Engineering a High-Throughput 3-D In Vitro Glioblastoma Model

Glioblastoma multiforme (GBM) is the most common and malignant primary brain tumor in adults because of its highly invasive behavior. The existing treatment for GBM, which involves a combination of resection, chemotherapy, and radiotherapy, has a very limited success rate with a median survival rate of <;1 year. This is mainly because of the failure of early detection and effective treatment. We designed a novel 3-D GBM cell culture model based on microwells that could mimic in vitro environment and help to bypass the lack of suitable animal models for preclinical toxicity tests. Microwells were fabricated from simple and inexpensive polyethylene glycol material for the control of in vitro 3-D culture. We applied the 3-D micropatterning system to GBM (U-87) cells using the photolithography technique to control the cell spheroids' shape, size, and thickness. Our preliminary results suggested that uniform GBM spheroids can be formed in 3-D, and the size of these GBM spheroids depends on the size of microwells. The viability of the spheroids generated in this manner was quantitatively evaluated using live/dead assay and shown to improve over 21 days. We believe that in vitro 3-D cell culture model could help to reduce the time of the preclinical brain tumor growth studies. The proposed novel platform could be useful and cost-effective for high-throughput screening of cancer drugs and assessment of treatment responses.

[1]  Chu Zhang,et al.  Hyaluronic acid-based hydrogels as 3D matrices for in vitro evaluation of chemotherapeutic drugs using poorly adherent prostate cancer cells. , 2009, Biomaterials.

[2]  A. Brandes,et al.  State-of-the-art treatment of high-grade brain tumors. , 2003, Seminars in oncology.

[3]  K. Aldape,et al.  Anti-vascular endothelial growth factor therapy-induced glioma invasion is associated with accumulation of Tie2-expressing monocytes , 2014, Oncotarget.

[4]  Ivan Martin,et al.  Three‐dimensional culture of melanoma cells profoundly affects gene expression profile: A high density oligonucleotide array study , 2005, Journal of cellular physiology.

[5]  Kenneth M. Yamada,et al.  Taking Cell-Matrix Adhesions to the Third Dimension , 2001, Science.

[6]  H. Avraham,et al.  VEGF165 requires extracellular matrix components to induce mitogenic effects and migratory response in breast cancer cells , 2001, Oncogene.

[7]  R. Wheelhouse,et al.  Glioblastoma Multiforme Therapy and Mechanisms of Resistance , 2013, Pharmaceuticals.

[8]  Kristi S Anseth,et al.  Hydrogels in Healthcare: From Static to Dynamic Material Microenvironments. , 2013, Acta materialia.

[9]  S. Sahoo,et al.  3-D tumor model for in vitro evaluation of anticancer drugs. , 2008, Molecular pharmaceutics.

[10]  L. Parada,et al.  Malignant Glioma: Lessons from Genomics, Mouse Models, and Stem Cells , 2012, Cell.

[11]  Maria Vinci,et al.  Advances in establishment and analysis of three-dimensional tumor spheroid-based functional assays for target validation and drug evaluation , 2012, BMC Biology.

[12]  M. Guiou,et al.  Novel Therapies in Glioblastoma , 2012, Neurology research international.

[13]  Rashid Bashir,et al.  Three-dimensional photopatterning of hydrogels using stereolithography for long-term cell encapsulation. , 2010, Lab on a chip.

[14]  E. Lengyel,et al.  Use of a novel 3D culture model to elucidate the role of mesothelial cells, fibroblasts and extra‐cellular matrices on adhesion and invasion of ovarian cancer cells to the omentum , 2007, International journal of cancer.

[15]  C. Ries,et al.  Comparison of 3D and 2D tumor models reveals enhanced HER2 activation in 3D associated with an increased response to trastuzumab , 2009, Oncogene.

[16]  H. Avraham,et al.  VEGF(165) requires extracellular matrix components to induce mitogenic effects and migratory response in breast cancer cells. , 2001, Oncogene.

[17]  Jayanta Debnath,et al.  The Role of Apoptosis in Creating and Maintaining Luminal Space within Normal and Oncogene-Expressing Mammary Acini , 2002, Cell.

[18]  Tayyaba Hasan,et al.  Three-dimensional ovarian cancer models: imaging and therapeutic combinations , 2010, BiOS.

[19]  D. Hanahan,et al.  The Hallmarks of Cancer , 2000, Cell.

[20]  R. Kerbel,et al.  Multicellular gastric cancer spheroids recapitulate growth pattern and differentiation phenotype of human gastric carcinomas. , 2001, Gastroenterology.

[21]  Tobias Schmelzle,et al.  Engineering tumors with 3D scaffolds , 2007, Nature Methods.

[22]  A. Maier,et al.  Clonogenic assay with established human tumour xenografts: correlation of in vitro to in vivo activity as a basis for anticancer drug discovery. , 2004, European journal of cancer.

[23]  R. Sutherland Cell and environment interactions in tumor microregions: the multicell spheroid model. , 1988, Science.

[24]  Jayanta Debnath,et al.  Modelling glandular epithelial cancers in three-dimensional cultures , 2005, Nature Reviews Cancer.

[25]  Ali Khademhosseini,et al.  Directed assembly of cell-laden microgels for building porous three-dimensional tissue constructs. , 2011, Journal of biomedical materials research. Part A.

[26]  Adrian L. Harris,et al.  Hypoxia — a key regulatory factor in tumour growth , 2002, Nature Reviews Cancer.

[27]  Robert Langer,et al.  Micromolding of photocrosslinkable hyaluronic acid for cell encapsulation and entrapment. , 2006, Journal of biomedical materials research. Part A.

[28]  Kenneth M. Yamada,et al.  Modeling Tissue Morphogenesis and Cancer in 3D , 2007, Cell.

[29]  John W Haycock,et al.  3D cell culture: a review of current approaches and techniques. , 2011, Methods in molecular biology.

[30]  K. Beningo,et al.  Responses of fibroblasts to anchorage of dorsal extracellular matrix receptors , 2004, Proceedings of the National Academy of Sciences of the United States of America.

[31]  Anne-Marie Mes-Masson,et al.  Molecular description of a 3D in vitro model for the study of epithelial ovarian cancer (EOC) , 2007, Molecular carcinogenesis.

[32]  S. Grossman,et al.  Current management of glioblastoma multiforme. , 2004, Seminars in oncology.

[33]  G. Bernier,et al.  Brain Cancer Stem Cells: Current Status on Glioblastoma Multiforme , 2011, Cancers.

[34]  L. Deangelis,et al.  Chemotherapy for brain tumors--a new beginning. , 2005, The New England journal of medicine.

[35]  D P Byar,et al.  Randomized comparisons of radiotherapy and nitrosoureas for the treatment of malignant glioma after surgery. , 1980, The New England journal of medicine.

[36]  A. Khademhosseini,et al.  Hydrogels in Biology and Medicine: From Molecular Principles to Bionanotechnology , 2006 .

[37]  Jennifer L. West,et al.  Three‐Dimensional Biochemical and Biomechanical Patterning of Hydrogels for Guiding Cell Behavior , 2006 .

[38]  Jingxuan Yang,et al.  Deregulated Signaling Pathways in Glioblastoma Multiforme: Molecular Mechanisms and Therapeutic Targets , 2012, Cancer investigation.

[39]  C. Haslinger,et al.  Modeling colon adenocarcinomas in vitro a 3D co-culture system induces cancer-relevant pathways upon tumor cell and stromal fibroblast interaction. , 2011, The American journal of pathology.

[40]  Kinam Park,et al.  Development of an in vitro 3D tumor model to study therapeutic efficiency of an anticancer drug. , 2013, Molecular pharmaceutics.

[41]  K. Shah,et al.  Brain cancer stem cells , 2009, Journal of Molecular Medicine.

[42]  L. Kunz-Schughart,et al.  Multicellular tumor spheroids: an underestimated tool is catching up again. , 2010, Journal of biotechnology.

[43]  S. Pun,et al.  3-D tissue culture systems for the evaluation and optimization of nanoparticle-based drug carriers. , 2008, Bioconjugate chemistry.

[44]  L. Kunz-Schughart,et al.  Multicellular tumor spheroids: intermediates between monolayer culture and in vivo tumor , 1999, Cell biology international.

[45]  Santosh Kesari,et al.  Malignant gliomas in adults. , 2008, The New England journal of medicine.