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Proteogenomic Characterization Reveals Subtype-Specific Therapeutic Potential for HER2-Low Breast Cancer.


ABSTRACT: The molecular heterogeneity and distinct features of HER2-low breast cancer are poorly understood, limiting their precise management. To address this issue, longitudinal multiomic profiling of HER2-low breast cancer is performed, including genomics, transcriptomics, proteomics, lactylomics, and phosphoproteomics, using 250 well-characterized samples, and identified three proteomic subtypes: PS1 (estrogen response signaling enriched), PS2 (angiogenesis enriched), and PS3 (proliferation enriched and HER2-high like). These three proteomic subtypes have distinct features and potential therapeutic strategies, namely, endocrine therapy, antiangiogenic therapy, and anti-HER2 therapy, and are validated in external datasets and PDO models. In addition, a detailed description of the genomic characteristics and a map of the lactate modification landscape of HER2-low breast cancer are provided. This research provides complementary information, reveals the molecular characteristics of HER2-low breast cancer, and suggests potential precise therapeutic strategies for patients with this type of cancer.

SUBMITTER: Xu S 

PROVIDER: S-EPMC12948274 | biostudies-literature | 2026 Feb

REPOSITORIES: biostudies-literature

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Proteogenomic Characterization Reveals Subtype-Specific Therapeutic Potential for HER2-Low Breast Cancer.

Xu Shouping S   Yu Keda K   Liu Lei L   Wang Qin Q   Wu Xiaohui X   Chen Yihai Y   Li Guozheng G   Zhang Xin X   Wei Bo B   Fu Zitong Z   Nanding Abiyasi A   Zhao Zuxianglan Z   Yang Lingbing L   Zhang Xingda X   Wang Jianyu J   Sun Wantong W   Hao Yi Y   Cheng Zhongyi Z   Cui Xiaojiang X   Wu Hao H   Pang Da D  

Advanced science (Weinheim, Baden-Wurttemberg, Germany) 20251227 12


The molecular heterogeneity and distinct features of HER2-low breast cancer are poorly understood, limiting their precise management. To address this issue, longitudinal multiomic profiling of HER2-low breast cancer is performed, including genomics, transcriptomics, proteomics, lactylomics, and phosphoproteomics, using 250 well-characterized samples, and identified three proteomic subtypes: PS1 (estrogen response signaling enriched), PS2 (angiogenesis enriched), and PS3 (proliferation enriched a  ...[more]

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