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[Corrigendum] Antitumor effects of IDN5109 on head and neck squamous cell carcinoma
Daisuke Sano1, Hideki Matsuda1, Yukari Ishiguro1
1Department of Biology and Function in the Head and Neck, Yokohama City University Graduate School of Medicine, 3-9 Fukuura, Kanazawa-ku, Yokohama 236-0004, Japan.
Abstract:
Oncol Rep 15: [Related article:] 329–334, 2006; DOI: 10.3892/or.15.2.329 After the publication of the article, the authors noted that the relevance of the findings reported in this article on IDN5109 inhibition of growth of head and neck squamous cell carcinoma (HNSCC) is now in question. To examine the antitumor effect of IDN5109, this study was conducted using YCU-H891 and KCC-MS871 cell lines that the authors believed to be HNSCC cell lines. Because different human leukocyte antigen (HLA) was detected in 2 cell lines (KCC-TCM901 and KCC-T873) which were derived from the same patient in an experiment after publication, 16 cell lines established in our institution were analyzed by short tandem repeat (STR) analysis. STR analysis revealed that genotype of KCC-TCM901, YCU-H891 and KCC-MS871 was identical to that of HeLa cells, and that genotype of YCU-T891 was identical to that of YCU-L891, which was considered to be cross-contamination.
Insights
This study questions previous findings on IDN5109's effect on head and neck squamous cell carcinoma (HNSCC). Cell line analysis revealed contamination, with YCU-H891 and KCC-MS871 misidentified as HNSCC, impacting prior research conclusions.
Area of Science:
- Oncology
- Cell Biology
- Genetics
Background:
- Previous research investigated IDN5109's potential to inhibit head and neck squamous cell carcinoma (HNSCC) growth.
- Post-publication, concerns arose regarding the accuracy of cell lines used in the original study.
- Human leukocyte antigen (HLA) analysis indicated potential discrepancies in cell line origins.
Purpose of the Study:
- To re-evaluate the antitumor effects of IDN5109 on head and neck squamous cell carcinoma (HNSCC).
- To verify the identity and purity of cell lines, specifically YCU-H891 and KCC-MS871, previously used in HNSCC research.
- To address concerns about potential cross-contamination affecting experimental results.
Main Methods:
- Short tandem repeat (STR) analysis was performed on 16 established cell lines.
- Genotyping was conducted to compare cell lines against known standards, including HeLa.
- Human leukocyte antigen (HLA) typing was used to assess cell line origins.
Main Results:
- STR analysis revealed that YCU-H891, KCC-MS871, and KCC-TCM901 share an identical genotype with HeLa cells.
- The cell line YCU-T891 showed identical genotype to YCU-L891, suggesting cross-contamination.
- These findings indicate that the cell lines used were not authentic HNSCC cell lines as initially believed.
Conclusions:
- The relevance of the original study's findings on IDN5109 inhibition of HNSCC growth is now uncertain due to cell line misidentification.
- The study highlights the critical importance of rigorous cell line authentication in cancer research.
- Future studies investigating IDN5109 or HNSCC should utilize properly validated cell lines to ensure reliable results.
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