Robinson Prema, Coveñas Rafael, Muñoz Miguel
Department of Infectious Diseases, Infection Control and Employee Health, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
Institute of Neurosciences of Castilla y León (INCYL), Laboratory of Neuroanatomy of the Peptidergic Systems, University of Salamanca, Salamanca, Spain.
Curr Med Chem. 2023;30(16):1798-1812. doi: 10.2174/0929867329666220811152602.
Although chemotherapy is predominantly used for cancer treatment, it can be ineffective and can induce serious side effects and lead to chemoresistance. It is essential to discover novel drugs that can enhance the antitumor activity and at the same time, counteract the severe side effects, of chemotherapy. The substance P (SP)/neurokinin-1 receptor (NK-1R) interaction system is known to play a key role in the pathogenesis of cancer. Studies with NK-1R antagonists (such as aprepitant) denote that the NK-1R is a potential target for the treatment of cancer. Aprepitant combined with major chemotherapeutic drugs has shown the potential to increase antitumor activity and decrease side effects.
Since malignant tumor cancer cells overexpress the NK-1R, this combination therapy is a promising approach for the treatment of all kinds of cancer. Since aprepitant shows potential of being a broad-antitumor drug, the repurposing of this NK-1R antagonist as an antitumor agent is warranted. Studies pertaining to combination therapy of aprepitant/radiotherapy will also be outlined in this review. The aim of this review is to provide an update on combinational studies pertaining to chemotherapy/radiotherapy and NK-1R antagonist in cancer.
This combination strategy once confirmed, might open the door to a new era in chemotherapy and radiotherapy with greater antitumor activity and fewer side effects. This treatment strategy could possibly translate into higher cure rates, better quality of life and fewer sequelae in cancer patients.
尽管化疗主要用于癌症治疗,但它可能无效,会引发严重副作用并导致化疗耐药性。发现能增强化疗抗肿瘤活性并同时抵消其严重副作用的新型药物至关重要。已知P物质(SP)/神经激肽-1受体(NK-1R)相互作用系统在癌症发病机制中起关键作用。对NK-1R拮抗剂(如阿瑞匹坦)的研究表明,NK-1R是癌症治疗的一个潜在靶点。阿瑞匹坦与主要化疗药物联合使用已显示出增加抗肿瘤活性和减少副作用的潜力。
由于恶性肿瘤癌细胞过度表达NK-1R,这种联合疗法是治疗各类癌症的一种有前景的方法。鉴于阿瑞匹坦显示出成为一种广谱抗肿瘤药物的潜力,将这种NK-1R拮抗剂重新用作抗肿瘤药物是有必要的。本综述还将概述有关阿瑞匹坦/放疗联合治疗的研究。本综述的目的是提供关于癌症化疗/放疗与NK-1R拮抗剂联合研究的最新情况。
这种联合策略一旦得到证实,可能会开启化疗和放疗的新时代,具有更高的抗肿瘤活性和更少的副作用。这种治疗策略可能会转化为癌症患者更高的治愈率、更好的生活质量和更少的后遗症。