PT  - JOURNAL ARTICLE
AU  - Ella N Perrault
AU  - Jack M Shireman
AU  - Eunus S Ali
AU  - Isabelle Preddy
AU  - Peiyu Lin
AU  - Cheol Park
AU  - Luke Tomes
AU  - Andrew J Zolp
AU  - Shreya Budhiraja
AU  - Shivani Baisiwala
AU  - C. David James
AU  - Issam Ben-Sahra
AU  - Sebastian Pott
AU  - Anindita Basu
AU  - Atique U Ahmed
TI  - Ribonucleotide Reductase Regulatory Subunit M2 as a Driver of Glioblastoma TMZ-Resistance through Modulation of dNTP Production
AID  - 10.1101/2021.11.23.469785
DP  - 2021 Jan 01
TA  - bioRxiv
PG  - 2021.11.23.469785
4099  - http://biorxiv.org/content/early/2021/11/24/2021.11.23.469785.short
4100  - http://biorxiv.org/content/early/2021/11/24/2021.11.23.469785.full
AB  - Glioblastoma (GBM) remains one of the most resistant and fatal forms of cancer. Previous studies have examined primary and recurrent GBM tumors, but it is difficult to study tumor evolution during therapy where resistance develops. To investigate this, we performed an in vivo single-cell RNA sequencing screen in a patient-derived xenograft (PDX) model. Primary GBM was modeled by mice treated with DMSO control, recurrent GBM was modeled by mice treated with temozolomide (TMZ), and during therapy GBM was modeled by mice euthanized after two of five TMZ treatments. Our analysis revealed the cellular population present during therapy to be distinct from primary and recurrent GBM. We found the Ribonucleotide Reductase gene family to exhibit a unique signature in our data due to an observed subunit switch to favor RRM2 during therapy. GBM cells were shown to rely on RRM2 during therapy causing RRM2-knockdown (KD) cells to be TMZ-sensitive. Using targeted metabolomics, we found RRM2-KDs to produce less dGTP and dCTP than control cells in response to TMZ (p<0.0001). Supplementing RRM2-KDs with deoxycytidine and deoxyguanosine rescued TMZ-sensitivity, suggesting an RRM2-driven mechanism of chemoresistance, established by regulating the production of these nucleotides. In vivo, tumor-bearing mice treated with the RRM2-inhibitor, Triapine, in combination with TMZ, survived longer than mice treated with TMZ alone (p<0.01), indicating promising clinical opportunities in targeting RRM2. Our data present a novel understanding of RRM2 activity, and its alteration during therapeutic stress as response to TMZ-induced DNA damage.Competing Interest StatementThe authors have declared no competing interest.