bioRxivCancer BiologyPreprint
Depletion of FH, an essential TCA cycle enzyme, drives proliferation in a two-step model
B. Solaimuthu, M. Lichtenstein, A. Hayashi, A. Khatib, I. Plaschkes, Y. Nevo, M. Tanna, S. Lavi, O. Pines, Y. D. Shaul
Abstract
Several tumor suppressor genes do not follow the canonical function of cell cycle repressors. For example, fumarate hydratase (FH) is an evolutionary conserved TCA cycle enzyme that reversibly catalyzes the hydration of fumarate to L-malate and has a moonlight function in the DNA damage response (DDR). Interestingly, despite this enzymes essential role in central carbon metabolism, FH is inactive or absent in several tumors, such as hereditary leiomyomatosis and renal cell cancer (HLRCC). Accordingly, FH has a contradictory cellular function, as it is pro-survival through its role in the TCA cycle, yet its loss can drive tumorigenesis. These observations have supported the role of FH as a tumor suppressor. Here, we solved this contradiction by determining the molecular mechanisms that allow the cells to survive and even proliferate upon FH loss. We found that the cells response to FH loss is separated into two distinct time frames based on cell proliferation and DNA damage repair. During the early stages of FH loss, the cells proliferation and DNA damage repair are inhibited. However, over time the cells overcome the FH loss and form knockout clones, indistinguishable from WT cells in their proliferation rate. Due to the FH loss effect on DNA damage repair, we assumed that the recovered cells bear adaptive mutations. Therefore, we applied whole-exome sequencing to identify such mutated genes systematically. Indeed, we identified recurring mutations in genes belonging to the central oncogenic signaling pathways, such as JAK/STAT, which we validated to be impaired in FH-KO clones. Intriguingly, we demonstrated that these adaptive mutations are responsible for FH-KO cell proliferation under TCA cycle malfunction.
- organism: human
- assay: whole-exome sequencing
- research focus: variant calling
- approach: statistical model
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- HIRA loss transforms FH-deficient cells
L. Valcarcel-Jimenez, C. Rogerson, … C. Frezza·bioRxiv·Jun 4, 2022
- FH variant pathogenicity promotes purine salvage pathway dependence in kidney cancer
B. R. Wilde, N. Chakraborty, … H. R. Christofk·bioRxiv·Aug 15, 2022
- The Landscape of Mutations in Fumarate Hydratase
D. Shorthouse, M. W. J. Hall, B. A. Hall·bioRxiv·Jan 31, 2020
- Heterogeneous adaptation of cysteine reactivity to a covalent oncometabolite
M. Perez, D. W. Bak, … J. L. Meier·bioRxiv·Jun 25, 2020
- FOXA2 controls the anti-oxidant response in FH-deficient cells
C. Rogerson, M. Sciacovelli, … C. Frezza·bioRxiv·Jul 4, 2022
- Oncometabolite fumarate impairs ATR-CHK1 signaling by succinating RPA1 in Fumarate Hydratase-deficient renal cell carcinoma cells
Nian Liu, Changxian Shen, … Binghui Shen·Cancer & MetabolismPeer-reviewed·Apr 28, 2026