LRPPRC confers enhanced oxidative phosphorylation metabolism in triple-negative breast cancer and represents a therapeutic target

This work demonstrated a new regulatory pathway of TNBC to promote the expression of mitochondrial genes by upregulating the nuclear gene LRPPRC, resulting in increased OXPHOS. We also suggested a promising therapeutic target LRPPRC for TNBC, and its inhibitor, the traditional gynecological medicine GAA, presented significant antitumor activity.

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Publication Details

Journal
Journal of Translational Medicine
Published
2025-03-25
DOI
https://doi.org/10.1186/s12967-024-05946-6
Citations
11
Primary Topic
Cancer, Hypoxia, and Metabolism
Type
article
Field-Weighted Citation Impact
10.30

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article

LRPPRC confers enhanced oxidative phosphorylation metabolism in triple-negative breast cancer and represents a therapeutic target

Dachi Wang, Q. K. Xue, Xiangsheng Liu, Xiaohong Fang et al.
11 citations
Journal of Translational Medicine
Cancer, Hypoxia, and Metabolism
10.30
article

LRPPRC confers enhanced oxidative phosphorylation metabolism in triple-negative breast cancer and represents a therapeutic target

Dachi Wang, Q. K. Xue, Xiangsheng Liu, Xiaohong Fang, Tianyu Zhang, Wenxi Wang, Xiying Shao, Wei Zhou, Tingting Shen, Xiaojia Wang, Jie Liu
article en
11 citations

Abstract

This work demonstrated a new regulatory pathway of TNBC to promote the expression of mitochondrial genes by upregulating the nuclear gene LRPPRC, resulting in increased OXPHOS. We also suggested a promising therapeutic target LRPPRC for TNBC, and its inhibitor, the traditional gynecological medicine GAA, presented significant antitumor activity.

Journal of Translational MedicineVol. 23(1)
Chinese Academy of Sciences (CN), Institute of Computing Technology (CN), Zhejiang Cancer Hospital (CN), Hangzhou Academy of Agricultural Sciences (CN), Institute of Chemistry (CN), University of Chinese Academy of Sciences (CN)
National Natural Science Foundation of China
Openalex Percentile: Top 1%
Cancer, Hypoxia, and Metabolism
10.30
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