1. Academic Validation
  2. Naturally derived Erythrinin C targets γ-secretase signaling to suppress triple-negative breast cancer progression and reverse paclitaxel resistance

Naturally derived Erythrinin C targets γ-secretase signaling to suppress triple-negative breast cancer progression and reverse paclitaxel resistance

  • Phytomedicine. 2026 May:154:158016. doi: 10.1016/j.phymed.2026.158016.
Ke-Fan Yang 1 Di Wang 2 Kuo Yao 1 Ran Xu 1 Li-Zhi Hu 1 Yue-Yang Liu 3 Lu Zhang 4 Qian Xu 5 Xin Yang 6 Ming-Sheng Zhou 7 Hui Jia 8
Affiliations

Affiliations

  • 1 Department of Pathology and Pathophysiology, School of Basic Medical Sciences, Shenyang Medical College, Shenyang 110034, China.
  • 2 Department of Pathology, General Hospital of Northern Theater Command, Shenyang 110015, China.
  • 3 Science and Experimental Research Center of Shenyang Medical College, No 146 Huanghe North Street, Yuhong District, Shenyang City 110034, Liaoning Province, China.
  • 4 Science and Experimental Research Center of Shenyang Medical College, No 146 Huanghe North Street, Yuhong District, Shenyang City 110034, Liaoning Province, China. Electronic address: [email protected].
  • 5 Science and Experimental Research Center of Shenyang Medical College, No 146 Huanghe North Street, Yuhong District, Shenyang City 110034, Liaoning Province, China. Electronic address: [email protected].
  • 6 Department of Endocrinology, General Hospital of Northern Theater Command, Shenyang 110015, China. Electronic address: [email protected].
  • 7 Science and Experimental Research Center of Shenyang Medical College, No 146 Huanghe North Street, Yuhong District, Shenyang City 110034, Liaoning Province, China. Electronic address: [email protected].
  • 8 School of Traditional Chinese Medicine, Shenyang Medical College, No 146 Huanghe North Street, Yuhong District, Shenyang City 110034, Liaoning Province, China. Electronic address: [email protected].
Abstract

Background: Triple-negative breast Cancer (TNBC) is a highly aggressive subtype of breast Cancer. Paclitaxel (Taxol) serves as a first-line chemotherapeutic agent, but the emergence of drug resistance often limits its clinical efficacy. Bioactive compounds with Anticancer potential and reduced toxicity have thus gained increasing research interest. Erythrinin C (EC), known for its favorable drug-like properties and accessible sourcing has attracted significant attention. However, its mechanism of action and role in modulating chemotherapy resistance remain unclear.

Purpose: This study aimed to evaluate the antitumor effects of EC on TNBC both in vivo and in vitro, and to investigate its ability to reverse of drug resistance in TNBC/Taxol cells either alone or in combination with Taxol.

Methods: The crystal structure of the γ-secretase protein was obtained from the Protein Data Bank (RCSB PDB), and a pharmacophore model was constructed based on its natural small-molecule ligands. Pharmacophore-based screening was performed across traditional Chinese medicine and natural product database to identify potential drug candidates. Confirm the interaction target between EC and γ-secretase was validated, and the biological effects, genetic influences, and in vivo activity of EC targeting γ-secretase were assessed through in vitro and in vivo experiments.

Results: EC was identified as a γ-secretase Inhibitor and was shown to suppress TNBC cell proliferation and migration in vitro. Genetic modulation of PSEN-1 in MDA-MB-231 cells revealed that low PSEN-1 expression inhibits the malignant phenotype of TNBC cells. Pharmacological evaluation confirmed that EC treatment effectively slows TNBC progression. Furthermore, EC effectively reversed Taxol resistance in TNBC/Taxol cells. In vivo experiments further demonstrated that the combination of EC and Taxol significantly inhibited xenograft tumor growth.

Conclusion: EC acts as a natural γ-secretase Inhibitor that exerts significant anti-TNBC activity in both in vitro and in vivo by targeting PSEN-1 subunit. It also reverses TNBC/Taxol resistance at both cellular and animal levels, highlighting its promising and potential as a novel targeted therapeutic candidate for TNBC.

Keywords

Erythrinin C; Paclitaxel resistance; Triple-negative breast cancer; γ-secretase inhibitor.

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