Disruption of the sorcin‒PAX5 protein‒protein interaction induces ferroptosis by promoting the FBXL12-mediated ubiquitination of ALDH1A1 in pancreatic cancer

In this study, we revealed the mechanism of action of sorcin, which is a druggable target for inducing ferroptosis, we identified celastrol as a novel agent that induces ferroptosis, and we showed that disrupting the sorcin-PAX5 interaction is a promising therapeutic strategy for treating pancreatic cancer.

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Publication Details

Journal
Journal of Hematology & Oncology
Published
2025-03-07
DOI
https://doi.org/10.1186/s13045-025-01680-8
Citations
10
Primary Topic
Ferroptosis and cancer prognosis
Type
article
Field-Weighted Citation Impact
15.18

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article

Disruption of the sorcin‒PAX5 protein‒protein interaction induces ferroptosis by promoting the FBXL12-mediated ubiquitination of ALDH1A1 in pancreatic cancer

Shuoqian Ma, Tianyang Chen, Yahui Ding, Sisi Chen et al.
10 citations
Journal of Hematology & Oncology
Ferroptosis and cancer prognosis
15.18
article

Disruption of the sorcin‒PAX5 protein‒protein interaction induces ferroptosis by promoting the FBXL12-mediated ubiquitination of ALDH1A1 in pancreatic cancer

Shuoqian Ma, Tianyang Chen, Yahui Ding, Sisi Chen, Wanjing Feng, Quan Zhang, Yongping Bai
article en
10 citations

Abstract

In this study, we revealed the mechanism of action of sorcin, which is a druggable target for inducing ferroptosis, we identified celastrol as a novel agent that induces ferroptosis, and we showed that disrupting the sorcin-PAX5 interaction is a promising therapeutic strategy for treating pancreatic cancer.

Journal of Hematology & OncologyVol. 18(1)
Nankai University (CN), State Key Laboratory of Medicinal Chemical Biology
National Natural Science Foundation of China
Openalex Percentile: Top 1%
Ferroptosis and cancer prognosis
15.18
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