Details

Autor(en) / Beteiligte

• Kanakkanthara, Arun
• Kurmi, Kiran
• Ekstrom, Thomas L
• Hou, Xiaonan
• Purfeerst, Emma R
• Heinzen, Ethan P
• Correia, Cristina
• Huntoon, Catherine J
• O'Brien, Daniel
• Wahner Hendrickson, Andrea E
• Dowdy, Sean C
• Li, Hu
• Oberg, Ann L
• Hitosugi, Taro
• Kaufmann, Scott H
• Weroha, S John
• Karnitz, Larry M

Titel

BRCA1 Deficiency Upregulates NNMT, Which Reprograms Metabolism and Sensitizes Ovarian Cancer Cells to Mitochondrial Metabolic Targeting Agents

Ist Teil von

• Cancer research (Chicago, Ill.), 2019-12, Vol.79 (23), p.5920-5929

Ort / Verlag

United States

Erscheinungsjahr

2019

Link zum Volltext

Quelle

MEDLINE

Beschreibungen/Notizen

• BRCA1 plays a key role in homologous recombination (HR) DNA repair. Accordingly, changes that downregulate BRCA1, including mutations and reduced transcription, due to promoter hypermethylation or loss of the BRCA1 transcriptional regulator CDK12, disrupt HR in multiple cancers. In addition, BRCA1 has also been implicated in the regulation of metabolism. Here, we show that reducing BRCA1 expression, either by CDK12 or BRCA1 depletion, led to metabolic reprogramming of ovarian cancer cells, causing decreased mitochondrial respiration and reduced ATP levels. BRCA1 depletion drove this reprogramming by upregulating nicotinamide N-methyltransferase (NNMT). Notably, the metabolic alterations caused by BRCA1 depletion and NNMT upregulation sensitized ovarian cancer cells to agents that inhibit mitochondrial metabolism (VLX600 and tigecycline) and to agents that inhibit glucose import (WZB117). These observations suggest that inhibition of energy metabolism may be a potential strategy to selectively target BRCA1-deficient high-grade serous ovarian cancer, which is characterized by frequent BRCA1 loss and NNMT overexpression. SIGNIFICANCE: Loss of BRCA1 reprograms metabolism, creating a therapeutically targetable vulnerability in ovarian cancer.