Original paper
Cell density dependent plating efficiency affects outcome and interpretation of colony forming assays

https://doi.org/10.1016/0167-8140(96)01767-7Get rights and content

Abstract

Background and purpose. The usefulness of colony forming assays (CFA) has been established for almost 40 years (Puck and Marcus, J. Exp. Med. 103: 653–666,1956). Although time-consuming and not successful for all cell lines, it is generally considered to be the gold standard of assays for testing the sensitivity of cell lines to ionizing radiation or other cytotoxic agents in vitro. We recently found for several cell lines that the plating efficiencies of both control and irradiated cells is dependent upon the density of cells seeded for colony formation; that is, increasing cell inoculum levels resulted in a non-linear relationship with colony formation, even at relatively low colony numbers. Material and methods. All data from a human melanoma cell line, transfected with c-myc or N-ras, as well as from normal human diploid fibroblasts, were taken to see how this phenomenon influenced outcome and interpretation of clonogenic assays. Survival was recalculated using all data, or only data with a linear relationship between inoculum level and colony formation. Results. It is found that when data with a non-linear relationship between inoculum level and colony formation are included, survival can be underestimated due to inhibition of colony formation in treated cultures. Conclusion. For validity, colony forming assays must be standardized to assure a constant relationship between the cell density and colony forming efficiency. This usually requires a much lower density of colonies than has been typically published for many cell survival studies.

References (9)

  • F.B. Geara et al.

    Radiosensitivity measurement of keratinocytes and fibro-blasts from radiotherapy patients

    Int. J. Radiat. Oncol. Biol. Phys.

    (1992)
  • C. Aubert et al.

    Tumorigenicity of human malignant melanocytes in nude mice in relation to their differentiation in vitro

    J. Natl. Cancer Inst.

    (1980)
  • J.F. Eliason et al.

    Non-linearity of colony formation by human tumour cells from biopsy samples

    Br. J. Cancer

    (1985)
  • F.B. Geara et al.

    Intrinsic radiosensitivity of normal human fibroblasts and lymphocytesafter high- and low-dose-rate irradiation

    Cancer Res.

    (1992)
There are more references available in the full text version of this article.

Cited by (36)

  • Hydroxyethyl disulfide as an efficient metabolic assay for cell viability in vitro

    2012, Toxicology in Vitro
    Citation Excerpt :

    Although one or many of these approaches have been used for more than three decades in biomedical sciences, each one of them has disadvantages ranging from non-linearity to high background and complicated cumbersome and time consuming protocols. Clonogenic assay is a measure of colony (50 cells/colony) forming ability of a single cell, which quantifies the cytotoxic effects of drugs or radiation (Franken et al., 2006; Kuwahara et al., 2010; Pomp et al., 1996; Wouters et al., 2010). Most studies for high throughput screening (HTS) of cancer drugs avoid using this assay because of the difficulties in terms of time consuming and complicated protocols combined with low plating efficiency (PE) of the cells at low density (Pomp et al., 1996).

View all citing articles on Scopus
View full text