4.7 Article

Epitope detection in monocytes (EDIM) for liquid biopsy including identification of GD2 in childhood neuroblastoma-a pilot study

Journal

BRITISH JOURNAL OF CANCER
Volume 127, Issue 7, Pages 1324-1331

Publisher

SPRINGERNATURE
DOI: 10.1038/s41416-022-01855-x

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Funding

  1. BD Bioscience, Heidelberg, Germany
  2. Open Access Publishing Fund of Tuebingen University
  3. Madeleine Schickedanz Kinderkrebsstiftung, Furth, Germany
  4. Projekt DEAL
  5. Zyagnum AG, Pfungstadt, Germany

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This study analyzed the role of epitope detection in monocytes (EDIM) technique for liquid biopsy in neuroblastoma (NB) patients. The results showed that the EDIM test could serve as a non-invasive tool for liquid biopsy in pediatric NB patients, aiding in risk stratification, tumor biology research, treatment monitoring, and early detection of tumor relapses.
Background Neuroblastoma (NB) is the most common paediatric extracranial solid malignancy. We analysed the role of the epitope detection in monocytes (EDIM) technique for liquid biopsy in NB patients. Methods Tumour epitopes transketolase-like 1 (TKTL1), Apo10 (DNaseX) and GD2 were assessed: expression levels in seven NB tumour samples and five NB cell lines were analysed using RT-PCR and flow cytometry. LAN-1 cells were co-cultured with blood and assessed using EDIM. Peripheral blood macrophages of patients with neuroblastoma (n = 38) and healthy individuals (control group, n = 37) were labelled (CD14(+)/CD16(+)) and assessed for TKTL1, Apo10 and GD2 using the EDIM technology. Results mRNA expression of TKTL1 and DNaseX/Apo10 was elevated in 6/7 NB samples. Spike experiments showed upregulation of TKTL1, Apo10 and GD2 in LAN-1 cells following co-culturing with blood. TKTL1 and Apo10 were present in macrophages of 36/38 patients, and GD2 in 15/19 patients. The 37 control samples were all negative. EDIM expression scores of the three epitopes allowed differentiation between NB patients and healthy individuals. Conclusions The EDIM test might serve as a non-invasive tool for liquid biopsy in children suffering from NB. Future studies are necessary for assessing risk stratification, tumour biology, treatment monitoring, and early detection of tumour relapses.

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