Nicotinamide (niacin) supplement increases lipid metabolism and ROS‐induced energy disruption in triple‐negative breast cancer: potential for drug repositioning as an anti‐tumor agent. Issue 9 (25th March 2022)
- Record Type:
- Journal Article
- Title:
- Nicotinamide (niacin) supplement increases lipid metabolism and ROS‐induced energy disruption in triple‐negative breast cancer: potential for drug repositioning as an anti‐tumor agent. Issue 9 (25th March 2022)
- Main Title:
- Nicotinamide (niacin) supplement increases lipid metabolism and ROS‐induced energy disruption in triple‐negative breast cancer: potential for drug repositioning as an anti‐tumor agent
- Authors:
- Jung, Minsun
Lee, Kyung‐Min
Im, Yebin
Seok, Seung Hyeok
Chung, Hyewon
Kim, Da Young
Han, Dohyun
Lee, Cheng Hyun
Hwang, Eun Hye
Park, Soo Young
Koh, Jiwon
Kim, Bohyun
Nikas, Ilias P.
Lee, Hyebin
Hwang, Daehee
Ryu, Han Suk - Abstract:
- Abstract : Metabolic dysregulation is an important hallmark of cancer. Nicotinamide (NAM), a water‐soluble amide form of niacin (vitamin B3), is currently available as a supplement for maintaining general physiologic functions. NAM is a crucial regulator of mitochondrial metabolism and redox reactions. In this study, we aimed to identify the mechanistic link between NAM‐induced metabolic regulation and the therapeutic efficacy of NAM in triple‐negative breast cancer (TNBC). The combined analysis using multiomics systems biology showed that NAM decreased mitochondrial membrane potential and ATP production, but increased the activities of reverse electron transport (RET), fatty acid β‐oxidation and glycerophospholipid/sphingolipid metabolic pathways in TNBC, collectively leading to an increase in the levels of reactive oxygen species (ROS). The increased ROS levels triggered apoptosis and suppressed tumour growth and metastasis of TNBC in both human organoids and xenograft mouse models. Our results showed that NAM treatment leads to cancer cell death in TNBC via mitochondrial dysfunction and activation of ROS by bifurcating metabolic pathways (RET and lipid metabolism); this provides insights into the repositioning of NAM supplement as a next‐generation anti‐metabolic agent for TNBC treatment. Abstract : Nicotinamide is a niacin (vitamin B3) supplement. Using multiomics systems biology, we showed that nicotinamide increased the activities of reverse electron transport (RET)Abstract : Metabolic dysregulation is an important hallmark of cancer. Nicotinamide (NAM), a water‐soluble amide form of niacin (vitamin B3), is currently available as a supplement for maintaining general physiologic functions. NAM is a crucial regulator of mitochondrial metabolism and redox reactions. In this study, we aimed to identify the mechanistic link between NAM‐induced metabolic regulation and the therapeutic efficacy of NAM in triple‐negative breast cancer (TNBC). The combined analysis using multiomics systems biology showed that NAM decreased mitochondrial membrane potential and ATP production, but increased the activities of reverse electron transport (RET), fatty acid β‐oxidation and glycerophospholipid/sphingolipid metabolic pathways in TNBC, collectively leading to an increase in the levels of reactive oxygen species (ROS). The increased ROS levels triggered apoptosis and suppressed tumour growth and metastasis of TNBC in both human organoids and xenograft mouse models. Our results showed that NAM treatment leads to cancer cell death in TNBC via mitochondrial dysfunction and activation of ROS by bifurcating metabolic pathways (RET and lipid metabolism); this provides insights into the repositioning of NAM supplement as a next‐generation anti‐metabolic agent for TNBC treatment. Abstract : Nicotinamide is a niacin (vitamin B3) supplement. Using multiomics systems biology, we showed that nicotinamide increased the activities of reverse electron transport (RET) and lipid metabolic pathways in triple‐negative breast cancer (TNBC), collectively leading to an increase in reactive oxygen species (ROS) levels. The increased ROS level suppressed tumor growth and metastasis in human organoids and xenograft mouse models. … (more)
- Is Part Of:
- Molecular oncology. Volume 16:Issue 9(2022)
- Journal:
- Molecular oncology
- Issue:
- Volume 16:Issue 9(2022)
- Issue Display:
- Volume 16, Issue 9 (2022)
- Year:
- 2022
- Volume:
- 16
- Issue:
- 9
- Issue Sort Value:
- 2022-0016-0009-0000
- Page Start:
- 1795
- Page End:
- 1815
- Publication Date:
- 2022-03-25
- Subjects:
- metabolism -- nicotinamide -- organoids -- proteogenomics -- reactive oxygen species -- triple negative breast neoplasms
Cancer -- Molecular aspects -- Periodicals
616.994005 - Journal URLs:
- http://www.journals.elsevier.com/molecular-oncology/ ↗
http://febs.onlinelibrary.wiley.com/hub/journal/10.1002/(ISSN)1878-0261/issues/ ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1002/1878-0261.13209 ↗
- Languages:
- English
- ISSNs:
- 1574-7891
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5900.817993
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- 21374.xml