Search bioRxiv⌕ Search

Biology subjects

Watters, V.

Publications and source records attributed to Watters, V..

2 recordsLinked to original sources

Establishment of human glioblastoma cell culture collection

Glioblastoma (GBM) is a highly aggressive primary brain cancer with poor prognosis (<15 months), highlighting the urgent need for more effective therapies. As current treatments are not effective, the need for a deeper understanding of the biology of GBM cells, including how they reprogram their metabolism to support their aberrant and uncontrolled growth, is critical. To this end, we established a collection of 41 human glioma cell lines derived from freshly resected tumour tissues from 99 patients. We characterized 12 of these cell lines by combining histologic, genetic, stem cell derivation and self-renewal, and metabolomic analyses. Histological and genetic profiles included IDH mutation status, Ki-67 proliferation index, ATRX status, mutant TP53 expression, chromosome 10q loss, EGFR amplification, and MGMT promoter methylation. Of these, only p53 mutation expression status showed weak segregation of the cell lines into 2 separate metabolic groups based on amino acid levels, but none showed an effect on stem cell derivation or self-renewal. Further characterization of these 12 cell lines revealed significant metabolic and phenotypic differences when comparing mesenchymal versus proneural gene expression subtyping. We show significant increases in TCA cycle metabolites in mesenchymal-like GBM cells and higher overall metabolic activity compared to proneural-like cells. These findings highlight the complexity of GBM and the need for personalized treatments that consider the metabolome of each subtype as a potential therapeutic avenue.

cancer biology↗

Long-read RNA sequencing identifies isoform switching of a novel long non-coding RNA that promotes somatic cell reprogramming

Development of long-read RNA sequencing technologies has paved the way to the exploration of RNA isoform diversity and its relevance in regulating cell fate. However, identifying new functional isoforms is still very difficult. Here, we leverage long-read RNA sequencing to study changes in isoforms during somatic cell reprogramming and identify novel isoforms occurring throughout cell state transitions. We demonstrate tight regulation of non-coding isoforms and show that isoform switching plays previously overlooked functional roles and outcomes in gene regulation and cell fate changes. We uncover a novel long non-coding RNA, Snhg26, that undergoes isoform switching during reprogramming to enhance the conversion of differentiated cells towards the pluripotent state. Knock-down of Snhg26 in mouse and human pluripotency models reveals that it is important for pluripotency acquisition. Together, our study provides a resource to study full-length isoform usage during cell fate change. It also demonstrates the power of long-read sequencing to identify functionally relevant gene isoforms in the context of cell plasticity.

cell biology↗