Investigation of Cross-Contamination and Misidentification of 278 Widely Used Tumor Cell Lines

PLoS One. 2017 Jan 20;12(1):e0170384. doi: 10.1371/journal.pone.0170384. eCollection 2017.

Abstract

In recent years, biological research involving human cell lines has been rapidly developing in China. However, some of the cell lines are not authenticated before use. Therefore, misidentified and/or cross-contaminated cell lines are unfortunately commonplace. In this study, we present a comprehensive investigation of cross-contamination and misidentification for a panel of 278 cell lines from 28 institutes in China by using short tandem repeat profiling method. By comparing the DNA profiles with the cell bank databases of ATCC and DSMZ, a total of 46.0% (128/278) cases with cross-contamination/misidentification were uncovered coming from 22 institutes. Notably, 73.2% (52 out of 71) of the cell lines established by the Chinese researchers were misidentified and accounted for 40.6% of total misidentification (52/128). Further, 67.3% (35/52) of the misidentified cell lines established in laboratories of China were HeLa cells or a possible hybrid of HeLa with another kind of cell line. Furthermore, the bile duct cancer cell line HCCC-9810 and degenerative lung cancer Calu-6 exhibited 88.9% match in the ATCC database (9-loci), indicating that they were from the same origin. However, when we used 21-loci to compare these two cell lines with the same algorithm, the percent match was only 48.2%, indicating that these two cell lines were different. The SNP profiles of HCCC-9810 and Calu-6 also revealed that they were different cell lines. 150 cell lines with unique profiles demonstrated a wide range of in vitro phenotypes. This panel of 150 genomically validated cancer cell lines represents a valuable resource for the cancer research community and will advance our understanding of the disease by providing a standard reference for cell lines that can be used for biological as well as preclinical studies.

MeSH terms

  • Cell Line, Tumor
  • China
  • Genomic Instability
  • Humans
  • Neoplasms / pathology*

Grants and funding

This work was supported by the National Natural Sciences Foundation of China (No.31370185) and the National Basic Research Program of China (No. NSTI-CR14, NSTI-CR15). The funder's websites are [http://www.nsfc.gov.cn/publish/portal1/] and [http://www.most.gov.cn/eng/programmes1/200610/t20061009_36223.htm]. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.