收稿日期: 2024-08-01
网络出版日期: 2024-12-16
基金资助
国家自然科学基金项目(81560026);江西省中医药管理局科技计划课题(2022B783)
The inhibitory effect and molecular mechanism of 6-gingerol on human multiple myeloma cells
Received date: 2024-08-01
Online published: 2024-12-16
目的 研究6-姜辣素对人多发性骨髓瘤细胞的抑制作用及分子机制。 方法 体外培养人多发性骨髓瘤RPMI 8226、ARH77细胞,加入不同浓度(50、100、200、300、400 μmol/L)的6-姜辣素处理RPMI 8226、ARH77 细胞,CCK-8法测定细胞增殖抑制率;流式细胞术检测细胞凋亡和周期;qRT-PCR和Western blotting法检测基因和蛋白表达水平。 结果 6-姜辣素以剂量和时间依赖的方式抑制RPMI 8226、ARH77细胞的增殖,并诱导其凋亡,差异有统计学意义(P < 0.05);进一步机制研究发现6-姜辣素处理RPMI 8226细胞后,将细胞阻滞在G0/G1期,显著增加Bax mRNA水平,降低Bcl-2 mRNA和c-Myc mRNA的水平(P < 0.05);同时显著增加Bax、Cleaved-PARP、Cleaved-caspase3、P53、p-AKT蛋白的表达,而降低Bcl-2蛋白的表达(P < 0.05)。 结论 6-姜辣素可抑制MM细胞增殖及诱导其凋亡,并阻滞细胞周期在G0/G1期,其机制可能与抑制AKT信号通路并通过影响 Bcl-2家族蛋白表达以及c-Myc表达受抑等密切有关。
孔春芳 , 李安娜 , 柯波 , 丁伟荣 , 刘婷婷 , 符环 , 张婷婷 , 金成豪 , 吴美 . 6-姜辣素对人多发性骨髓瘤细胞的抑制作用及分子机制[J]. 实用医学杂志, 2024 , 40(23) : 3291 -3297 . DOI: 10.3969/j.issn.1006-5725.2024.23.003
Objective To investigate the inhibitory effect and elucidate the molecular mechanism of 6?gingerol on human multiple myeloma cells. Methods The human multiple myeloma cell lines RPMI 8226 and ARH77 were cultured in vitro, followed by treatment with varying concentrations (50, 100, 200, 300, 400 μmol/L) of 6?gingerol. The inhibitory effect on cell proliferation was assessed using the CCK?8 assay. Flow cytometry was employed to evaluate cell apoptosis and cycle distribution. Additionally, qRT?PCR and Western blotting techniques were utilized to analyze gene and protein expression levels. Results The proliferation of RPMI 8226 and ARH77 cells was dose? and time?dependently inhibited by 6?gingerol, leading to the induction of apoptosis with statistically significant differences (P < 0.05). Further mechanistic investigations revealed that treatment with 6?gingerol arrested RPMI 8226 cells in the G0/G1 phase, resulting in a significant increase in Bax levels and a decrease in Bcl?2 mRNA and c?Myc mRNA levels (P < 0.05). Additionally, it significantly upregulated the expression of Bax, Cleaved?PARP, Cleaved?caspase3, P53, and p?AKT proteins while down regulating the expression of Bcl?2 protein (P < 0.05). Conclusions The compound 6?Gingerol exhibits inhibitory effects on the proliferation and induction of apoptosis in MM cells, as well as cell cycle arrest at the G0/G1 phase. Its mechanism of action is likely associated with the suppression of the AKT signaling pathway, downregulation of Bcl?2 family protein expression, and inhibition of c?Myc expression.
Key words: multiple myeloma; 6-gingerol; cell proliferation; cell apoptosis; signal pathway
| 1 | FAZIO M, DEL FABRO V, PARRINELLO N L, et al. Multiple myeloma in 2023 ways: From trials to real life [J]. Curr Oncol, 2023, 30(11): 9710-9733. doi:10.3390/curroncol30110705 |
| 2 | GARFALL A L. New biological therapies for multiple myeloma [J]. Annu Rev Med, 2024, 75: 13-29. doi:10.1146/annurev-med-050522-033815 |
| 3 | SIEGEL R L, MILLER K D, FUCHS H E, et al. Cancer statistics, 2022 [J]. CA Cancer J Clin, 2022, 72(1): 7-33. doi:10.3322/caac.21708 |
| 4 | WU S, ZHU J, WU G, et al. 6-Gingerol alleviates ferroptosis and inflammation of diabetic cardiomyopathy via the Nrf2/HO-1 Pathway [J]. Oxid Med Cell Longev, 2022, 2022: 3027514. doi:10.1155/2022/3027514 |
| 5 | TSAI Y, XIA C, SUN Z. The Inhibitory effect of 6-Gingerol on ubiquitin-specific peptidase 14 enhances autophagy-dependent ferroptosis and anti-tumor in vivo and in vitro [J]. Front Pharmacol, 2020, 11: 598555. doi:10.3389/fphar.2020.598555 |
| 6 | BHASKAR A, KUMARI A, SINGH M, et al. [6]-Gingerol exhibits potent anti-mycobacterial and immunomodulatory activity against tuberculosis [J]. Int Immunopharmacol, 2020, 87: 106809. doi:10.1016/j.intimp.2020.106809 |
| 7 | HAN J J, LI X, YE Z Q, et al. Treatment with 6-Gingerol regulates dendritic cell activity and ameliorates the severity of experimental autoimmune encephalomyelitis [J]. Mol Nutr Food Res, 2019, 63(18): e1801356. doi:10.1002/mnfr.201801356 |
| 8 | LI A, ZHAO M, YANG Z, et al. 6-Gingerol alleviates placental injury in preeclampsia by inhibiting oxidative stress via BNIP3/LC3 signaling-mediated trophoblast mitophagy [J]. Front Pharmacol, 2023, 14: 1243734. doi:10.3389/fphar.2023.1243734 |
| 9 | GUNAWAN S, MUNIKA E, WULANDARI E T, et al. 6-gingerol ameliorates weight gain and insulin resistance in metabolic syndrome rats by regulating adipocytokines [J]. Saudi Pharm J, 2023, 31(3): 351-358. doi:10.1016/j.jsps.2023.01.003 |
| 10 | KIM M J, KU J M, CHOI Y J, et al. Reduced HIF-1α Stability Induced by 6-Gingerol Inhibits Lung Cancer Growth through the Induction of Cell Death [J]. Molecules, 2022, 27(7): 2106. doi:10.3390/molecules27072106 |
| 11 | ZHANG H, KIM E, YI J, et al. [6]-Gingerol Suppresses Oral Cancer Cell Growth by Inducing the Activation of AMPK and Suppressing the AKT/mTOR Signaling Pathway [J]. In Vivo, 2021, 35(6): 3193-3201. doi:10.21873/invivo.12614 |
| 12 | CHOI N R, CHOI W G, KWON M J, et al. [6]-Gingerol induces Caspase-Dependent Apoptosis in Bladder Cancer cells via MAPK and ROS Signaling [J]. Int J Med Sci, 2022, 19(7): 1093-1102. doi:10.7150/ijms.73077 |
| 13 | SALARI Z, KHOSRAVI A, POURKHANDANI E, et al. The inhibitory effect of 6-gingerol and cisplatin on ovarian cancer and antitumor activity: In silico, in vitro, and in vivo [J]. Front Oncol, 2023, 13: 1098429. doi:10.3389/fonc.2023.1098429 |
| 14 | AL-ODAT O S, GUIRGUIS D A, SCHMALBACH N K, et al. Autophagy and apoptosis: current challenges of treatment and drug resistance in multiple myeloma [J]. Int J Mol Sci, 2022, 24(1): 644. doi:10.3390/ijms24010644 |
| 15 | CZABOTAR P E, LESSENE G, STRASSER A, et al. Control of apoptosis by the BCL-2 protein family: implications for physiology and therapy [J]. Nat Rev Mol Cell Biol, 2014, 15(1): 49-63. doi:10.1038/nrm3722 |
| 16 | LOPEZ J, TAIT S W. Mitochondrial apoptosis: killing cancer using the enemy within [J]. Br J Cancer, 2015, 112(6): 957-962. doi:10.1038/bjc.2015.85 |
| 17 | DREL V R, SHYMANS'KY? I O, SYBIRNA N O, et al. Role of PARP and protein poly-ADP-ribosylation process in regulation of cell functions [J]. Ukr Biokhim Zh (1999), 2011, 83(6): 5-34. |
| 18 | ZHANG Y, YANG X, ZHOU H, et al. BIBR1532 inhibits proliferation and enhances apoptosis in multiple myeloma cells by reducing telomerase activity [J]. PeerJ, 2023, 11: e16404. doi:10.7717/peerj.16404 |
| 19 | KERROS C, CAVEY T, SOLA B, et al. Somatostatin and opioid receptors do not regulate proliferation or apoptosis of the human multiple myeloma U266 cells [J]. J Exp Clin Cancer Res, 2009, 28(1): 77. doi:10.1186/1756-9966-28-77 |
| 20 | SHEN W, ZHAO Y, CHEN H, et al. M3, a natural lignan xyloside, exhibits potent anticancer activity in HCT116 cells [J]. Oncol Lett, 2019, 17(2): 2117-2122. |
| 21 | ZHANG Y, QIAN J, JIANG M, et al. LTe2 induces cell apoptosis in multiple myeloma by suppressing AKT phosphorylation at Thr308 and Ser473 [J]. Front Oncol, 2023, 13: 1269670. doi:10.3389/fonc.2023.1269670 |
| 22 | SAADOUNE C, NOUADI B, HAMDAOUI H, et al. Multiple Myeloma: Bioinformatic Analysis for Identification of Key Genes and Pathways [J]. Bioinform Biol Insights, 2022, 16: 11779322221115545. doi:10.1177/11779322221115545 |
| 23 | ENGELAND K. Cell cycle regulation: p53-p21-RB signaling [J]. Cell Death Differ, 2022, 29(5): 946-960. doi:10.1038/s41418-022-00988-z |
| 24 | MASSó-VALLéS D, SOUCEK L. Blocking Myc to Treat Cancer: Reflecting on Two Decades of Omomyc [J]. Cells, 2020, 9(4): 883. doi:10.3390/cells9040883 |
| 25 | ADIKESAVAN M, ATHIRAJA P, DIVAKAR M B B. Investigation on the anticancer activity of [6]-gingerol of zingiber officinale and its structural analogs against skin cancer [J]. Curr Comput Aided Drug Des, 2024, 20(4): 367-373. doi:10.2174/1573409919666230418095105 |
| 26 | KHAN H, AZAD I, ARIF Z, et al. Structure based docking and biological evaluation towards exploring potential anti-cancerous and apoptotic activity of 6-Gingerol against human prostate carcinoma cells [J]. BMC Complement Med Ther, 2024, 24(1): 8. doi:10.1186/s12906-023-04269-1 |
| 27 | LI B, ZU M, JIANG A, et al. Magnetic natural lipid nanoparticles for oral treatment of colorectal cancer through potentiated antitumor immunity and microbiota metabolite regulation [J]. Biomaterials, 2024, 307: 122530. doi:10.1016/j.biomaterials.2024.122530 |
| 28 | EDIRIWEERA M K, TENNEKOON K H, SAMARAKOON S R. Role of the PI3K/AKT/mTOR signaling pathway in ovarian cancer: Biological and therapeutic significance [J]. Semin Cancer Biol, 2019, 59: 147-160. doi:10.1016/j.semcancer.2019.05.012 |
| 29 | ISA R, HORINAKA M, TSUKAMOTO T, et al. The Rationale for the Dual-Targeting Therapy for RSK2 and AKT in Multiple Myeloma [J]. Int J Mol Sci, 2022, 23(6): 2919. doi:10.3390/ijms23062919 |
| 30 | LU Q, YANG D, LI H, et al. Multiple myeloma: signaling pathways and targeted therapy [J]. Mol Biomed, 2024, 5(1): 25. doi:10.1186/s43556-024-00188-w |
| 31 | XU S, ZHANG H, LIU T, et al. 6-Gingerol induces cell-cycle G1-phase arrest through AKT-GSK 3β-cyclin D1 pathway in renal-cell carcinoma [J]. Cancer Chemother Pharmacol, 2020, 85(2): 379-390. doi:10.1007/s00280-019-03999-9 |
/
| 〈 |
|
〉 |