Use of memantine in the preparation of a medicament for preventing and / or treating small cell lung cancer expressing grm2a

By detecting the expression of GluN2A protein in patients with small cell lung cancer, patients suitable for mimantine targeted therapy were screened, and mimantine drugs were developed, which solved the problems of recurrence and drug resistance in small cell lung cancer and achieved a highly efficient and safe targeted therapy effect.

CN122410031APending Publication Date: 2026-07-17SHENZHEN HOSPITAL CANCER HOSPITAL CHINESE ACAD OF MEDICAL SCI
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Patent Information

Application Number
CN202610665842.1
Authority / Receiving Office
CN · China
Patent Type
Applications(China)
Current Assignee / Owner
Filing Date
2026-05-14
Publication Date
2026-07-17

AI Technical Summary

Technical Problem

Current technologies lack effective targeted drugs and precise screening criteria for applicable populations, leading to severe recurrence and drug resistance in small cell lung cancer, resulting in extremely low five-year survival rates for patients. Traditional non-selective drug therapy lacks targeting and is difficult to treat effectively.

Method used

Using GluN2A protein as a biomarker, this study screens patients suitable for meimantine targeted therapy by detecting whether GluN2A protein is expressed in small cell lung cancer patient samples, and develops meimantine as a drug for the prevention and treatment of small cell lung cancer expressing GRIN2A.

Benefits of technology

It significantly inhibits the viability, clonogenic ability, DNA replication activity and migration ability of small cell lung cancer cells, destroys 3D tumor spheroids, reduces the volume and weight of xenograft tumors, improves treatment efficiency, and provides a new drug solution. It has the characteristics of strong pharmacological effects, clear targeting and good safety.

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Abstract

本发明提供了美金刚在制备预防和 / 或治疗表达GRIN2A的小细胞肺癌的药物中的应用,属于生物医药技术领域。本发明发现GluN2A蛋白是小细胞肺癌不良预后及靶向干预的重要分子标志物。另外,本发明发现美金刚、其衍生物或药用盐能够以剂量依赖的方式显著抑制小细胞肺癌细胞的活力、克隆形成能力、DNA复制活性及迁移能力,并有效破坏3D肿瘤球体的形成、诱导肿瘤细胞死亡,显著减小了小细胞肺癌异种移植瘤的体积和重量。本发明提供的伴随诊断与靶向用药策略,克服了传统非选择性用药的盲目性,为现有小细胞肺癌的治疗提供了新的药物解决方案。
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