|本期目录/Table of Contents|

[1]吴潇然.乳腺癌基质成纤维细胞分离培养的优化及对乳腺癌细胞作用的初步研究[J].天津医科大学学报,2017,23(06):489-492.
 WU Xiao-ran.Optimization of isolation and culture of breast cancer stromal fibroblasts and their effects on breast cancer cells MDA-MB-231 and MCF7[J].Journal of Tianjin Medical University,2017,23(06):489-492.
点击复制

乳腺癌基质成纤维细胞分离培养的优化及对乳腺癌细胞作用的初步研究(PDF)
分享到:

《天津医科大学学报》[ISSN:1006-8147/CN:12-1259/R]

卷:
23卷
期数:
2017年06期
页码:
489-492
栏目:
基础医学
出版日期:
2017-11-20

文章信息/Info

Title:
Optimization of isolation and culture of breast cancer stromal fibroblasts and their effects on breast cancer cells MDA-MB-231 and MCF7
文章编号:
1006-8147(2017)06-0480-04
作者:

吴潇然

(天津医科大学肿瘤医院肿瘤研究所,国家肿瘤临床医学研究中心,天津市“肿瘤防治”重点实验室,乳腺癌防治教育部重点实验室,天津 300060)

Author(s):
WU Xiao-ran
(Cancer Institute and Hospital, Tianjin Medical University, National Clinical Research Center of Cancer, Tianjin Key Laboratory of Cancer Prevention and Therapy, Key Laboratory of Breast Cancer Prevention and Therany, Tianjin Medical University, Ministry of Education, Tianjin 300060,China)
关键词:
乳腺癌癌相关成纤维细胞分离原代培养转移
Keywords:
breast cancer cancer-associated fibroblasts isolation primary culture metastasis
分类号:
R737.9
DOI:
-
文献标志码:
A
摘要:
目的: 分离培养乳腺癌基质成纤维细胞,初步探讨其生物学特性及对乳腺癌细胞增殖转移能力的影响。方法: 取自临床手术新鲜标本,用Ⅰ型胶原酶和透明质酸酶消化法获得原代乳腺癌成纤维细胞(CAFs)及与之配对的正常乳腺成纤维细胞(NFs);显微镜观察细胞形态;免疫印迹和免疫荧光实验检测上皮细胞、间质细胞和成纤维细胞标志物表达;胶原收缩实验比较细胞收缩能力;平板克隆形成和Transwell细胞体外迁移侵袭实验,观测CAFs和NFs对乳腺癌细胞增殖、迁移和侵袭能力的影响。结果: 分离得到CAFs和NFs,2次传代后可获得纯化细胞;成纤维细胞中高表达Vimentin和α-SMA,低表达E-cadherin;CAFs胶原收缩能力较NFs更强;CAFs条件培养基处理后的乳腺癌细胞体外增殖、迁移和侵袭能力增强。结论:成功获得CAFs和NFs,且与NFs相比,CAFs活化程度更高,CAFs对乳腺癌细胞体外增殖和转移能力的促进作用更强。
Abstract:
Objective: To isolate and culture primary breast cancer stroma fibroblasts, to explore their biological characteristics, and also to study their influence on proliferation and metastasis of breast cancer cells. Methods: The primary breast cancer tissues were obtained from fresh specimen. Primary breast cancer associated fibroblasts(CAFs)and their paired normal breast fibroblasts(NFs)were isolated by collagenase and hyaluronidase digestion. Morphology was observed by microscope. Cell markers were detected by western blot and immunofluorescence. The collagen gel contraction assay was used to compare the contractile ability of CAFs and NFs. The influence of CAFs and NFs on proliferation and metastasis of breast cancer cells was measured by colony formation assay and transwell assay. Results: The purified CAFs and NFs were maintained after passage 2. The protein levels of Vimentin and α-SMA were highly expressed, however, the protein level of E-cadherin was not detected in CAFs and NFs. The contractile ability of CAFs was stronger than NFs. CAFs-CM could promote the ability of proliferation, migration and invasion of breast cancer cells compared with NFs-CM. Conclusion: The isolation and primary culture of CAFs and NFs with digestion method could be performed successfully. The status of activation of CAFs and the ability of CAFs to promote proliferation and metastasis of breast cancer cells are higher than NFs.

参考文献/References:

[1]Mao Y, Keller E T, Garfield D H, et al. Stromal cells in tumor microenvironment and breast cancer[J].Cancer Metastasis Rev, 2013,32(1/2):303
[2]Swartz M A, Iida N, Roberts E W, et al. Tumor microenvironment complexity: emerging roles in cancer therapy[J].Cancer Res,2012,72(10):2473
[3]Fleming J M, Miller T C, Quinones M, et al. The normal breast microenvironment of premenopausal women differentially influences the behavior of breast cancer cells in vitro and in vivo[J].BMC Med,2010,8:27
[4]Cichon M A, Degnim A C, Visscher D W, et al. Microenvironmental influences that drive progression from benign breast disease to invasive breast cancer[J].J Mammary Gland Biol Neoplasia,2010,15(4):389
[5]Saito R A, Micke P, Paulsson J, et al. Forkhead box F1 regulates tumor-promoting properties of cancer-associated fibroblasts in lung cancer[J].Cancer Res,2010,70(7):2644
[6]Joyce J A. Therapeutic targeting of the tumor microenvironment[J]. Cancer Cell,2005,7(6):513
[7]Franco O E, Shaw A K, Strand D W, et al. Cancer associated fibroblasts in cancer pathogenesis[J].Semin Cell Dev Biol,2010,21(1):33
[8]Erez N, Truitt M, Olson P, et al. Cancer-Associated fibroblasts are activated in incipient neoplasia to orchestrate Tumor-Promoting inflammation in an NF-kappaB-Dependent manner[J].Cancer Cell, 2010,17(2):135
[9]Allaoui R, Bergenfelz C, Mohlin S, et al. Cancer-associated fibroblast-secreted CXCL16 attracts monocytes to promote stroma activation in triple-negative breast cancers[J].Nat Commun, 2016,7:13050
[10]Ko S Y, Barengo N, Ladanyi A, et al. HOXA9 promotes ovarian cancer growth by stimulating cancer-associated fibroblasts[J].J Clin Invest,2012,122(10):3603
[11]Rupp C, Scherzer M, Rudisch A, et al. IGFBP7, a novel tumor stroma marker, with growth-promoting effects in colon cancer through a paracrine tumor-stroma interaction[J].Oncogene,2015,34(7):815
[12]Micke P, Ostman A. Tumour-stroma interaction: cancer-associated fibroblasts as novel targets in anti-cancer therapy?[J].Lung Cancer,2004,45(Suppl 2):S163
[13]Underwood T J, Hayden A L, Derouet M, et al. Cancer-associated fibroblasts predict poor outcome and promote periostin-dependent invasion in oesophageal adenocarcinoma[J].J Pathol,2015,235(3):466
[14]Heldin C H, Rubin K, Pietras K, et al. High interstitial fluid pressure - an obstacle in cancer therapy[J].Nat Rev Cancer,2004,4(10):
806
[15]Neri S, Hashimoto H, Kii H, et al. Cancer cell invasion driven by extracellular matrix remodeling is dependent on the properties of cancer-associated fibroblasts[J].J Cancer Res Clin Oncol, 2016, 142(2):437
[16]Gascard P, Tlsty T D. Carcinoma-associated fibroblasts: orchestrating the composition of malignancy[J].Genes Dev, 2016, 30(9):1002

相似文献/References:

[1]朱悦,张诗武,张丹芳,等.TA2小鼠自发乳腺癌血清蛋白质组学研究[J].天津医科大学学报,2013,19(05):373.
[2]刘 营,孙保存,刘铁菊,等.AURKA蛋白激酶在三阴乳腺癌干细胞形成血管拟态中的实验研究[J].天津医科大学学报,2013,19(06):437.
 LIU Ying,SUN Bao-cun,LIU Tie-ju,et al.Experimental study of AURKA protein kinase in the formation of vascular mimicry in triple-negative breast cancer stem cells[J].Journal of Tianjin Medical University,2013,19(06):437.
[3]伦淑敏.HOXA5基因真核表达质粒的构建及在乳腺癌细胞中的功能研究[J].天津医科大学学报,2014,20(05):337.
 LUN Shu-min. Construction of HOXA5 eukaryotic expression plasmid of and its biological significance in breast cancer cells[J].Journal of Tianjin Medical University,2014,20(06):337.
[4]伦淑敏.肌细胞增强因子2A基因真核表达质粒的构建及对乳腺癌细胞MCF-7增殖能力的影响[J].天津医科大学学报,2014,20(06):429.
 LUN Shu-min.Construction of myocyte enhancer factor 2A eukaryotic expression plasmid and effects on cell proliferation in breast cancer cell line MCF7[J].Journal of Tianjin Medical University,2014,20(06):429.
[5]孙秀梅,张 飞,田 然,等.Nanog表达上调促进乳腺癌细胞MCF-7的增殖和侵袭[J].天津医科大学学报,2014,20(06):421.
 SUN Xiu-mei,ZHANG Fei,TIAN Ran,et al.Up-regulation of Nanog promotes cell proliferation and invasion in breast cancer cells MCF-7[J].Journal of Tianjin Medical University,2014,20(06):421.
[6]张 洁,张 飞,冀 为,等. SHP2不同突变体对乳腺癌细胞的迁移和侵袭能力的影响[J].天津医科大学学报,2015,21(02):93.
 ZHANG Jie,ZHANG Fei,JI Wei,et al. Effect of different SHP2 mutants on breast cancer cell migration and invasion[J].Journal of Tianjin Medical University,2015,21(06):93.
[7]蔡 隽. FOXQ1稳定表达乳腺癌细胞系的建立及鉴定[J].天津医科大学学报,2015,21(04):292.
 CAI Jun.Establishment and identification of cell lines with stable expression of FOXQ1 in MDA-MB-231-luc[J].Journal of Tianjin Medical University,2015,21(06):292.
[8]蔡 隽 综述,冯玉梅 审校.叉头框转录因子调控乳腺癌生物学特性的研究进展[J].天津医科大学学报,2015,21(05):455.
[9]任宗娜.沉默Notch4基因对乳腺癌细胞系MDA-MB-231增殖和迁移侵袭能力的影响[J].天津医科大学学报,2015,21(06):469.
 REN Zong-na.Inhibition effect of?silencing?? Notch4 gene on the proliferation and migration and invasion activity of? breast cancer cell line?MDA-MB-231[J].Journal of Tianjin Medical University,2015,21(06):469.
[10]周岩,宋伟杰,张飞,等.人附睾蛋白4在乳腺癌发生发展中的机制研究[J].天津医科大学学报,2015,21(06):466.
 ZHOU Yan,SONG Wei-jie,ZHANG Fei,et al.Mechanism of human epididymis protein 4 in development and progression of breast cancer[J].Journal of Tianjin Medical University,2015,21(06):466.

备注/Memo

备注/Memo:
作者简介 吴潇然(1991-),女,硕士在读,研究方向:乳腺癌微环境中成纤维细胞活化机制, E-mail:wxrwxr151@163.com
更新日期/Last Update: 2017-11-14