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Study 1 of 47NAD+ (Nicotinamide Adenine Dinucleotide) literaturePubMed · Observational2026

Nicotinamide riboside enhances the efficacy of gemcitabine and suppresses PDAC premalignant lesions via SIRT3 activation.

Nicotinamide riboside may enhance the effectiveness of chemotherapy and delay tumor progression in pancreatic cancer models, but direct implications for human treatment remain unclear.

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Where it sits

this study against the rest of the nad+ (nicotinamide adenine dinucleotide) corpus
17
Preclinical
23
Observational · this one
1
Open-label
1
Randomised
5
Reviews

Summary and findings

This study investigates the effects of nicotinamide riboside (NR), a NAD+ precursor, on pancreatic ductal adenocarcinoma (PDAC) by assessing its role in enhancing chemosensitivity and suppressing tumor progression. The research includes multi-level clinical analyses and spontaneous PDAC models. Not reported in abstract.

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Not reported in abstract.2026

Abstract

The authors’ words, as PubMed supplied them

Pancreatic ductal adenocarcinoma (PDAC) remains a lethal malignancy with limited therapeutic options. This study identifies nicotinamide riboside (NR), a natural NAD+ precursor, as a dual-function agent that enhances chemosensitivity and suppresses tumor progression by activating the mitochondrial deacetylase sirtuin 3 (SIRT3). Multi-level clinical analyses revealed progressive SIRT3 downregulation in PDAC pathogenesis, correlating with poor survival. Genetic ablation of SIRT3 accelerated premalignant lesions in spontaneous models, whereas NR administration restored SIRT3 expression and activated its mitochondrial regulatory network, comprising key metabolic enzymes and respiratory chain components, in a SIRT3-dependent manner. In spontaneous PDAC models, NR monotherapy delayed carcinogenesis by suppressing the progression of premalignant lesions. Moreover, NR significantly potentiated gemcitabine efficacy both in vitro and in subcutaneous PDAC models, demonstrating synergistic enhancement of chemotherapy-induced tumor cell death. These findings establish NR as a promising SIRT3-targeting adjuvant that both enhances the efficacy of standard chemotherapy and delays carcinogenesis, thereby overcoming therapeutic resistance in established PDAC and potentially impeding its development.

Background

The paper addresses the potential role of nicotinamide riboside in enhancing chemotherapy efficacy and its impact on PDAC premalignant lesions. Prior research has suggested that SIRT3 may play a role in cancer metabolism and progression. This study is significant as it explores a novel approach to improve treatment outcomes in PDAC.

Methods

Not reported in abstract.

Results

Not reported in abstract.

Interpretation

Not reported in abstract.

Key findings

  • Not reported in abstract.
  • Not reported in abstract.
  • Not reported in abstract.

Limitations

  • Not reported in abstract.

Elsewhere in the NAD+ (Nicotinamide Adenine Dinucleotide) corpus

CBioactive vitamin E-NAD<sup>+</sup> conjugate nanoparticles for osteoarthritis management via simultaneous suppression of inflammation and oxidative stress.Biomaterials · 2026 · Not reported in abstract.AnimalBNAD metabolism mediates a sex-specific protection against early life infectionsbiorxiv-preprint · 2026 · Higher birth NAD levels in females were associated with reduced infection burdens during the first 3 years of life.HumanBControl-referenced bacterial bioluminescence reveals a two-axis salivary response phenotype in benign and malignant breast disease.Talanta · 2026 · n=200 · Not reported in abstract.HumanBGenetic modulation of NAD(P)H homeostasis reveals distinct redox-coupled metabolic vulnerabilities.Nature metabolism · 2026 · Not reported in abstract.HumanDA context-dependent framework for targeting NAD metabolism in cancer.Cell metabolism · 2026reviewBPart 1 of a 2-part, open-label clinical trial evaluating repeated nicotinamide riboside parenteral administration: 3 consecutive days of intramuscular and subcutaneous injectionsbiorxiv-preprint · 2026 · 9.97% average daily increase in NAD+ for 100 mg IM.Human