Advanced Search

Journal Navigation

Journal Home

Subscriptions

Archive

Contact Us

Table of Contents

Sign In to gain access to subscriptions and/or personal tools.
Journal of Biomolecular Screening
This Article
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
1087057106292763v1
11/8/922    most recent
Right arrow References
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to Saved Citations
Right arrow Download to citation manager
Right arrowRequest Permissions
Right arrow Request Reprints
Right arrow Add to My Marked Citations
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Web of Science (6)
Right arrow Citing Articles via Google Scholar
Right arrow Citing Articles via Scopus
Google Scholar
Right arrow Articles by Ivascu, A.
Right arrow Articles by Kubbies, M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Ivascu, A.
Right arrow Articles by Kubbies, M.
Social Bookmarking
 Add to CiteULike   Add to Complore   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Reddit   Add to Technorati   Add to Twitter  
What's this?

Rapid Generation of Single-Tumor Spheroids for High-Throughput Cell Function and Toxicity Analysis

Andrea Ivascu

Roche Pharmaceutical Research Oncology, Penzberg, Germany

Manfred Kubbies

Roche Pharmaceutical Research Oncology, Penzberg, Germany

Spheroids are widely used in biology because they provide an in vitro 3-dimensional (3D) model to study proliferation, cell death, differentiation, and metabolism of cells in tumors and the response of tumors to radiotherapy and chemotherapy. The methods of generating spheroids are limited by size heterogeneity, long cultivation time, or mechanical accessibility for higher throughput fashion. The authors present a rapid method to generate single spheroids in suspension culture in individual wells. A defined number of cells ranging from 1000 to 20,000 were seeded into wells of poly-HEMA-coated, 96-well, round-or conical-bottom plates in standard medium and centrifuged for 10 min at 1000g. This procedure generates single spheroids in each well within a 24-h culture time with homogeneous sizes, morphologies, and stratification of proliferating cells in the rim and dying cells in the core region. Because a large number of tumor cell lines form only loose aggregates when cultured in 3D, the authors also performed a screen for medium additives to achieve a switch from aggregate to spheroid morphology. Small quantities of the basement membrane extract Matrigel, added to the culture medium prior to centrifugation, most effectively induced compact spheroid formation. The compact spheroid morphology is evident as early as 24 h after centrifugation in a true suspension culture. Twenty tumor cell lines of different lineages have been used to successfully generate compact, single spheroids with homogenous size in 96-well plates and are easily accessible for subsequent functional analysis.

Key Words: tumor • spheroid • cell aggregate • Matrigel (rBM) • apoptosis • high-throughput screening

This version was published on December 1, 2006

Journal of Biomolecular Screening, Vol. 11, No. 8, 922-932 (2006)
DOI: 10.1177/1087057106292763


Add to CiteULike CiteULike   Add to Complore Complore   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati   Add to Twitter Twitter    What's this?


This article has been cited by other articles:


Home page
Sci SignalHome page
B. Schoeberl, E. A. Pace, J. B. Fitzgerald, B. D. Harms, L. Xu, L. Nie, B. Linggi, A. Kalra, V. Paragas, R. Bukhalid, et al.
Therapeutically Targeting ErbB3: A Key Node in Ligand-Induced Activation of the ErbB Receptor-PI3K Axis
Sci. Signal., June 30, 2009; 2(77): ra31 - ra31.
[Abstract] [Full Text] [PDF]


Home page
Cancer Res.Home page
S. Singer, M. Malz, E. Herpel, A. Warth, M. Bissinger, M. Keith, T. Muley, M. Meister, H. Hoffmann, R. Penzel, et al.
Coordinated Expression of Stathmin Family Members by Far Upstream Sequence Element-Binding Protein-1 Increases Motility in Non-Small Cell Lung Cancer
Cancer Res., March 15, 2009; 69(6): 2234 - 2243.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
D. Barbone, T.-M. Yang, J. R. Morgan, G. Gaudino, and V. C. Broaddus
Mammalian Target of Rapamycin Contributes to the Acquired Apoptotic Resistance of Human Mesothelioma Multicellular Spheroids
J. Biol. Chem., May 9, 2008; 283(19): 13021 - 13030.
[Abstract] [Full Text] [PDF]


Home page
J Biomol ScreenHome page
R. Herrmann, W. Fayad, S. Schwarz, M. Berndtsson, and S. Linder
Screening for Compounds That Induce Apoptosis of Cancer Cells Grown as Multicellular Spheroids
J Biomol Screen, January 1, 2008; 13(1): 1 - 8.
[Abstract] [PDF]


Home page
FASEB J.Home page
D. M. Dean, A. P. Napolitano, J. Youssef, and J. R. Morgan
Rods, tori, and honeycombs: the directed self-assembly of microtissues with prescribed microscale geometries
FASEB J, December 1, 2007; 21(14): 4005 - 4012.
[Abstract] [Full Text] [PDF]