Combination Therapy of Chemotherapy or Radiotherapy and the Neurokinin-1 Receptor Antagonist Aprepitant: A New Antitumor Strategy?

消炎药 化疗 医学 NK1受体拮抗剂 放射治疗 药理学 速激肽受体1 癌症 联合疗法 副作用(计算机科学) 肿瘤科 P物质 内科学 受体 止吐药 神经肽 程序设计语言 计算机科学
作者
Prema Robinson,Rafael Coveñas,Miguel Muñoz
出处
期刊:Current Medicinal Chemistry [Bentham Science]
卷期号:30 (16): 1798-1812 被引量:13
标识
DOI:10.2174/0929867329666220811152602
摘要

Background: 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. Objective: 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. Conclusion: 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.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
更新
大幅提高文件上传限制,最高150M (2024-4-1)

科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
1秒前
xxx关注了科研通微信公众号
1秒前
现实的向梦完成签到 ,获得积分10
2秒前
闪闪的鹏博完成签到,获得积分10
2秒前
嵇冷雪完成签到,获得积分10
3秒前
雯雯子完成签到,获得积分10
4秒前
咱不吃葱完成签到,获得积分10
5秒前
7秒前
雯雯子发布了新的文献求助10
8秒前
赘婿应助谦让的小姜采纳,获得10
8秒前
大个应助木子niko采纳,获得10
8秒前
LIKO发布了新的文献求助20
11秒前
11秒前
咚咚完成签到,获得积分10
12秒前
12秒前
小马甲应助科研通管家采纳,获得10
12秒前
12秒前
12秒前
赘婿应助ZY采纳,获得10
12秒前
田様应助科研通管家采纳,获得10
12秒前
大模型应助科研通管家采纳,获得10
12秒前
浅尝离白应助科研通管家采纳,获得30
12秒前
Hello应助科研通管家采纳,获得30
12秒前
科研通AI2S应助科研通管家采纳,获得10
12秒前
隐形曼青应助科研通管家采纳,获得10
12秒前
丘比特应助科研通管家采纳,获得10
13秒前
科研通AI2S应助科研通管家采纳,获得10
13秒前
彭于晏应助科研通管家采纳,获得10
13秒前
今后应助科研通管家采纳,获得10
13秒前
在水一方应助科研通管家采纳,获得10
13秒前
浅尝离白应助科研通管家采纳,获得30
13秒前
无花果应助科研通管家采纳,获得10
13秒前
13秒前
13秒前
李健应助科研通管家采纳,获得10
13秒前
华仔应助科研通管家采纳,获得10
13秒前
打打应助科研通管家采纳,获得30
13秒前
今后应助科研通管家采纳,获得10
13秒前
Orange应助科研通管家采纳,获得30
13秒前
科研通AI2S应助科研通管家采纳,获得10
13秒前
高分求助中
Kinetics of the Esterification Between 2-[(4-hydroxybutoxy)carbonyl] Benzoic Acid with 1,4-Butanediol: Tetrabutyl Orthotitanate as Catalyst 1000
The Young builders of New china : the visit of the delegation of the WFDY to the Chinese People's Republic 1000
Rechtsphilosophie 1000
Bayesian Models of Cognition:Reverse Engineering the Mind 888
Very-high-order BVD Schemes Using β-variable THINC Method 568
Chen Hansheng: China’s Last Romantic Revolutionary 500
XAFS for Everyone 500
热门求助领域 (近24小时)
化学 医学 生物 材料科学 工程类 有机化学 生物化学 物理 内科学 纳米技术 计算机科学 化学工程 复合材料 基因 遗传学 催化作用 物理化学 免疫学 量子力学 细胞生物学
热门帖子
关注 科研通微信公众号,转发送积分 3138252
求助须知:如何正确求助?哪些是违规求助? 2789208
关于积分的说明 7790538
捐赠科研通 2445551
什么是DOI,文献DOI怎么找? 1300565
科研通“疑难数据库(出版商)”最低求助积分说明 625925
版权声明 601053