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PMID: 9009106 Published · ppublish English Comparative Study Journal Article

Assessment of the invasive potential of human gynecological tumor cell lines with the in vitro Boyden chamber assay: influences of the ability of cells to migrate through the filter membrane.

Clinical & experimental metastasis ·Vol. 15 ·No. 1 ·1997-01-00 ·Pages 53-62

Sieuwerts AM, Klijn JG, Foekens JA

Abstract

The Boyden chamber assay is widely used for in vitro measurement of the invasive capacity of cells. However, results can be affected significantly if certain precautions are not taken. Using the Boyden chamber assay we investigated in vitro the invasive potential of a variety of human gynecological tumor cell lines to degrade and migrate through the artificial basement membrane matrix Matrigel. However, in the absence of this Matrigel layer large differences were observed in the ability of cells to adhere to, migrate through and attach to the lower side of the filter membranes. These differences were influenced by cell density, degree of directional locomotion, and the size of the filter pores. To adjust for these influences (which are not directly correlated to the capacity of cells to traverse the Matrigel layer), invasion results were corrected for the ability of cells to migrate through the filter membrane. In addition, the invasion of MDA-MB-231 cells was used as an internal standard to compensate for variations in the Matrigel layer between different experiments. Overall, in our experimental set up, the five human breast cancer cell lines were the most invasive (mean invasion +/- SEM relative to MDA-MB-231 invasion: 104.7 +/- 6.1%), the five human ovarian cancer cell lines the least invasive (60.2 +/- 2.2%) and the six human endometrial cancer cell lines showed an intermediate capacity (79.1 +/- 3.5%). In conclusion, the Boyden chamber assay can be used reliably for studying the invasive potential of cells in vitro, if the ability of the cells to migrate through the filter is taken into account, and a reference cell line is included to enable comparison of the data obtained from independently performed experiments on different cell lines.

MeSH Terms
3T3 Cells/metabolism Animals Breast Neoplasms/pathology Cell Count Cell Culture Techniques/instrumentation Cell Movement Cell Size Collagen/metabolism,pharmacology Culture Media, Conditioned/pharmacology Drug Combinations Endometrial Neoplasms/pathology Female Fibronectins/metabolism,pharmacology Filtration/instrumentation Genital Neoplasms, Female/pathology Humans Laminin/metabolism,pharmacology Membranes, Artificial Mice Neoplasm Invasiveness Ovarian Neoplasms/pathology Polycarboxylate Cement Proteoglycans/metabolism,pharmacology Tumor Cells, Cultured
Chemicals
Culture Media, Conditioned Drug Combinations Fibronectins Laminin Membranes, Artificial Polycarboxylate Cement Proteoglycans matrigel polycarbonate Collagen
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Sieuwerts A M
Department of Medical Oncology, Rotterdam Cancer Institute (Daniel den Hoed Kliniek) / Academic Hospital, The Netherlands. Sieuwerts@bidh.azr.nl
Klijn J G
Foekens J A
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Article Info
Journal
Clinical & experimental metastasis
Abbr.
Clin Exp Metastasis
ISSN
0262-0898
Published
1997-01-00
Pages
53-62
Language
English
Region
Netherlands
NLM ID
8409970
Subset
IM
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