[1]阎 晗,黄 珊.姜黄素对人结直肠癌SW-620细胞抗肿瘤效果的研究[J].天津医科大学学报,2024,30(06):479-483.[doi:10.20135/j.issn.1006-8147.2024.06.0479]
YAN Han,HUANG Shan.Anti-tumor effect of curcumin on human colorectal cancer SW-620 cells[J].Journal of Tianjin Medical University,2024,30(06):479-483.[doi:10.20135/j.issn.1006-8147.2024.06.0479]
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姜黄素对人结直肠癌SW-620细胞抗肿瘤效果的研究(PDF)
《天津医科大学学报》[ISSN:1006-8147/CN:12-1259/R]
- 卷:
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30卷
- 期数:
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2024年06期
- 页码:
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479-483
- 栏目:
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肿瘤疾病专题
- 出版日期:
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2024-11-20
文章信息/Info
- Title:
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Anti-tumor effect of curcumin on human colorectal cancer SW-620 cells
- 文章编号:
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1006-8147(2024)06-0479-06
- 作者:
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阎 晗; 黄 珊
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(天津医科大学基础医学院细胞生物学系,天津 300070)
- Author(s):
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YAN Han; HUANG Shan
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(Department of Cell Biology,School of Basic Medical Sciences,Tianjin Medical University,Tianjin 300070,China)
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- 关键词:
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姜黄素; 人结直肠癌SW-620细胞; 活性氧簇; 细胞凋亡; 细胞迁移
- Keywords:
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curcumin; human colorectal colon SW- -620 cells; intracellular reactive oxy gen species ; cell apoptosis; cell migration
- 分类号:
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R965.1
- DOI:
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10.20135/j.issn.1006-8147.2024.06.0479
- 文献标志码:
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A
- 摘要:
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目的:研究姜黄素(Cur)对人结直肠癌SW-620细胞生长、迁移的抑制作用。方法:不同浓度Cur(2、5、10 μg/mL)处理SW-620细胞后,采用MTT法检测细胞增殖能力变化,流式细胞仪分别结合Rh123、DCFH-DA、Annexin V-FITC/PI染色检测细胞线粒体膜电位(Δψm)变化、活性氧簇(ROS)生成及细胞凋亡情况,彗星电泳观察细胞DNA损伤情况,荧光显微技术观察细胞凋亡特征,Transwell实验检测细胞迁移能力,扫描电子显微镜观察细胞表面结构变化。结果:与对照组相比,5、10 μg/mL Cur处理24、48 h可显著抑制细胞增殖(t=5.28、21.8、18.19、33.19,均P<0.01),半数抑制浓度分别为6.46、3.75 μg/mL。药物处理4 h,与对照组相比,2、5、10 μg/mL Cur组细胞内ROS生成分别增加至15.8%、30.2%和45%(t=3.64、7.4、13.8,均P<0.05);Δψm下降的细胞比例分别为22.7%、38.5%和72.7%(t=7.7、11.32、45.26,均P<0.01);药物处理12、24 h,2、5、10 μg/mL Cur组凋亡细胞比例分别为6.6%(t=3.79,P=0.11)、32.6%、68.7%(t=21.3、64.39,均P<0.01)和16.9%(t=10.37,P<0.05)、47.2%、78.9%(t=23.46、19.8,均P<0.01); 药物处理12 h,2、5、10 μg/mL Cur组迁移细胞的数量分别减少至79.66% (t=7.14,P<0.05)、53.36%和39.45% (t=21.91、25.04,均P< 0.01)。结论:Cur可抑制人结直肠癌SW-620细胞增殖和迁移。
- Abstract:
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Objective:To study the inhibitory effect of curcumin (Cur) on the growth and migration of human colorectal cancer SW-620 cells. Methods:After SW-620 cells were treated with different concentrations of Cur (2,5,10 μg/mL),MTT assay was used to detect the changes in cell proliferation ability compared with the control group. The changes of mitochondrial membrane potential (Δψm),generation of reactive oxygen species (ROS) and apoptosis were detected by flow cytometry with Rh123,DCFH-DA and Annexin V-FITC/PI staining,respectively. Comet assay was used to detect DNA damage. Cell apoptosis was observed by fluorescence microscopy.Transwell assay was used to detect cell migration ability,and scanning electron microscopy was used to observe the changes of cell surface structure. Results:Compared with the control group,the proliferation of SW-620 cells was significantly inhibited by 5,10 μg/mL Cur for 24 and 48 h (t=5.28,21.8,18.19,33.19,all P<0.01),and the half maximal inhibitory concentrations were 6.46 and 3.75 μg/mL,respectively. 2,5,10 μg/mL Cur group induced intracellular ROS production increased to 15.8%,30.2% and 45% after 4 h of Cur treatment (t=3.64,7.4,13.8,all P<0.05),and the proportion of cells with Δψm decreased to 22.7%,38.5% and 72.7% (t=7.7,11.32,45.26,all P<0.01),respectively. The proportions of apoptotic cells after 12 and 24 h treatment in 2,5,10 μg/mL Cur group were 6.6% (t=3.79,P=0.11),32.6%,68.7% (t=21.3,64.39,both P<0.01) and 16.9% (t=10.37,P<0.05),47.2%,78.9% (t=23.46, 19.8,both P<0.01). The cell migration rate in 2,5,10 μg/mL Cur group were decreased to 79.66% (t=7.14,P<0.05),53.36% and 39.45% at 12 h,respectively (t=21.91,25.04,both P<0.05). Conclusion:Cur can inhibit the proliferation and migration of human colorectal cancer SW-620 cells.
参考文献/References:
[1] LU L,MULLINS C S,SCHAFMAYER C,et al. A global assessment of recent trends in gastrointestinal cancer and lifestyle-associated risk factors[J]. Cancer Commun (Lond),2021,41(11):1137-1151.
[2] SUNG H,FERLAY J,SIEGEL R L,et al. Global cancer statistics 2020:globocan estimates of incidence and mortality worldwide for 36 cancers in 185 countries[J]. CA Cancer J Clin,2021,7(3):209-249.
[3] XIA C,DONG X,LI H,et al. Cancer statistics in China and United States,2022:profiles,trends,and determinants[J]. Chin Med J (Engl),2022,135(5):584-590.
[4] CAO W,CHEN H D,YU Y W,et al. Changing profiles of cancer burden worldwide and in China:a secondary analysis of the global cancer statistics 2020[J]. Chin Med J (Engl),2021,134(7):783-791.
[5] DONG C,DING Y,WENG S,et al. Update in version 2021 of CSCO guidelines for colorectal cancer from version 2020[J]. Chin J Cancer Res,2021,33(3):302-307.
[6] UROSEVIC M,NIKOLIC L,GAJIC I,et al. Curcumin:biological activities and modern pharmaceutical forms[J]. Antibiotics (Basel),2022,11(2):135.
[7] GHADERI S,BABAEI E,HUSSEN B M,et al. Gemini curcumin suppresses proliferation of ovarian cancer ovcar-3 cells via induction of apoptosis[J]. Anticancer Agents Med Chem,2021,21(6):775-781.
[8] HE W,XIA Y,CAO P,et al. Curcuminoid WZ35 synergize with cisplatin by inducing ROS production and inhibiting TrxR1 activity in gastric cancer cells[J]. J Exp Clin Cancer Res,2019,38(1):207.
[9] LI M,GUO T,LIN J,et al. Curcumin inhibits the invasion and metastasis of triple negative breast cancer via Hedgehog/Gli1 signaling pathway[J]. J Ethnopharmacol,2022,283:114689.
[10] WOOD D A,ROBBINS G F,ZIPPIN C,et al. Staging of cancer of the colon and cancer of the rectum[J]. Cancer,1979,43(3):961-968.
[11] 张艳飞,刘莉,丁彦青. 具有相同遗传背景的人结肠癌细胞系生物学特性的鉴定[J]. 临床与实验病理学杂志,2008,24(1):86-90.
[12] LAM M,OLEINICK N L,NIEMINEN A L. Photodynamic therapy-induced apoptosis in epidermoid carcinoma cells. Reactive oxygen species and mitochondrial inner membrane permeabilization[J]. J Biol Chem,2001,276(50):47379-47386.
[13] KURT S,ALTAN SARIKAYA N. Correlation of self-efficacy and symptom control in cancer patients[J]. Support Care Cancer,2022, 30(7):5849-5857.
[14] BIAN Y,ZENG H,TAO H,et al. A pectin-like polysaccharide from Polygala tenuifolia inhibits pancreatic cancer cell growth in vitro and in vitro by inducing apoptosis and suppressing autophagy[J]. Int J Biol Macromol,2020,162:107-115.
[15] XU R,WU J,ZHANG X,et al. Modified Bu-zhong-yi-qi decoction synergies with 5 fluorouracile to inhibits gastric cancer progress via PD-1/PD- L1-dependent T cell immunization[J]. Pharmacol Res,2020,152:104623.
[16] YANG J,LI Y,CHAU C I,et al. Efficacy and safety of traditional Chinese medicine for cancer-related fatigue:a systematic literature review of randomized controlled trials[J]. Chin Med,2023,18(1):142.
[17] ZHANG Y M,MIAO Z M,CHEN Y P,et al. Ononin promotes radiosensitivity in lung cancer by inhibiting HIF-1alpha/VEGF pathway[J]. Phytomedicine,2024,125:155290.
[18] 贾福怀,王彩霞,袁媛,等. 姜黄保健食品开发现状分析[J]. 农产品加工,2020,19(7):69-72.
[19] 刘春艳. 姜黄的化学成分研究[D]. 沈阳医科大学,2008.
[20] OABEN T. Oxidative stress and apoptosis:impact on cancer therapy[J]. J Pharm Sci,2007,96(9):2181-2196.
[21] WISEMAN H,HALLIWELL B. Damage to DNA by reactive oxygen and nitrogen species:role in inflammatory disease and progression to cancer[J]. Biochem J,1996,313 ( Pt 1):17-29.
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备注/Memo
- 备注/Memo:
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基金项目 天津市自然科学基金青年项目(23JCQNJC01270)
作者简介 阎晗(1989-),女,助理实验师,硕士,研究方向:细胞生物学,E-mail:yanhan1989@tmu.edu.cn。
更新日期/Last Update:
2024-11-25