ZBED6–IGF2–PIK3C3 autophagy axis drives ccRCC progression: A multi-omics integration study

Autophagy supports clear cell renal cell carcinoma (ccRCC) progression, yet its upstream regulatory mechanisms remain to be fully defined. Integrating bulk, single-cell, and spatial transcriptomics, we identify a regulatory axis wherein the transcription factor ZBED6 activates the expression of the autophagy-initiating kinase PIK3C3 via the repression of IGF2, thereby driving pro-tumorigenic autophagy. Spatial analysis confirms the co-localization of ZBED6 and PIK3C3 in tumor tissues. Using genes associated with this axis, we develop a six-gene prognostic signature that stratifies patients with distinct survival outcomes and differential responses to immunotherapy and targeted therapy. Functional assays show that ZBED6 promotes ccRCC cell proliferation, migration, and invasion. This work elucidates a pathway governing autophagy in ccRCC and provides a framework for prognostic assessment and precision therapy.

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Publication Details

Journal
iScience
Published
2026-02-09
DOI
https://doi.org/10.1016/j.isci.2026.114952
Primary Topic
Autophagy in Disease and Therapy
Type
article
Field-Weighted Citation Impact
0.00
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article

ZBED6–IGF2–PIK3C3 autophagy axis drives ccRCC progression: A multi-omics integration study

Guandu Li, Xinxiu Ren, Xiangyu Che, Yongzheng Han et al.
iScience
Autophagy in Disease and Therapy
article

ZBED6–IGF2–PIK3C3 autophagy axis drives ccRCC progression: A multi-omics integration study

Guandu Li, Xinxiu Ren, Xiangyu Che, Yongzheng Han, Yan Liu, Xiaochen Qi, Guangzhen Wu, Jiaao Sun, Yuanxin Liu, Qifei Wang, Feng Chen
article en

Abstract

Autophagy supports clear cell renal cell carcinoma (ccRCC) progression, yet its upstream regulatory mechanisms remain to be fully defined. Integrating bulk, single-cell, and spatial transcriptomics, we identify a regulatory axis wherein the transcription factor ZBED6 activates the expression of the autophagy-initiating kinase PIK3C3 via the repression of IGF2, thereby driving pro-tumorigenic autophagy. Spatial analysis confirms the co-localization of ZBED6 and PIK3C3 in tumor tissues. Using genes associated with this axis, we develop a six-gene prognostic signature that stratifies patients with distinct survival outcomes and differential responses to immunotherapy and targeted therapy. Functional assays show that ZBED6 promotes ccRCC cell proliferation, migration, and invasion. This work elucidates a pathway governing autophagy in ccRCC and provides a framework for prognostic assessment and precision therapy.

iScienceVol. 29(3)
Dalian Medical University (CN), First Affiliated Hospital of Dalian Medical University (CN)
Openalex Percentile: Top 61%
Autophagy in Disease and Therapy
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