False and mycoplasma-contaminated leukemia-lymphoma cell lines: time for a reappraisal

Int J Cancer. 2017 Mar 1;140(5):1209-1214. doi: 10.1002/ijc.30530.

Abstract

Leukemia-lymphoma cell lines are important research tools in a variety of fields. To represent adequate model systems it is of utmost importance that cell lines faithfully model the primary tumor material and are not cross-contaminated with unrelated cell material (or contaminated with mycoplasma). As it has been previously reported that cross-contaminated cell lines represent a significant problem, it is of interest to know whether any improvement in the prevalence of such "false cell lines" had occurred since we called the alert in 1999. A retrospective review of our data archives covered 848 cell lines received from 1990 to 2014 from 290 laboratories in 23 countries spanning the spectrum of leukemia-lymphoma entities. Two variables were considered: authenticity and freedom from mycoplasma infection. Regarding provenance, we separately considered primary sources (original investigators having established the cell lines or reference repositories) and secondary sources. The percentages of mycoplasma-contaminated cell lines decreased significantly over the 25-year timespan. Among primary sourced material: mycoplasma-contamination fell from 23% to 0%; among secondary sourced: from 48% to 21%. The corresponding figures for cross-contamination declined from 15% to 6%, while among material obtained from secondary sources prevalence remained remarkably high, throughout the time periods at 14-18%. Taken together, our data indicate that using non-authenticated cell lines from secondary sources carries a risk of about 1:6 for obtaining a false cell line. The use of authentic leukemia-lymphoma cell lines holds important translational value for their model character and the reproducibility of the laboratory data in the clinical arena.

Keywords: authentification; cell lines; leukemia; lymphoma; mycoplasma.

MeSH terms

  • Cell Line, Tumor / microbiology*
  • DNA Fingerprinting
  • Humans
  • In Situ Hybridization
  • Karyotyping
  • Leukemia / pathology*
  • Lymphoma / pathology*
  • Mycoplasma / isolation & purification*
  • Retrospective Studies