Isolation and characterization of tumorspheres from a recurrent pineoblastoma patient: Feasibility of a patient-derived xenograft

Jiyong Kwak, Jin Kyoung Shim, Dong Seok Kim, Ji Hyun Lee, Junjeong Choi, Junseong Park, Kyoung Jin Shin, Se Hoon Kim, Pilnam Kim, Yong Min Huh, Eui Hyun Kim, Jong Hee Chang, Sun Ho Kim, Seok Gu Kang

Research output: Contribution to journalArticlepeer-review

13 Citations (Scopus)

Abstract

The existence of tumorspheres (TSs) might confer treatment resistance to pineoblastoma (PB). The existence of PB TSs with cellular immortalization potential has not yet been reported. We developed a procedure for isolating TSs from recurrent PB (rPB) and tested whether their properties made them suitable for use as a patient-derived xenograft (PDX). Immunocytochemical staining, RT-PCR and quantitative real-time PCR showed that, among stemness proteins, CD133, musashi and podoplanin were expressed at elevated levels in rPB TSs, but nestin was not. rPB TSs cultured under neuro-glial differentiation conditions expressed TUBB3, but not GFAP, MBP or NeuN. Unlike glioblastoma TSs, rPB TSs showed no clear evidence of invasion in 3D invasion assay or increased expression of genes associated with epithelialmesenchymal transition. An orthotopic xenograft showed that tumor xenografts replicated the histopathological features of the patient tumor and expressed similar genome profiles, as determined by short tandem repeat genotyping. These data demonstrate the isolation and the characterization of rPB TSs for the first time. Using an orthotopic xenograft, we showed that rPB TSs could replicate the patient tumor, demonstrating their potential as a PDX for precision medicine.

Original languageEnglish
Pages (from-to)569-578
Number of pages10
JournalInternational journal of oncology
Volume49
Issue number2
DOIs
Publication statusPublished - 2016 Aug

Bibliographical note

Funding Information:
The present study was supported by a faculty research grant from the Yonsei University College of Medicine for 2013 (6-2013-0034), and by grants from the Basic Science Research Program through the National Research Foundation of Korea (NRF) funded by the Ministry of Education, Science and Technology (NRF-2013R1A1A2006427), and the Korean Health Technology R&D Project, Ministry of Health & Welfare, Republic of Korea (HI13C1509).

All Science Journal Classification (ASJC) codes

  • Oncology
  • Cancer Research

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