PO.ET02.08 · 实验与分子治疗
辣椒素纳米颗粒在人类NSCLC中表现出强效的生长抑制活性
Capsaicin nanoparticles display robust growth-inhibitory activity in human NSCLC
作者与单位 Authors & Affiliations
摘要 Abstract
中文摘要
目的:膳食化合物辣椒素(Capsaicin)是辣椒中辛辣刺激的成分。我们实验室的初步数据发现,辣椒素在人类肺癌中表现出强效的生长抑制活性。然而,辣椒素作为可行的抗癌药物的临床应用受到其不良副作用的阻碍,例如胃部刺激、恶心、胃痉挛以及肠道灼烧感。探索辣椒素镇痛活性的临床试验发现,口服辣椒素的患者因其令人不适的副作用而停止用药。规避这一缺陷的一种策略是将辣椒素封装于长效制剂中(如聚合物纳米颗粒)。一旦辣椒素被包裹在这些聚合物纳米颗粒中,它便以极其缓慢的速率释放,因此不会在患者体内产生任何“灼热感”和不良副作用。
实验方法:辣椒素[聚(乳酸-羟基乙酸共聚物)]纳米颗粒(以下称为CAP-PLGA-NPs)由一家生物技术公司定制合成。这些纳米颗粒的理化性质由供应商提供。我们在一组人类NSCLC细胞系中测试了这些CAP-PLGA-NPs的促凋亡活性。我们还测定了这些CAP-PLGA-NPs对正常人类肺、肝和肾细胞生长的影响。我们还进行了软琼脂实验,以评估CAP-PLGA-NP抑制软琼脂上非贴壁依赖性生长的能力。最后,我们在移植了人类NSCLC肿瘤的SCID小鼠中测试了CAP-PLGA-NPs的抗肿瘤活性。
结果:CAP-PLGA-NP在人类NSCLC中表现出比辣椒素更强的促凋亡活性。CAP-PLGA-NP在软琼脂实验中抑制了集落形成。最有趣的是,CAP-PLGA-NP不影响正常人类肺、肝和肾细胞的生长。静脉给予CAP-PLGA-NPs降低了移植于SCID小鼠体内的人类NSCLC肿瘤的生长速率。
结论:长效辣椒素药物制剂,即CAP-PLGA-NP,可能成为人类NSCLC中一种有前景的营养基础药物。
支持或资助信息:本研究的资助由NIH R15-AREA基金(2R15CA161491-02和2R15CA161491-03)、Women's Health T3:3P20GM103434-23W1(PI:G Rankin博士)资助给PD和MAV,以及NIAID-AI151970基金资助给TEL。本研究部分由西弗吉尼亚IDeA生物医学研究卓越网络(WV-INBRE)基金(NIH基金P20GM103434;PI:G. Rankin博士)以及美国国立卫生研究院下属国立普通医学科学研究所资助(奖励编号P30GM122733)。
查看英文原文 English abstract
Purpose of the study : The dietary compound Capsaicin is the hot and pungent ingredient of chili peppers. Preliminary data in our laboratory have found that capsaicin displays robust growth-inhibitory activity in human lung cancers. However, the clinical applications of capsaicin as a viable anti-cancer drug are hindered by its adverse side effects, such as gastric irritation, nausea, stomach cramps and a burning sensation in the gut. Clinical trials which explored the pain-relieving activity of capsaicin found that patients who orally ingested capsaicin discontinued taking the drug due to its unpleasant side effects. One strategy to circumvent this drawback is to encapsulate capsaicin in long-acting formulations (like polymeric nanoparticles). Once capsaicin is entrapped in these polymeric nanoparticles, it is released at a very slow rate, so it does not produce any “heat-sensation” and adverse side effects in patients
Experimental procedures: Capsaicin [poly(lactic-co-glycolic acid)] nanoparticles (hereby called CAP-PLGA-NPs] were custom synthesized by a biotech company. The physicochemical properties of these nanoparticles were provided by the vendor. We tested the pro-apoptotic activity of these CAP-PLGA-NPs in a panel of human NSCLC cell lines. We also measured the impact of these CAP-PLGA-NPs on the growth of normal human lung, liver and kidney cells. We also performed soft agar assays to evaluate the ability of CAP-PLGA-NP to inhibit anchorage independent-growth on soft agar. Finally, we tested the anti-neoplastic activity of CAP-PLGA-NPs in SCID mice xenografted with human NSCLC tumors.
Results: The CAP-PLGA-NP displayed greater pro-apoptotic activity than capsaicin in human NSCLCs. CAP-PLGA-NP inhibited colony-formation in soft agar assays. Most interestingly, CAP-PLGA-NP did not impact the growth of normal human lung, liver and kidney cells. The intravenous administration of CAP-PLGA-NPs decreased the rate of human NSCLC tumors xenografted in SCID mice
Conclusions: The long-acting capsaicin drug formulation, namely CAP-PLGA-NP, may be a promising nutrition-based drug in human NSCLCs.
Support or Funding Information Funding for our study was supported by the NIH R15-AREA Grant (2R15CA161491-02 and 2R15CA161491-03), the Women's Health T3: 3P20GM103434-23W1 (PI: Dr. G Rankin) to PD and MAV and the NIAID-AI151970 grant to TEL. This study was supported in part by the West Virginia IDeA Network of Biomedical Research Excellence (WV-INBRE) grant (NIH grant P20GM103434; PI: Dr. G. Rankin), the National Institute of General Medical Sciences of the National Institutes of Health under the award number P30GM122733.
利益披露 Disclosure
K. J. Modi, None..
R. S. Light, None..
K. B. Conley, None..
S. L. Miles, None..
P. Dasgupta, None.