Evidence map›Paper›PMID 39809267›Full record

ArticleCell reports. Medicine2025

Spatial covariance reveals isothiocyanate natural products adjust redox stress to restore function in alpha-1-antitrypsin deficiency.

Shuhong Sun, Chao Wang, Junyan Hu, Pei Zhao, Xi Wang, William E Balch

Abstract read
In one paragraph

Article in Cell reports. Medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. Article
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

6 authors.

Shuhong SunDepartment of Molecular Medicine, The Scripps Research Institute, La Jolla, CA, USA; Department of Nutrition and Food Hygiene, Center for Global Health, School of Public Health, Nanjing Medical University, Nanjing 211166, China; Institute for Brain Tumors, Collaborative Innovation Center for Cancer Personalized Medicine, and Center for Global Health, Nanjing Medical University, Nanjing 211166, China. Electronic address: sunsh@njmu.edu.cn.
Chao WangDepartment of Molecular Medicine, The Scripps Research Institute, La Jolla, CA, USA; Institute of Systems and Physical Biology, Shenzhen Bay Laboratory, Shenzhen, China. Electronic address: chaowang@szbl.ac.cn.
Junyan HuDepartment of Molecular Medicine, The Scripps Research Institute, La Jolla, CA, USA.
Pei ZhaoDepartment of Molecular Medicine, The Scripps Research Institute, La Jolla, CA, USA.
Xi WangDepartment of Molecular Medicine, The Scripps Research Institute, La Jolla, CA, USA.
William E BalchDepartment of Molecular Medicine, The Scripps Research Institute, La Jolla, CA, USA. Electronic address: webalch@scripps.edu.

Funding

Tissue resident macrophages regulate proteostasis in the aging lungP01AG049665 · NIA · NORTHWESTERN UNIVERSITY AT CHICAGO · PI NAVDEEP S CHANDEL · 2015 to 2026
$26.9M
Restoration of mutant CFTR stability and functionR01DK051870 · NIDDK · UNIV OF NORTH CAROLINA CHAPEL HILL · PI BALCH, WILLIAM EDWARD · 1996 to 2020
$8.7M
Modulation of Lung Disease by Genetic/Epigenetic ProfilingR01HL095524 · NHLBI · SCRIPPS RESEARCH INSTITUTE, THE · PI William Edward Balch · 2010 to 2026
$7.5M
Using Genetic Diversity to Manage Neurological DiseaseR01AG070209 · NIA · SCRIPPS RESEARCH INSTITUTE, THE · PI BALCH, WILLIAM EDWARD · 2021 to 2025
$2.7M
Managing Alpha-1-Antitrypsin Deficiency (AATD) through Proteostasis Signaling PathwaysR01HL169631 · NHLBI · SCRIPPS RESEARCH INSTITUTE, THE · PI William Edward Balch · 2024 to 2026
$2.6M
Managing the Folding Landscape in Alpha1 Liver-Lung DiseaseR01HL141810 · NHLBI · SCRIPPS RESEARCH INSTITUTE, THE · PI BALCH, WILLIAM EDWARD · 2018 to 2021
$1.9M
Applying Spatial Covariance to Understand Human Variation in Genetic DiseaseR01HL166410 · NHLBI · SCRIPPS RESEARCH INSTITUTE, THE · PI William Edward Balch · 2023 to 2026
$1.8M
NHLBI NIH HHS R01 HL095524NHLBI NIH HHS R01 HL141810NHLBI NIH HHS R01 HL166410NHLBI NIH HHS R01 HL169631NIA NIH HHS P01 AG049665NIA NIH HHS R01 AG070209NIDDK NIH HHS R01 DK051870
6 · The paper itself

Abstract

Alpha-1 antitrypsin (AAT) deficiency (AATD) is a monogenic disease caused by misfolding of AAT variants resulting in gain-of-toxic aggregation in the liver and loss of monomer activity in the lung leading to chronic obstructive pulmonary disease (COPD). Using high-throughput screening, we discovered a bioactive natural product, phenethyl isothiocyanate (PEITC), highly enriched in cruciferous vegetables, including watercress and broccoli, which improves the level of monomer secretion and neutrophil elastase (NE) inhibitory activity of AAT-Z through the endoplasmic reticulum (ER) redox sensor protein disulfide isomerase (PDI) A4 (PDIA4). The intracellular polymer burden of AAT-Z can be managed by combination treatment of PEITC and an autophagy activator. Using Gaussian process (GP)-based spatial covariance (SCV) (GP-SCV) machine learning to map on a residue-by-residue basis at atomic resolution all variants in the worldwide AATD clinical population, we reveal a global rescue of monomer secretion and NE inhibitory activity for most variants triggering disease. We present a proof of concept that GP-SCV mapping of restoration of AAT variant function serves as a standard model to discover natural products such as the anti-oxidant PEITC that could potentially impact the redox/inflammatory environment of the ER to provide a nutraceutical approach to help minimize disease in AATD patients.

Indexed as

alpha 1-Antitrypsinalpha 1-Antitrypsin DeficiencyBiological ProductsIsothiocyanatesEndoplasmic ReticulumHumansOxidation-ReductionProtein Disulfide-Isomerasesalpha 1-AntitrypsinBiological ProductsIsothiocyanatesphenethyl isothiocyanateProtein Disulfide-IsomerasesAATDalpha-1 antitrypsin deficiencychronic obstructive pulmonary diseaseCOPDGaussian process machine learninggenetic variationisothiocyanatenutraceuticaloxidative stressPDIA4protein aggregationprotein disulfide isomerase A4proteostasis

Identifiers

PMID39809267
PMCPMC11866504

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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.