​駆虫薬が悪性皮膚がんの治療に有望であることを発見(Study finds pinworm medication has potential to treat aggressive skin cancer)

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2025-04-17 アリゾナ大学

アリゾナ大学がんセンターの研究により、1955年に承認されたピンワーム治療薬「ピルビニウム・パモエート」が、希少で進行の早い皮膚がん「メルケル細胞がん(MCC)」に対して有望な治療効果を示すことが明らかになりました。この薬剤はMCC細胞の増殖を抑え、神経内分泌的性質を逆転させるとともに、マウス実験でも腫瘍縮小が確認されました。作用機序としては、がんの悪性化に関与するWntシグナル伝達経路を阻害する点が注目されます。既に他のがん種でも抗腫瘍効果が示唆されており、抗寄生虫薬のがん治療薬への再利用の可能性が示されています。今後、臨床試験で効果と安全性の検証が進められます。

<関連情報>

統合的解析によりパモ酸ピルビニウムのメルケル細胞がんに対する治療可能性が明らかになった
Integrative analysis reveals therapeutic potential of pyrvinium pamoate in Merkel cell carcinoma

Jiawen Yang, James T. Lim, Paul Victor Santiago Raj, Marcelo G. Corona, Chen Chen, Hunain Khawaja, Qiong Pan, Gillian D. Paine-Murrieta, Rick G. Schnellmann, Denise J. Roe, Prafulla C. Gokhale, James A. DeCaprio, and Megha Padi
Journal of Clinical Investigation  Published: February 11, 2025
DOI:https://doi.org/10.1172/JCI177724

​駆虫薬が悪性皮膚がんの治療に有望であることを発見(Study finds pinworm medication has potential to treat aggressive skin cancer)

Merkel Cell Carcinoma (MCC) is an aggressive neuroendocrine cutaneous malignancy arising from either ultraviolet-induced mutagenesis or Merkel cell polyomavirus (MCPyV) integration. Despite extensive research, our understanding of the molecular mechanisms driving the transition from normal cells to MCC remains limited. To address this knowledge gap, we assessed the impact of inducible MCPyV T antigens on normal human fibroblasts by performing RNA-seq. Our data uncovered changes in expression and regulation of Wnt signaling pathway members. Building on this observation, we bioinformatically evaluated various Wnt pathway perturbagens for their ability to reverse the MCC gene expression signature and identified pyrvinium pamoate, an FDA-approved anthelminthic drug known for its antitumor activity in other cancers. Leveraging transcriptomic, network, and molecular analyses, we found that pyrvinium targets multiple MCC vulnerabilities. Pyrvinium not only reverses the neuroendocrine features of MCC by modulating canonical and noncanonical Wnt signaling but also inhibits cancer cell growth by activating p53-mediated apoptosis, disrupting mitochondrial function, and inducing endoplasmic reticulum stress. Finally, we demonstrated that pyrvinium reduces tumor growth in an MCC mouse xenograft model. These findings offer a deeper understanding of the role of Wnt signaling in MCC and highlight the utility of pyrvinium as a potential treatment for MCC.

有機化学・薬学
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