钙和 CACNA1H 通过 AM RF EMF 介导对乳腺癌脑转移的靶向抑制。

Ca and CACNA1H mediate targeted suppression of breast cancer brain metastasis by AM RF EMF.

机构信息

Department of Cancer Biology, Wake Forest Baptist Medical Center, Winston-Salem, NC, United States of America.

Department of Radiation Oncology, Wake Forest Baptist Medical Center, Winston-Salem, NC, United States of America.

出版信息

EBioMedicine. 2019 Jun;44:194-208. doi: 10.1016/j.ebiom.2019.05.038. Epub 2019 May 23.

Abstract

BACKGROUND

Brain metastases are a major cause of death in patients with metastatic breast cancer. While surgical resection and radiation therapy are effective treatment modalities, the majority of patients will succumb from disease progression. We have developed a novel therapy for brain metastases that delivers athermal radiofrequency electromagnetic fields that are amplitude-modulated at breast cancer specific frequencies (BCF).

METHODS

27.12 MHz amplitude-modulated BCF were administered to a patient with a breast cancer brain metastasis by placing a spoon-shaped antenna on the anterior part of the tongue for three one-hour treatments every day. In preclinical models, a BCF dose, equivalent to that delivered to the patient's brain, was administered to animals implanted with either brain metastasis patient derived xenografts (PDXs) or brain-tropic cell lines. We also examined the efficacy of combining radiation therapy with BCF treatment. Additionally, the mechanistic underpinnings associated with cancer inhibition was identified using an agnostic approach.

FINDINGS

Animal studies demonstrated a significant decrease in growth and metastases of brain-tropic cell lines. Moreover, BCF treatment of PDXs established from patients with brain metastases showed strong suppression of their growth ability. Importantly, BCF treatment led to significant and durable regression of brain metastasis of a patient with triple negative breast cancer. The tumour inhibitory effect was mediated by Ca influx in cancer cells through CACNA1H T-type voltage-gated calcium channels, which, acting as the cellular antenna for BCF, activated CAMKII/p38 MAPK signalling and inhibited cancer stem cells through suppression of β-catenin/HMGA2 signalling. Furthermore, BCF treatment downregulated exosomal miR-1246 level, which in turn decreased angiogenesis in brain environment. Therefore, targeted growth inhibition of breast cancer metastases was achieved through CACNA1H.

INTERPRETATION

We demonstrate that BCF, as a single agent or in combination with radiation, is a novel treatment approach to the treatment of brain metastases. This paradigm shifting modality warrants further clinical trials for this unmet medical need.

摘要

背景

脑转移是转移性乳腺癌患者死亡的主要原因。虽然手术切除和放射治疗是有效的治疗方法,但大多数患者仍会因疾病进展而死亡。我们开发了一种治疗脑转移的新方法,该方法通过在前舌部放置一个汤匙形天线,施加幅度调制在乳腺癌特定频率(BCF)的无热射频电磁场。

方法

对一名患有乳腺癌脑转移的患者,每天进行三次、每次一小时的治疗,将汤匙形天线放在舌前部分,施加 27.12MHz 幅度调制的 BCF。在临床前模型中,将相当于患者大脑所接受的 BCF 剂量,施加到植入脑转移患者来源异种移植物(PDX)或脑趋向性细胞系的动物中。我们还研究了与 BCF 治疗相结合的放射治疗的疗效。此外,使用一种非特定的方法确定了与癌症抑制相关的机制基础。

发现

动物研究表明,脑趋向性细胞系的生长和转移明显减少。此外,对来自脑转移患者的 PDX 进行 BCF 治疗显示出强烈抑制其生长能力。重要的是,BCF 治疗导致一名三阴性乳腺癌患者脑转移的显著和持久消退。肿瘤抑制作用是通过 CACNA1H T 型电压门控钙通道介导的癌细胞内钙流入介导的,该通道作为 BCF 的细胞天线,激活 CAMKII/p38 MAPK 信号通路,并通过抑制 β-连环蛋白/HMGA2 信号通路抑制癌症干细胞。此外,BCF 治疗下调了外泌体 miR-1246 水平,进而减少了脑环境中的血管生成。因此,通过 CACNA1H 实现了对乳腺癌转移的靶向生长抑制。

解释

我们证明 BCF 作为单一药物或与放射治疗联合使用,是治疗脑转移的一种新的治疗方法。这种改变范式的模式为这一未满足的医疗需求进一步的临床试验提供了依据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a58/6604768/2a83906dca9c/gr1.jpg

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