[1]林 艳,林 倩,刘婷莉,等.重组IL-12对人乳腺癌细胞自噬的研究[J].医学信息,2019,32(23):64-69.[doi:10.3969/j.issn.1006-1959.2019.23.018]
　LIN Yan,LIN Qian,LIU Ting-li,et al.Study on Autophagy of Human Breast Cancer Cells by Recombinant IL-12[J].Medical Information,2019,32(23):64-69.[doi:10.3969/j.issn.1006-1959.2019.23.018]
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重组IL-12对人乳腺癌细胞自噬的研究()
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医学信息[ISSN:1006-1959/CN:61-1278/R]

卷:
32卷
期数:
2019年23期
页码:
64-69
栏目:
论著
出版日期:
2019-12-01

文章信息/Info

Title:
Study on Autophagy of Human Breast Cancer Cells by Recombinant IL-12
文章编号:
1006-1959（2019）23-0064-06
作者:
林 艳; 林 倩; 刘婷莉; 马玉华; 何春容; 梁树梅; 周明莉
（成都市第三人民医院临床医学检验部，四川 成都 610031）
Author(s):
LIN Yan; LIN Qian; LIU Ting-li; MA Yu-hua; HE Chun-rong; LIANG Shu-mei; ZHOU Ming-li
(Department of Clinical Medical Laboratory,Chengdu Third People’s Hospital,Chengdu 610031,Sichuan,China)
关键词:
自噬; 乳腺肿瘤; 重组人IL-12; PI3K/Akt通路
Keywords:
Autophagy; Breast tumor; Recombinant human IL-12; PI3K/ Akt pathway
分类号:
R737.9
DOI:
10.3969/j.issn.1006-1959.2019.23.018
文献标志码:
A
摘要:
目的 探讨重组人IL-12（rIL-12）对乳腺癌细胞自噬的影响。方法 两株乳腺癌细胞（MDA-MB-231和MCF7）分别用rIL-12处理，经免疫蛋白印迹技术和细胞免疫荧光技术检测其自噬微管相关蛋白轻链3（LC3）的变化，以观察自噬情况；另外，用透射电镜观察rIL-12处理乳腺癌细胞前后自噬小体的变化。分别用胰岛素样生长因子1（IGF-1）激活磷脂酰肌醇-3激酶/蛋白激酶B（PI3K/Akt）通路，再加入rIL-12处理后，蛋白免疫印迹法检测相关通路蛋白PI3K/Akt, 哺乳动物雷帕霉素靶点（TOR）磷酸化变化及LC3的表达。结果 与空白组相比，rIL-12组细胞的自噬标志蛋白LC3表达增高，差异有统计学意义（P＜0.05），且增加程度呈时间和浓度依赖性；荧光显微镜观察自噬体形成的结果显示，与空白组相比，rIL-12处理组的细胞核周点状聚集的绿色荧光增多；使用电镜观察到rIL-12处理组明显有自噬小体形成。与rIL-12组相比，IGF-1+rIL-12组的LC3Ⅱ表达减少，差异有统计学意义（P＜0.05）。结论 rIL-12可以激活乳腺癌细胞自噬，并通过抑制PI3K/Akt信号通路的机制，促进自噬标志蛋白LC3，特别是LC3Ⅱ的表达。
Abstract:
Objective To investigate the effect of recombinant human IL-12 (rIL-12) on breast cancer cell autophagy. Methods Two breast cancer cells (MDA-MB-231 and MCF7) were treated with rIL-12, and the changes of autophagy microtubule-associated protein light chain 3 (LC3) were detected by immunoblotting and cell immunofluorescence. Observe autophagy; in addition, observe the change of autophagosomes in breast cancer cells before and after treatment with rIL-12 using transmission electron microscopy. Insulin-like growth factor 1 (IGF-1) was used to activate the phosphatidylinositol-3 kinase / protein kinase B (PI3K / Akt) pathway, and then treated with rIL-12. Western blot was used to detect the related pathway protein PI3K / Akt , Mammalian rapamycin target (TOR) phosphorylation changes and LC3 expression. Results Compared with the blank group, the expression of autophagy marker protein LC3 in the cells of the rIL-12 group was significantly increased, the difference was statistically significant (P<0.05), and the degree of increase was time- and concentration-dependent; The results showed that, compared with the blank group, the green fluorescence around the nucleus in the rIL-12 treated group was significantly increased; it was observed that the autophagic bodies were formed in the rIL-12 treated group. Compared with rIL-12 group, the expression of LC3Ⅱ in IGF-1 + rIL-12 group was significantly reduced,the difference was statistically significant (P<0.05). Conclusion rIL-12 can activate the autophagy of breast cancer cells, and promote the expression of autophagy marker protein LC3, especially LC3Ⅱ through the mechanism of inhibiting PI3K / Akt signaling pathway.

参考文献/References:

[1]Furmaniak AC,Menig M,Markes MH.Exercise for women receiving adjuvant therapy for breast cancer[J].Cochrane Database Syst Rev,2016,2016(9):CD005001.[2]Jemal A,Bray F,Center MM,et al.Global cancer statistics[J].CA Cancer J Clin,2011,61(2):69-90.[3]Arroyo DS,Gaviglio EA,Peralta Ramos JM,et al.Autophagy in inflammation,infection, neurodegeneration and cancer[J].Int Immunopharmacol,2014,18(1):55-65.[4]Chen N,Karantza V.Autophagy as a therapeutic target in cancer[J].Cancer Biol Ther,2011,11(2):157-168. [5]Viry E,Paggetti J,Baginska J.Autophagy:an adaptive metabolic response to stress shaping the antitumor immunity[J].Biochem Pharmacol,2014,92(1):31-42.[6]Jiang P,Mizushima N.LC3-and p62-based biochemical methods for the analysis of autophagy progression in mammalian cells[J].Methods,2015,75:13-18.[7]Palumbo S,Pirtoli L,Tini P,et al.Different involvement of autophagy in human malignant glioma cell lines undergoing irradiation and temozolomide combined treatments[J].J Cell Biochem,2012,113(7):2308-2318.[8]Sun T,Li X,Zhang P.Acetylation of Beclin 1 inhibits autophagosome maturation and promotes tumour growth[J].Nat Commun,2015(6):7215.[9]Flynn AB,Schiemann WP.Autophagy in breast cancer metastatic dormancy:Tumor suppressing or tumor promoting functions[J].J Cancer Metastasis Treat,2019(5):43.[10]Correa RJM,Valdes YR,Shepherd TG,et al.Beclin-1 expression is retained in high-grade serous ovarian cancer yet is not essential for autophagy induction in vitro[J].J Ovarian Res,2015(8):52. [11]Bhat P,Kriel J,Shubha Priya B,et al.Modulating autophagy in cancer therapy:Advancements and challenges for cancer cell death sensitization[J].Biochem Pharmacol,2018(147):170-182.[12]Xu M,Mizoguchi I,Morishima N,et al.Regulation of antitumor immune responses by the IL-12 family cytokines,IL-12,IL-23,and IL-27[J].Clin Dev Immunol,2010,pii:832454. [13]Sangro B,Melero I,Qian C,et al.Gene therapy of cancer based on interleukin 12[J].Curr Gene Ther,2005(5):573-581.[14]Engel MA,Neurath MF.Anticancer properties of the IL-12 family-focus on colorectal cancer[J]. Curr Med Chem,2010,17(29):3303-3308. [15]Ma TT,Wu BT,Lin Y,et al.IL-12 could induce monocytic tumor cells directional differentiation[J].Mol Cell Biochem,2015(402):157-169. [16]Yla-Anttila P,Vihinen H,Jokitalo E,et al.Monitoring autophagy by electron microscopy in Mammalian cells[J].Methods Enzymol,2009(452):143-164.[17]Zhang J,Zhao D,Xie Z,et al.Down-regulation of AKT combined with radiation-induced autophagy and apoptosis roles in MCF-7 cells[J].Biomed Mater Eng,2015(Suppl 1):S2259-S2265. [18]Zhang J,Yu XH,Yan YG,et al.PI3K/Akt signaling in osteosarcoma[J].Clin Chim Acta,2015(444):182-192.[19]Vigneswaran N,Wu J,Song A,et al.Hypoxia-induced autophagic response is associated with aggressive phenotype and elevated incidence of metastasis in orthotopic immunocompetent murine models of head and neck squamous cell carcinomas(HNSCC)[J].Exp Mol Pathol,2011,90(2):215-225.

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更新日期/Last Update: 2019-12-01