Subcellular progression of mesenchymal transition identified by two discrete synchronous cell lines derived from the same glioblastoma
- Authors
- Kim, Sojin; Park, Soo-Ji; Chowdhury, Tamrin; Hong, Jeong-Im; Ahn, Jinhee; Jeong, Tae Yeong; Yu, Hyeon Jong; Shin, Young-Kyoung; Ku, Ja-Lok; Park, Jong Bae; Hur, Junho K.; Lee, Hwajin; Kim, Kyoungmi; Park, Chul-Kee
- Issue Date
- 3월-2022
- Publisher
- SPRINGER BASEL AG
- Keywords
- Glioblastoma; Intratumoral heterogeneity; Mesenchymal transition; Synchronous cell lines
- Citation
- CELLULAR AND MOLECULAR LIFE SCIENCES, v.79, no.3
- Indexed
- SCIE
SCOPUS
- Journal Title
- CELLULAR AND MOLECULAR LIFE SCIENCES
- Volume
- 79
- Number
- 3
- URI
- https://scholar.korea.ac.kr/handle/2021.sw.korea/139355
- DOI
- 10.1007/s00018-022-04188-3
- ISSN
- 1420-682X
- Abstract
- Glioblastomas (GBM) exhibit intratumoral heterogeneity of various oncogenic evolutional processes. We have successfully isolated and established two distinct cancer cell lines with different morphological and biological characteristics that were derived from the same tissue sample of a GBM. When we compared their genomic and transcriptomic characteristics, each cell line harbored distinct mutation clusters while sharing core driver mutations. Transcriptomic analysis revealed that one cell line was undergoing a mesenchymal transition process, unlike the other cell line. Furthermore, we could identify four tumor samples containing our cell line-like clusters from the publicly available single-cell RNA-seq data, and in a set of paired longitudinal GBM samples, we could confirm three pairs where the recurrent sample was enriched in the genes specific to our cell line undergoing mesenchymal transition. The present study provides direct evidence and a valuable source for investigating the ongoing process of subcellular mesenchymal transition in GBM, which has prognostic and therapeutic implications.
- Files in This Item
- There are no files associated with this item.
- Appears in
Collections - Graduate School > Department of Biomedical Sciences > 1. Journal Articles
Items in ScholarWorks are protected by copyright, with all rights reserved, unless otherwise indicated.