Marked for destruction? When S -nitrosylation writes protein fate through metabolic rewiring

Metabolism and autophagy are closely interconnected, but whether metabolic alterations can chemically modify proteins and influence their selective autophagic degradation remains poorly understood. Our recent findings show that increased S-nitrosylation resulting from the loss of the denitrosylase AKR1A1/SCoR impairs glycolysis and promotes methylglyoxal accumulation, leading to carbonyl modification and selective autophagic degradation of KEAP1. These findings suggest that metabolic rewiring can influence the fate of specific proteins. In particular, we discuss whether glycation may act as a metabolic “mark” for selective autophagy and how the removal of metabolically modified proteins may, in turn, sustain signaling pathways involved in tumor progression and therapy resistance

Authors

Institutions

Publication Details

Journal
Autophagy
Published
2026-09-16
DOI
https://doi.org/10.1080/15548627.2026.2735183
Primary Topic
Redox biology and oxidative stress
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
article

Marked for destruction? When S -nitrosylation writes protein fate through metabolic rewiring

Giuseppe Filomeni, Chiara Pecorari
Autophagy
Redox biology and oxidative stress
article

Marked for destruction? When S -nitrosylation writes protein fate through metabolic rewiring

Giuseppe Filomeni, Chiara Pecorari
article en

Abstract

Metabolism and autophagy are closely interconnected, but whether metabolic alterations can chemically modify proteins and influence their selective autophagic degradation remains poorly understood. Our recent findings show that increased S-nitrosylation resulting from the loss of the denitrosylase AKR1A1/SCoR impairs glycolysis and promotes methylglyoxal accumulation, leading to carbonyl modification and selective autophagic degradation of KEAP1. These findings suggest that metabolic rewiring can influence the fate of specific proteins. In particular, we discuss whether glycation may act as a metabolic “mark” for selective autophagy and how the removal of metabolically modified proteins may, in turn, sustain signaling pathways involved in tumor progression and therapy resistance

Autophagy
University of Rome Tor Vergata (IT), Cancer Institute (WIA) (IN), Danish Cancer Society (DK)
Zero hunger
Openalex Percentile: Top 18%
Redox biology and oxidative stress
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.

Marked for destruction? When S -nitrosylation writes protein fate through metabolic rewiring — Giuseppe Filomeni, Chiara Pecorari · Autophagy (2026) | TGRS Research Map | TGRS