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March 15, 2026Current Molecular Pharmacology2 citationsOpen Access

Gramine suppresses triple-negative breast cancer by inducing ferroptosis via CUL3-mediated ubiquitination of MTDH

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SZShangjun ZhouXZXudong ZhuZXZhijie Xu

Key Points

  • The aim is to explore the therapeutic potential of gramine in treating triple-negative breast cancer (TNBC) and understand its mechanisms.
  • Screened 27 indole alkaloids using CCK-8 assays.
  • Applied LIP-MS, molecular docking, CETSA, and DARTS assays to validate target binding.
  • Conducted Western blot to assess expression of MTDH, SLC3A2, GPX4.
  • Used ferroptosis rescue and MTDH knockdown to confirm mechanism.
  • Conducted in vivo efficacy studies using 4T1 and MDA-MB-231 xenograft mouse models.
  • Gramine selectively inhibited TNBC cell growth with an IC₅₀ of approximately 22–28 µM.
  • Identified MTDH as a key effector in regulating ferroptosis pathways.
  • Gramine bound directly to CUL3, reducing its activity toward MTDH, leading to increased ferroptosis markers.
  • GM suppressed tumor growth in vivo without significant systemic toxicity.

Abstract

Triple-negative breast cancer (TNBC) is a highly aggressive subtype of breast cancer lacking effective targeted therapies and frequently exhibiting chemotherapy resistance. Natural compounds are valued for their multi-target therapeutic potential and lower toxicity profiles. This study explores gramine (GM) as a potential candidate for TNBC treatment and investigates its mechanism of action. We screened 27 indole alkaloids via CCK-8 assays. LIP-MS, molecular docking, CETSA, and DARTS assays validated direct binding to candidate targets. Expression of MTDH, SLC3A2, GPX4 was assessed by Western blot. Ferroptosis markers and mitochondrial morphology were measured. Ferroptosis rescue and MTDH knockdown were used to confirm mechanism. In vivo efficacy was assessed by 4T1 and MDA-MB-231 xenograft mouse models. GM selectively inhibited TNBC cell growth (IC₅₀ ∼ 22–28 µM). Proteomic analysis revealed the involvement of ferroptosis pathways and identified MTDH as a key effector. GM directly bound to CUL3, reducing its E3 ubiquitin ligase activity toward MTDH, thereby stabilizing MTDH, which downregulated ferroptosis inhibitors (SLC3A2, GPX4) and upregulated ferroptosis markers (ROS, Fe²⁺, and MDA), along with decreased GSH and mitochondrial morphological changes. Ferroptosis rescue or MTDH knockdown significantly reversed GM’s anti-TNBC effects both in vivo and in vitro . Furthermore, GM markedly suppressed tumor growth in vivo without obvious systemic toxicity. GM inhibits TNBC growth by targeting the CUL3–MTDH axis to trigger ferroptosis. This study uncovers a novel regulatory pathway in ferroptosis, highlighting the significant potential of GM as an effective therapeutic candidate for TNBC.

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Cite This Study

Zhou et al. (2026) studied this question.

synapsesocial.com/papers/69b64d48b42794e3e660e11chttps://doi.org/10.1016/j.cmp.2026.03.001
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