Development of Multicellular Tumor Spheroid (MCTS) Culture from Breast Cancer Cell and a High Throughput Screening Method Using the MTT Assay

被引:139
作者
Ho, Wan Yong [1 ]
Yeap, Swee Keong [2 ]
Ho, Chai Ling [1 ]
Rahim, Raha Abdul [1 ]
Alitheen, Noorjahan Banu [1 ]
机构
[1] Univ Putra Malaysia, Fac Biotechnol & Biomol Sci, Dept Cell & Mol Biol, Serdang, Selangor, Malaysia
[2] Univ Putra Malaysia, Inst Biosci, Serdang, Selangor, Malaysia
关键词
IN-VITRO; MODEL; GENERATION; INHIBITOR; APOPTOSIS; EVALUATE; THERAPY; GROWTH;
D O I
10.1371/journal.pone.0044640
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
摘要
In comparison to monolayer cells, MCTS has been claimed as more suitable candidate for studying drug penetration due to the high resemblance to solid tumors. However, the cultivation of MCTS is cumbersome, time consuming, and most technique fail to generate spheroids with uniform sizes. Therefore, the application of spheroid cultures in high throughput screening has been rather limiting. Besides, the lack of a well established screening protocol method that is applicable to spheroid could also be attributed to this limitation. Here we report a simple way of cultivating homogenous MCTS cultures with compact and rigid structure from the MCF-7 cells. Besides, we had also made some modifications to the standard MTT assay to realize high throughput screening of these spheroids. Using the modified protocol, tamoxifen showed cytotoxicity effect towards MCTS cultures from MCF-7 with high consistency. The results correlated well with the cultures' response assessed by LDH release assay but the latter assay was not ideal for detecting a wide range of cytotoxicity due to high basal background reading. The MTT assay emerged as a better indicator to apoptosis event in comparison to the LDH release assay. Therefore, the method for spheroid generation and the modified MTT assay we reported here could be potentially applied to high throughput screening for response of spheroid cultures generated from MCF-7 as well as other cancer cell lines towards cytotoxic stimuli.
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页数:7
相关论文
共 25 条
[1]
Baron M, 2012, ECOTOXICOLOGY, P1
[2]
Braidy N, 2009, INT J TRYPTOPHAN RES, V2, P61
[3]
Complement activation by necrotic cells in normal plasma environment compares to that by late apoptotic cells and involves predominantly IgM [J].
Ciurana, CLF ;
Zwart, B ;
van Mierlo, G ;
Hack, CE .
EUROPEAN JOURNAL OF IMMUNOLOGY, 2004, 34 (09) :2609-2619
[4]
Multicellular tumor spheroid model to evaluate spatio-temporal dynamics effect of chemotherapeutics: application to the gemcitabine/CHK1 inhibitor combination in pancreatic cancer [J].
Dufau, Isabelle ;
Frongia, Celine ;
Sicard, Flavie ;
Dedieu, Laure ;
Cordelier, Pierre ;
Ausseil, Frederic ;
Ducommun, Bernard ;
Valette, Annie .
BMC CANCER, 2012, 12
[5]
Effect of therapeutic macromolecules in spheroids [J].
Fracasso, G ;
Colombatti, M .
CRITICAL REVIEWS IN ONCOLOGY HEMATOLOGY, 2000, 36 (2-3) :159-178
[6]
Screening for compounds that induce apoptosis of cancer cells grown as multicellular spheroids [J].
Herrmann, Richard ;
Fayad, Walid ;
Schwarz, Stephan ;
Berndtsson, Maria ;
Linder, Stig .
JOURNAL OF BIOMOLECULAR SCREENING, 2008, 13 (01) :1-8
[7]
Ho WY, 2011, J MED PLANTS RES, V5, P5741
[8]
The phosphatidylinositol 3-kinase inhibitor, PX-866, is a potent inhibitor of cancer cell motility and growth in three-dimensional cultures [J].
Howes, Amy L. ;
Chiang, Gary G. ;
Lang, Elizabeth S. ;
Ho, Caroline B. ;
Powis, Garth ;
Vuori, Kristiina ;
Abraham, Robert T. .
MOLECULAR CANCER THERAPEUTICS, 2007, 6 (09) :2505-2514
[9]
Rapid generation of single-tumor spheroids for high-throughput cell function and toxicity analysis [J].
Ivascu, Andrea ;
Kubbies, Manfred .
JOURNAL OF BIOMOLECULAR SCREENING, 2006, 11 (08) :922-932
[10]
Jin C, 2010, BIOMEDICINE PHARMACO