Patil R, Sun T, Chepurna O, Khoobchandani M, Rudensky S, Holler E, Ljubimova J Y, Black K L
Department of Basic Sciences and Neurosurgery, Division of Cancer Science, Loma Linda University, School of Medicine, Loma Linda, 11175 Campus St., Loma Linda, CA, 92350, USA.
Department of Neurosurgery, Cedars-Sinai Medical Center, Los Angeles, USA.
J Oncol Res Ther. 2024;9. doi: 10.29011/2574-710x.10226. Epub 2024 Jun 17.
Despite extensive efforts, glioblastoma multiforme (GBM), the most malignant brain cancer, continues to pose significant challenges to effective treatment, with limited progress in patient survival over the last three decades. This study addresses shortcomings of conventional therapies, particularly radiotherapy (RT), which faces limitations due to radio-resistance and toxic radiation doses. Boron neutron capture therapy (BNCT) is a promising alternative, delivering targeted radiation to tumor cells with minimal damage to healthy tissue. However, the key challenge lies in achieving sufficient boron uptake selectively in tumor cells. We have developed a novel nanomedicine-based approach, utilizing polymalic acid (PMLA) as a delivery vehicle, carrying multiple boron-10 molecules per nanoconjugate to increase the intracellular concentration of boron-10 for effective boron neutron capture therapy. Our novel nanodrug (Nano-Boron) incorporates isotopically enriched 4-boronophenylalanine (BPA) as a source of boron-10 and Angiopep-2 (AP2) peptide for blood-brain barrier penetration and tumor targeting. The PMLA platform allows for the attachment of a large quantity of boron-10, enhancing the intracellular boron concentration and, consequently, the efficacy of BNCT. This innovative approach holds the potential to address the unmet clinical need in GBM treatment and improve patient survival and quality of life.
尽管付出了巨大努力,多形性胶质母细胞瘤(GBM)这种最恶性的脑癌,在有效治疗方面仍然面临重大挑战,过去三十年来患者生存率进展有限。本研究旨在解决传统疗法的不足,特别是放射疗法(RT),其因放射抗性和有毒辐射剂量而面临局限性。硼中子俘获疗法(BNCT)是一种很有前景的替代方法,能将靶向辐射传递给肿瘤细胞,同时对健康组织的损伤最小。然而,关键挑战在于如何在肿瘤细胞中选择性地实现足够的硼摄取。我们开发了一种基于新型纳米药物的方法,利用聚苹果酸(PMLA)作为递送载体,每个纳米缀合物携带多个硼 - 10分子,以增加硼 - 10的细胞内浓度,从而实现有效的硼中子俘获疗法。我们的新型纳米药物(纳米硼)包含同位素富集的4 - 硼代苯丙氨酸(BPA)作为硼 - 10的来源以及血管活性肠肽 - 2(AP2)肽,用于血脑屏障穿透和肿瘤靶向。PMLA平台允许附着大量的硼 - 10,提高细胞内硼浓度,进而提高BNCT的疗效。这种创新方法有望满足GBM治疗中未满足的临床需求,并改善患者的生存率和生活质量。