory potential, angiogenesis and inflammation decreased in multiple myeloma cell line upon treatment with HeA.

CONCLUSION

Collectively, our results demonstrated that integrative therapy of habb-e-asgandh efficiently eliminates the need to use higher dose of lenalidomide for multiple myeloma treatment.

摘要

目的

本研究旨在评估哈巴-阿斯甘德(Habb-e-Asgandh)在多发性骨髓瘤细胞(RPMI8226)中的抗肿瘤特性。

方法

根据 ATCC 的说明培养多发性骨髓瘤细胞(RPMI8226)。通过 MTT assay 和增殖细胞核抗原(PCNA)活性评估 HeA 的抗增殖作用。通过流式细胞术进行细胞周期分析、细胞凋亡、线粒体膜电位分析。在用 HeA 处理 RPMI8226 后,还评估了总抗氧化剂、迁移潜力、血管生成和炎症生物标志物。

结果

通过 MTT assay 确定 HeA 的 LD30 和 LD50 剂量分别为 0.3mg/ml 和 0.5mg/ml,PCNA 活性降低也证实了这一点。RPMI8226 细胞的细胞周期分析表明,单独或与来那度胺联合使用 HeA 后,sub-G0/G1 期增加。Annexin V-FITC/PI 用于检测早期凋亡、晚期凋亡和坏死细胞,结果表明 HeA 处理后 RPMI8226 细胞中凋亡细胞的比例增加。此外,HeA 在体外诱导 MM 细胞中线粒体膜电位(MMP)丧失,如阳离子 JC1 染料染色所示。在用 HeA 治疗后,异常过表达的致癌蛋白 AKT 丝氨酸/苏氨酸激酶也减少。此外,在用 HeA 处理多发性骨髓瘤细胞系时,抗氧化剂水平增加,迁移潜力、血管生成和炎症减少。

结论

总之,我们的研究结果表明,哈巴-阿斯甘德的综合治疗有效地消除了多发性骨髓瘤治疗中需要使用更高剂量来那度胺的需求。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/57fe/9930948/1c74e27e4e58/APJCP-23-3629-g001.jpg

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