Scientific Reports (Jul 2024)

Novel insight into nicotinamide adenine dinucleotide and related metabolites in cancer patients undergoing surgery

  • Hiroaki Fujita,
  • Taiichi Wakiya,
  • Yota Tatara,
  • Keinosuke Ishido,
  • Yoshiyuki Sakamoto,
  • Norihisa Kimura,
  • Hajime Morohashi,
  • Takuya Miura,
  • Takahiro Muroya,
  • Harue Akasaka,
  • Hiroshi Yokoyama,
  • Taishu Kanda,
  • Shunsuke Kubota,
  • Aika Ichisawa,
  • Kenta Ogasawara,
  • Daisuke Kuwata,
  • Yoshiya Takahashi,
  • Akie Nakamura,
  • Keisuke Yamazaki,
  • Takahiro Yamada,
  • Ryo Matsuyama,
  • Masanobu Kanou,
  • Kei Yamana,
  • Ken Itoh,
  • Kenichi Hakamada

DOI
https://doi.org/10.1038/s41598-024-66004-1
Journal volume & issue
Vol. 14, no. 1
pp. 1 – 11

Abstract

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Abstract Nicotinamide adenine dinucleotide (NAD +) plays a pivotal role in numerous cellular functions. Reduced NAD + levels are postulated to be associated with cancer. As interest in understanding NAD + dynamics in cancer patients with therapeutic applications in mind grows, there remains a shortage of comprehensive data. This study delves into NAD + dynamics in patients undergoing surgery for different digestive system cancers. This prospective study enrolled 99 patients with eight different cancers. Fasting blood samples were obtained during the perioperative period. The concentrations of NAD + , nicotinamide mononucleotide (NMN), and nicotinamide riboside were analyzed using tandem mass spectrometry. After erythrocyte volume adjustment, NAD + remained relatively stable after surgery. Meanwhile, NMN decreased the day after surgery and displayed a recovery trend. Interestingly, liver and pancreatic cancer patients exhibited poor postoperative NMN recovery, suggesting a potential cancer type-specific influence on NAD + metabolism. This study illuminated the behavior of NAD + in surgically treated cancer patients. We identified which cancer types have particularly low levels and at what point depletion occurs during the perioperative period. These insights suggest the need for personalized NAD + supplementation strategies, calibrated to individual patient needs and treatment timelines. Clinical trial registration jRCT1020210066.

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