切换至 "中华医学电子期刊资源库"

中华妇幼临床医学杂志(电子版) ›› 2015, Vol. 11 ›› Issue (01) : 14 -17. doi: 10.3877/cma.j.issn.1673-5250.2015.01.004

所属专题: 文献

论著

叶黄素对人宫颈癌HeLa细胞增殖和凋亡的影响
刘会芳1, 赵元华1, 何荣霞1,*,*(), 王芳1   
  1. 1. 730030 兰州大学第二医院妇产科
  • 收稿日期:2014-08-09 修回日期:2014-12-29 出版日期:2015-02-01
  • 通信作者: 何荣霞

Effects of lutein on cell proliferation and apoptosis of human cervical cancer HeLa cells

Huifang Liu1, Yuanhua Zhao1, Rongxia He1(), Fang Wang1   

  1. 1. Department of Gynaecology and Obstetrics, Lanzhou University Second Hospital, Lanzhou 730000, Gansu Province, China
  • Received:2014-08-09 Revised:2014-12-29 Published:2015-02-01
  • Corresponding author: Rongxia He
  • About author:
    Corresponding author: He Rongxia, Email:
引用本文:

刘会芳, 赵元华, 何荣霞, 王芳. 叶黄素对人宫颈癌HeLa细胞增殖和凋亡的影响[J]. 中华妇幼临床医学杂志(电子版), 2015, 11(01): 14-17.

Huifang Liu, Yuanhua Zhao, Rongxia He, Fang Wang. Effects of lutein on cell proliferation and apoptosis of human cervical cancer HeLa cells[J]. Chinese Journal of Obstetrics & Gynecology and Pediatrics(Electronic Edition), 2015, 11(01): 14-17.

目的

探讨叶黄素对体外培养的人宫颈癌HeLa细胞增殖和凋亡的影响。

方法

选择对数生长期的人宫颈癌HeLa细胞为研究对象,采用随机数字表法,将其随机分为6组:20,40,80,160,320 μmol/L叶黄素组及对照组,叶黄素组分别加入200 μL含20,40,80,160,320 μmol/L叶黄素终浓度的RPMI1640培养基及HeLa细胞,对照组仅加入200 μL RPMI1640培养基及HeLa细胞。采用噻唑蓝(MTT)法检测人宫颈癌HeLa细胞增殖抑制率,并采用流式细胞术检测HeLa细胞凋亡率。采用统计学方法分析相同时间不同浓度叶黄素培养及相同浓度叶黄素培养不同时间的HeLa细胞增殖抑制率及凋亡率差异。

结果

HeLa细胞在培养时间相同(为24 h或48 h或72 h)时,随着叶黄素浓度依次增加(分别为20,40,80,160,320 μmol/L)均较前一低浓度组的增殖抑制率及凋亡率显著升高,且差异均有统计学意义(P<0.01);HeLa细胞在叶黄素浓度相同(为20 μmol/L或40 μmol/L或80 μmol/L或160 μmol/L或320 μmol/L)培养时,随着培养时间增加(分别为24,48,72 h)均较前一时间点的增殖抑制率及凋亡率显著升高,且差异有统计学意义(P<0.01)。

结论

叶黄素可抑制体外培养的人宫颈癌HeLa细胞的增殖,诱导其凋亡,并且HeLa细胞体外培养的增殖抑制率及凋亡率分别随着叶黄素浓度增加及作用时间延长而升高。

Objective

To observe the effects of lutein on cell proliferation and apoptosis of in vitro culture human cervical cancer HeLa cells.

Methods

Select human HeLa cells of the logarithmic growth phase for the study. Using a random number table method, those HeLa cells were randomly divided into six groups: 20, 40, 80, 160, 320 μmol/L lutein group and control group, then added 200 μL RPMI1640 medium contained final concentration of 20, 40, 80, 160, 320 μmol/L lutein and HeLa cells in 20, 40, 80, 160, 320 μmol/L lutein group, respectively, and added 200 μL RPMI1640 medium only and HeLa cells in control group.The HeLa cells proliferation inhibitory rates were determined by methyl thiazolyl tetrazolium(MTT) assay and the apoptosis rates of HeLa cells were determined by flow cytometry.Analyzed rates of proliferation inhibitory and apoptosis of HeLa cells that cultured the same time but in different concentrations of lutein and cultured in the same concentration of lutein but at different time points by statistical method.

Results

When HeLa cells cultured the same time(24 h or 48 h or 72 h), with lutein concentration increased by turns(20, 40, 80, 160, 320 μmol/L, respectively), compared with the previous low concentration group, the proliferation inhibitory rates and apoptosis rates increased significantly, and the differences were statistically significant(P<0.01); When HeLa cells cultured in the same concentration(20 μmol/L or 40 μmol/L or 80 μmol/L or 160 μmol/L or 320 μmol/L) of lutein, with the culture time extended (24, 48, 72 h, respectively), compared with the previous time point, the proliferation inhibitory rates and apoptosis rates were significantly increased, and the differences were statistically significant(P<0.01).

Conclusions

Lutein can inhibit the cell proliferation and induce the apoptosis of in vitro culture human HeLa cells.The rates of proliferation inhibitory and apoptosis of in vitro culture human HeLa cells could increase with lutein concentration increasing and culture time prolonging.

表1 相同时间不同浓度叶黄素培养及相同浓度叶黄素培养不同时间HeLa细胞增殖抑制率比较(%,±s)
Table 1 Comparison of proliferation inhibitory rates of HeLa cells cultured within the same time but in different concentrations of lutein,and cultured in the same concentration of lutein but at different time points(%,±s)
表2 相同时间不同浓度叶黄素培养及相同浓度叶黄素培养不同时间HeLa细胞凋亡率比较(%,±s)
Table 2 Comparison of apoptosis rates of HeLa cells cultured within the same time but in different concentrations of lutein,and cultured in the same concentration of lutein but at different time points(%, ±s)
[1]
Mignone LI, Giovannucci E, Newcomb PA,et al. Dietary carotenoids and the risk of invasive breast cancer[J]. Int J Cancer,2009,124(12): 2929–2937.
[2]
冀波.Lutein对胃癌SGC-7901细胞的作用及分子机制研究[D].郑州:郑州大学,2012.
[3]
李莉,任广伟,赵昱,等.叶黄素对体外培养的人食管癌Ec-9706细胞增殖和凋亡的影响[J].河北医科大学学报,2013,34(3):249–252.
[4]
孙震,奚海燕,李博,等.叶黄素和玉米黄素抑制口腔上皮细胞癌增殖的实验研究[J].食品科学,2006,27(6):207–211.
[5]
Moss SF,Blaser MJ. Mechanisms of disease:inflammation and the origins of cancer[J].Nat Clin Pract Oncol,2005,2(2):90–97.
[6]
Bartsch H, Nair J. Chronic inflammation and oxidative stress in the genesis and perpetuation of cancer: role of lipid peroxidation,DNA damage,and repair[J]. Langenbecks Arch Surg,2006,391(5):499–510.
[7]
Tamimi RM,Colditz GA,Hankinson SE.Circulating carotenoids,mammographic density,and subsequent risk of breast cancer[J]. Cancer Res,2009,69(24): 9323–9329.
[8]
Wang L,Li B,Pan MX,et al. Specific carotenoid intake is inversely associated with the risk of breast cancer among Chinese women[J]. Br J Nutr,2014,111(9): 1686–1695.
[9]
Lakshminarayana R,Aruna G,Sathisha UV,et al. Structural elucidation of possible lutein oxidation products mediated through peroxyl radical inducer 2, 2'-Azobis (2-methylpropionamidine) dihydrochloride:antioxidant and cytotoxic influence of oxidized lutein in HeLa cells[J]. Chem boil interact,2013,203(2): 448–455.
[10]
朱金林,许新德,孙晓霞,等.叶黄素咀嚼片毒理学安全性评价[J].中国食品添加剂,2012, (4):158–165.
[11]
Guo ZY,Hao XH,Tan FF,et al.The elements of human cyclin D1 promoter and regulation involved[J].Clin Epigenetics,2011,2(2):63–76.
[12]
黄雪坤,尚慧玲,张四友,等.原花青素对宫颈癌HeLa细胞Caspase-3和Survivin基因表达的影响[J/CD].中华妇幼临床医学杂志:电子版,2011,7(3):222–226.
[13]
Cho H,Kim MK,Lee JK,et al. Relationship of serum antioxidant micronutrients and sociodemographic factors to cervical neoplasia:a case-control study[J]. Clin Chem Lab Med,2009,47(8):1005–1012.
[14]
Tong SY, Lee JM,Song ES,et al. Functional polymorphism in manganese superoxide dismutase and antioxidant status:their interactions on the risk of cervical intraepithelial neoplasia and cervical cancer[J].Gynecol Oncol,2009,115(2): 272–276.
[1] 孔莹莹, 谢璐涛, 卢晓驰, 徐杰丰, 周光居, 张茂. 丁酸钠对猪心脏骤停复苏后心脑损伤的保护作用及机制研究[J]. 中华危重症医学杂志(电子版), 2023, 16(05): 355-362.
[2] 张晓燕, 肖东琼, 高沪, 陈琳, 唐发娟, 李熙鸿. 转录因子12过表达对脓毒症相关性脑病大鼠大脑皮质的保护作用及其机制[J]. 中华妇幼临床医学杂志(电子版), 2023, 19(05): 540-549.
[3] 周伟, 蔡恒, 范海迪, 李惠中, 王传霞, 顾茂胜. cblC型甲基丙二酸血症MMACHC基因新突变对小鼠神经细胞凋亡及Wnt/β-catenin信号通路的作用机制[J]. 中华妇幼临床医学杂志(电子版), 2022, 18(05): 528-539.
[4] 孙佳辰, 宋垚垚, 申传安, 赵虹晴, 孙天骏. 表皮和表皮干细胞衰老的研究进展[J]. 中华损伤与修复杂志(电子版), 2022, 17(06): 531-534.
[5] 江振剑, 蒋明, 黄大莉. TK1、Ki67蛋白在分化型甲状腺癌组织中的表达及预后价值研究[J]. 中华普外科手术学杂志(电子版), 2023, 17(06): 623-626.
[6] 刘硕儒, 王功炜, 张斌, 李书豪, 胡成. 新型溶瘤病毒M1激活内质网应激致前列腺癌细胞凋亡的机制[J]. 中华腔镜泌尿外科杂志(电子版), 2023, 17(04): 388-393.
[7] 邓春文, 陈嵩, 钟裴, 闵师强, 万健. LncRNA CRNDE通过miR-181a-5p/SOX6轴调节脂多糖诱导人肺泡上皮细胞的炎症反应和细胞凋亡[J]. 中华细胞与干细胞杂志(电子版), 2023, 13(03): 129-136.
[8] 刘燕, 叶亚萍, 郑艳莉. 干扰LINC00466通过miR-493-3p/MIF抑制子宫内膜癌RL95-2细胞恶性生物学行为[J]. 中华细胞与干细胞杂志(电子版), 2023, 13(03): 151-158.
[9] 田鹏飞, 王丽娟, 肖圣超. 黄芪总黄酮通过调控miR-190a-5p对缺氧/复氧诱导的心肌细胞损伤的影响[J]. 中华细胞与干细胞杂志(电子版), 2022, 12(06): 346-352.
[10] 莫钊鸿, 翟航, 苏日顺, 孟泓宇, 罗豪, 陈文豪, 许瑞云. U2AF2表达对肝细胞癌增殖和迁移的影响及其与预后的关系[J]. 中华肝脏外科手术学电子杂志, 2023, 12(03): 336-341.
[11] 魏志鸿, 郭娟, 江哲龙, 江艺, 吕立志. miR-4458靶向结合BZW2对肝癌细胞增殖、迁移和侵袭的影响[J]. 中华肝脏外科手术学电子杂志, 2023, 12(01): 108-113.
[12] 张师垚, 徐岩岩, 张琦, 李春强, 赵智成, 刘刚. m6A结合蛋白YTHDC2调节p38MAPK信号通路影响结直肠癌细胞凋亡[J]. 中华结直肠疾病电子杂志, 2023, 12(02): 117-124.
[13] 于迪, 于海波, 吴焕成, 李玉明, 苏彬, 陈馨. 发状分裂相关增强子1差异表达对胆固醇刺激下血管内皮细胞的影响[J]. 中华脑科疾病与康复杂志(电子版), 2023, 13(05): 264-270.
[14] 张懿炜, 胡亚欣, 出良钊, 严昭, 曾茜, 蒲茜. CREB3通过下调FAK磷酸化水平抑制胶质瘤细胞增殖及侵袭转移的体外实验研究[J]. 中华临床医师杂志(电子版), 2023, 17(02): 202-209.
[15] 邱甜, 杨苗娟, 胡波, 郭毅, 何奕涛. 亚低温治疗脑梗死机制的研究进展[J]. 中华脑血管病杂志(电子版), 2023, 17(05): 518-521.
阅读次数
全文


摘要