硼中子俘获疗法治疗乳腺癌的研究现状

Research status of boron neutron capture therapy in the treatment of breast cancer

  • 摘要: 硼中子俘获治疗(boron neutron capture therapy,BNCT)是一种“二元靶向疗法”,结合了含硼药物与中子照射的相互作用,可在细胞水平上精准破坏肿瘤细胞。目前BNCT的临床应用主要集中于难治性恶性肿瘤,如复发转移性头颈癌、复发性脑胶质瘤和皮肤恶性黑色素瘤等。近来,多个瘤种被纳入BNCT临床试验,包括乳腺癌、肺癌。其中,4-二羟基硼基-L型苯丙氨酸(4-Borono-L-phenylalanine,BPA)可以通过L-型氨基酸转运体1(L-type amino acid transporters 1,LAT1)进入肿瘤细胞,因HER-2过表达型和三阴性乳腺癌细胞的LAT1表达水平较高,因此BNCT在难治性乳腺癌领域中显示出良好的理论基础和应用潜力。本综述旨在总结BNCT的物理和生物学基础,及其在乳腺癌基础和临床研究中的最新进展,讨论其机制、疗效及未来发展方向。

     

    Abstract: Boron neutron capture therapy (BNCT) is a “dual-targeting therapy”that combines boron-containing drug delivery with neutron irradiation to specifically destroy tumor cells at the cellular level. Current clinical applications of BNCT primarily focus on refractory malignant tumors, such as recurrent metastatic head and neck cancer, recurrent gliomas, and cutaneous malignant melanomas. Multiple tumor types, including breast and lung cancers, have recently been included in BNCT clinical trials. Among these, 4-Borono-L-phenylalanine (BPA) can enter tumor cells via L-type amino acid transporter 1 (LAT1). Elevated LAT1 expression in HER-2 overexpressing and triple-negative breast cancer cells provides a sound theoretical basis and indicates promising application potential for BPA in treating refractory breast cancer. This review summarizes the physical and biological foundations of BNCT, describes the latest advances in basic and clinical breast cancer research, and discusses mechanisms, efficacy, and future directions for BNCT research.

     

/

返回文章
返回