Cuproptosis and Disulfidptosis Converge to Empower PD‐L1 Checkpoint Therapy via Cadict‐Induced PD‐L1 Translation

Immune checkpoint blockade (ICB) has emerged as a cornerstone of cancer therapy, yet its effectiveness remains restricted in PD-L1-low malignancies due to insufficient target expression. We herein develop the cuproptosis and disulfidptosis co-delivery targeted (Cadict) nanodrug, an epidermal growth factor receptor (EGFR)-targeted nanoplatform designed to co-induce cuproptosis and disulfidptosis, thereby synergistically augmenting tumor cytotoxicity and sensitizing cancers to anti-PD-L1 therapy. Cadict exploits copper-sulfur (Cu-S) coordination chemistry to co-deliver copper ions and cystine, while integrating glucose oxidase (GOx) to create a hypoglycemic milieu essential for disulfidptosis execution. This dual cytotoxic mechanism not only triggers immunogenic cell death-like phenotype but also unexpectedly activates the integrated stress response (ISR), promoting PD-L1 upregulation through Eif5b-dependent translation. The resulting synergy between redox-driven cytotoxicity and immune modulation potentiates anti-PD-L1 efficacy, leading to robust tumor regression and durable immunological memory. Our work presents a seminal strategy that leverages tumor redox vulnerabilities to advance cancer immunotherapy, providing a new paradigm for overcoming ICB resistance via targeted tumor sensitization.

Authors

Institutions

Publication Details

Journal
Advanced Science
Published
2026-02-21
DOI
https://doi.org/10.1002/advs.202515367
Primary Topic
Nanoplatforms for cancer theranostics
Type
article
Field-Weighted Citation Impact
0.00

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Cuproptosis and Disulfidptosis Converge to Empower PD‐L1 Checkpoint Therapy via Cadict‐Induced PD‐L1 Translation

Wenbin He, Qinghai Li, Xiaoxue Wu, Sicong Huang et al.
Advanced Science
Nanoplatforms for cancer theranostics
article

Cuproptosis and Disulfidptosis Converge to Empower PD‐L1 Checkpoint Therapy via Cadict‐Induced PD‐L1 Translation

Wenbin He, Qinghai Li, Xiaoxue Wu, Sicong Huang, Mei Song, Lulu Chen, Xiaoting Liu, Ruihan Pu, J W Gao, Qi Zhou, Shiyao Song, Xinhua Zhang, Jiatong Dai
article en

Abstract

Immune checkpoint blockade (ICB) has emerged as a cornerstone of cancer therapy, yet its effectiveness remains restricted in PD-L1-low malignancies due to insufficient target expression. We herein develop the cuproptosis and disulfidptosis co-delivery targeted (Cadict) nanodrug, an epidermal growth factor receptor (EGFR)-targeted nanoplatform designed to co-induce cuproptosis and disulfidptosis, thereby synergistically augmenting tumor cytotoxicity and sensitizing cancers to anti-PD-L1 therapy. Cadict exploits copper-sulfur (Cu-S) coordination chemistry to co-deliver copper ions and cystine, while integrating glucose oxidase (GOx) to create a hypoglycemic milieu essential for disulfidptosis execution. This dual cytotoxic mechanism not only triggers immunogenic cell death-like phenotype but also unexpectedly activates the integrated stress response (ISR), promoting PD-L1 upregulation through Eif5b-dependent translation. The resulting synergy between redox-driven cytotoxicity and immune modulation potentiates anti-PD-L1 efficacy, leading to robust tumor regression and durable immunological memory. Our work presents a seminal strategy that leverages tumor redox vulnerabilities to advance cancer immunotherapy, providing a new paradigm for overcoming ICB resistance via targeted tumor sensitization.

Advanced Science
Sun Yat-sen University (CN), Xiamen University (CN), First Affiliated Hospital of Xiamen University (CN), Zhongshan Hospital of Xiamen University (CN), The First Affiliated Hospital, Sun Yat-sen University (CN)
National Natural Science Foundation of China, Natural Science Foundation of Fujian Province, Basic and Applied Basic Research Foundation of Guangdong Province
Openalex Percentile: Top 48%
Nanoplatforms for cancer theranostics
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.