Evidence map›Paper›PMID 37884806›Full record

ArticleNature chemical biology2024

A genetically encoded tool to increase cellular NADH/NAD

Xingxiu Pan, Mina L Heacock, Evana N Abdulaziz, Sara Violante, Austin L Zuckerman, Nirajan Shrestha, Canglin Yao, Russell P Goodman, Justin R Cross, Valentin Cracan

Abstract read
In one paragraph

Article in Nature chemical biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

30 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Biomarkers of Cardiac Metabolic Flexibility in Health, HFrEF and HFpEF.International journal of molecular sciences · 2026
    Review
  11. Article
  12. Changes in the brain [NADFrontiers in aging neuroscience · 2026
    Review
  13. The energy resistance principle.Cell metabolism · 2025
    Review
  14. An acyltransferase protectsbioRxiv : the preprint server for biology · 2025
    Article
  15. Article
  16. Nanomedicine-Driven Modulation of Reductive Stress for Cancer Therapy.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Review
  17. Review
  18. Article
  19. Article
  20. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Xingxiu Pan *Laboratory of Redox Biology and Metabolism, Scintillon Institute, San Diego, CA, USA.
Mina L Heacock *Laboratory of Redox Biology and Metabolism, Scintillon Institute, San Diego, CA, USA.
Evana N Abdulaziz *Laboratory of Redox Biology and Metabolism, Scintillon Institute, San Diego, CA, USA.
Sara ViolanteDonald B. and Catherine C. Marron Cancer Metabolism Center, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Austin L ZuckermanLaboratory of Redox Biology and Metabolism, Scintillon Institute, San Diego, CA, USA.
Nirajan ShresthaLiver Center, Division of Gastroenterology, Massachusetts General Hospital, Boston, MA, USA.ORCID http://orcid.org/0000-0003-1259-0661
Canglin YaoLaboratory of Redox Biology and Metabolism, Scintillon Institute, San Diego, CA, USA.
Russell P GoodmanLiver Center, Division of Gastroenterology, Massachusetts General Hospital, Boston, MA, USA.
Justin R CrossDonald B. and Catherine C. Marron Cancer Metabolism Center, Memorial Sloan Kettering Cancer Center, New York, NY, USA.ORCID http://orcid.org/0000-0002-6356-057X
Valentin CracanLaboratory of Redox Biology and Metabolism, Scintillon Institute, San Diego, CA, USA. vcracan@scripps.edu.ORCID http://orcid.org/0000-0002-3280-0593

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
Expanding the set of genetically encoded tools for compartment-specific manipulation of redox metabolism in living cellsR35GM142495 · NIGMS · SCINTILLON INSTITUTE FOR PHOTOBIOLOGY · PI Valentin Cracan · 2021 to 2026
$3.2M
An NADH-ChREBP axis in fatty liver disease and dyslipidemiaR01DK134675 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI Russell Paul Goodman · 2023 to 2026
$2.0M
Engineered flavin-dependent enzymes for probing redox environment and regulationR00GM121856 · NIGMS · SCINTILLON INSTITUTE FOR PHOTOBIOLOGY · PI CRACAN, VALENTIN · 2019 to 2021
$747k
Defining and targeting the compartmentalization of redox metabolism in aging using novel genetically encoded toolsR03AG067301 · NIA · SCINTILLON INSTITUTE FOR PHOTOBIOLOGY · PI CRACAN, VALENTIN · 2020 to 2021
$192k
Seahorse XF96 Extracellular Flux AnalyzerS10OD016357 · OD · SCRIPPS RESEARCH INSTITUTE, THE · PI SAEZ, ENRIQUE · 2013 to 2013
$175k
NCI NIH HHS P30 CA008748NIA NIH HHS R03 AG067301NIDDK NIH HHS R01 DK134675NIGMS NIH HHS R00 GM121856NIGMS NIH HHS R35 GM142495NIH HHS S10 OD016357
6 · The paper itself

Abstract

Impaired redox metabolism is a key contributor to the etiology of many diseases, including primary mitochondrial disorders, cancer, neurodegeneration and aging. However, mechanistic studies of redox imbalance remain challenging due to limited strategies that can perturb redox metabolism in various cellular or organismal backgrounds. Most studies involving impaired redox metabolism have focused on oxidative stress; consequently, less is known about the settings where there is an overabundance of NADH reducing equivalents, termed reductive stress. Here we introduce a soluble transhydrogenase from Escherichia coli (EcSTH) as a novel genetically encoded tool to promote reductive stress in living cells. When expressed in mammalian cells, EcSTH, and a mitochondrially targeted version (mitoEcSTH), robustly elevated the NADH/NAD

Indexed as

Escherichia coliNADOxidation-ReductionEscherichia coli ProteinsHEK293 CellsHumansMitochondriaNADP TranshydrogenasesOxidative StressEscherichia coli ProteinsNADNADP Transhydrogenases

Identifiers

PMID37884806
PMCPMC11045668

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.