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Editorial Hot Topic: Applications of the Photodynamic Therapy to Cancer,Water- and Vector-Borne Diseases (Guest Editor: Luigi E. Xodo )

机译:社论热门话题:光动力疗法在癌症,水传染和媒介传染病中的应用(来宾编辑:Luigi E. Xodo)

摘要

Applications of the Photodynamic Therapy to Cancer, Water- and Vector-Borne DiseasesPhotodynamic therapy (PDT) is a clinically approved treatment modality for various types of diseases, including cancer, that produces a selective cytotoxic effect on the target cells. It involves the use of a photosensitizing molecule and a source of light with a wavelength that corresponds to the absorption band of the photosensitizer. After photoactivation, the photosensitizer occupies an excited triplet state from which it transfers its energy to neighboring oxygen molecules, thus generating singlet oxygen and reactive oxygen species (“oxidative stress”) which lead to cell death mediated by apoptosis and/or necrosis. PDT is less invasive than conventional chemotherapy, as the photosensitizer is not cytotoxic in the dark and the photoprocess is confined to the diseased tissue irradiated by light. In addition to the treatment of cancer and precancerous conditions, the use of PDT to cure microbial localized infections and inactivate pathogens is rapidly expanding.This special issue will address (i) the application of nanotechnology to PDT for improving the delivery of photosensitizers to the diseased tissue; (ii) the molecular response of cancer cells to the naturally-occurring photosensitizer hypericin; (iii) the photosensitizing properties of pheophorbide, a chlorophyll derivative, as a free or conjugated molecule; (iv) applications of PDT to water- and vector-borne diseases.Most of the clinically used photosensitizers are scarcely soluble in aqueous media, they do not accumulate efficiently in tumor tissues and often show an undesired liver accumulation. In an effort to overcome these shortcomings, research work has recently been directed to the development of nanoparticle-based photosensitizers. The contribution of Frochot and co-workers summarizes the use of nanoparticles (NPs) to enhance the delivery of scarcely soluble photosensitizers. NP technology offers a variety of advantages that are discussed in this review, including the transport of hydrophobic drugs in the blood, the possibility to decorate the NP surface with specific molecules in order to improve both uptake and tumor selectivity, the capacity of NPs to deliver a high “payload” in the diseased tissue and, in certain cases, the possibility to excite directly NPs to generate oxidative stress. The review describes the chemical nature of NPs and the recent advances in the area of non-polymeric nanoparticles. A comprehensive presentation of gold and silica nanoparticles, carbon nanotubes, TiO2/ZnO and magnetic nanoparticles is provided.Krammer and Verwanger focus their review on the molecular response of cancer cells to PDT. The authors provide a thorough analysis of the cellular response to hypericin-induced photodamage and describe how the hypericin-PDT dose can dictate cell growth or cell death. Low doses stimulate cell growth via the p38 or JNK survival pathways, whereas high doses favor apoptosis or autophagic cell death, depending on the availability of Bax/Bak. The different modes of cellular responses correlate with the PDT-protocol, photosensitizer localization, cell damage protection and available intracellular energy. This review provides useful information for the design of new protocols aiming to reduce cell recurrence in PDT.Xodo and coworkers provide an update of the studies carried out with pheophorbide a (Pba), a derivative of chlorophyll a which shows a high PDT potential but has not yet been used in clinic. Their review refers to the basic reports describing the photophysical properties of Pba, its capacity to induce apoptosis in cancer cells, its pharmacokinetics and its in vivo efficacy against primary tumor growth. The authors discuss the efficiency in vivo of Pba conjugated to carrier polymers such as polyethylene glycol or peptide molecules. They also report that Pba is a generator of nitric oxide (NO) and that low intracellular NO levels (low dose Pba-PDT) seem to be responsible for cell recurrence through activation of NF-kB/anti-apoptotic Snail and repression of pro-apoptotic RKIP. In contrast, high NO levels (high dose Pba-PDT) repress NF-kB/Snail and activate pro-apoptotic RKIP. Finally, the review discusses the correlation between PDT and the NF-kB/Snail/RPIK loop, in the perspective of developing novel strategies to reduce cellular rescue in tissue regions which receive a low dose PDT.The last review, by Coppellotti and co-workers, reports on porphyrin/phthalocyanines/chlorines photosensitized processes in the prevention and treatment of water- and vector-borne diseases. The spreading of epidemic diseases due to the diffusion of antibiotic-resistant microbial strains makes PDT an attractive alternative to most of the presently employed therapeutic modalities. The field of antimicrobial PDT is rapidly growing, as suggested by the identification of novel photosensitizing agents with a high selectivity for microbial cell targeting. The application of PDT to water disinfection appears particularly attractive, as it can be achieved by the concerted action of sunlight and photosensitizers of natural origin that guarantee a minimal impact on the environment. The review outlines the principal antimicrobial photodynamic approaches which have been so far proposed to inactivate a large variety of pathogens causing water-borne diseases (bacteria, protozoa, fungi and metazoa) and the vectors (protozoa and arthropods) responsible for vector–borne diseases.I hope this special issue will be beneficial to researchers working in the field of photodynamic therapy. It is important to acknowledge that this issue focuses on only a small part of what is known about PDT. More exhaustive reviews on PDT have been published in the last few years.
机译:光动力疗法在癌症,水和媒介传染病中的应用光动力疗法(PDT)是经临床认可的多种治疗方法,可治疗多种类型的疾病,包括癌症,对靶细胞产生选择性的细胞毒性作用。它涉及光敏分子和波长与光敏剂吸收带相对应的光源的使用。在光活化之后,光敏剂处于激发的三重态,从中将其能量转移到相邻的氧分子,从而产生单重态氧和活性氧(“氧化应激”),导致细胞凋亡和/或坏死介导的细胞死亡。由于光敏剂在黑暗中不具有细胞毒性,并且光过程仅限于光照射的患病组织,因此PDT的侵袭性不如常规化学疗法。除了治疗癌症和癌前疾病外,PDT在治疗微生物局部感染和灭活病原体方面的应用正在迅速扩大。这一特殊问题将解决(i)纳米技术在PDT中的应用,以改善对疾病患者的光敏剂的递送。组织; (ii)癌细胞对自然发生的光敏剂金丝桃素的分子反应; (iii)脱镁叶绿素(ophophorbide)(一种叶绿素衍生物)作为游离或共轭分子的光敏特性; (iv)PDT在水传播和媒介传播疾病中的应用大多数临床上使用的光敏剂几乎不溶于水介质,它们在肿瘤组织中不能有效地积累,并且经常表现出不希望的肝脏积累。为了克服这些缺点,最近的研究工作针对基于纳米粒子的光敏剂的开发。 Frochot及其同事的贡献总结了使用纳米颗粒(NPs)来增强难溶光敏剂的递送。 NP技术具有本综述中讨论的多种优势,包括血液中疏水性药物的运输,用特定分子修饰NP表面以改善摄取和肿瘤选择性的可能性,NP传递的能力患病组织的“有效载荷”很高,在某些情况下,还可能直接激发NP产生氧化应激。这篇综述描述了NP的化学性质以及非聚合纳米颗粒领域的最新进展。提供了金和二氧化硅纳米颗粒,碳纳米管,TiO2 / ZnO和磁性纳米颗粒的全面介绍。Krammer和Verwanger着重研究了癌细胞对PDT的分子反应。作者全面分析了细胞对金丝桃素诱导的光损伤的反应,并描述了金丝桃素-PDT剂量如何决定细胞生长或细胞死亡。低剂量通过p38或JNK存活途径刺激细胞生长,而高剂量则有利于凋亡或自噬细胞死亡,具体取决于Bax / Bak的可用性。细胞反应的不同模式与PDT协议,光敏剂定位,细胞损伤保护和可用细胞内能量相关。这篇综述为旨在减少PDT中细胞复发的新方案的设计提供了有用的信息.Xodo及其同事提供了对脱镁叶绿素a(Pba)的研究的最新进展,该叶绿素a的衍生物具有较高的PDT潜力,但具有尚未在临床中使用。他们的综述参考了描述Pba的光物理特性,其在癌细胞中诱导凋亡的能力,药代动力学及其对原发性肿瘤生长的体内功效的基本报道。作者讨论了与载体聚合物(例如聚乙二醇或肽分子)偶联的Pba在体内的效率。他们还报告说Pba是一氧化氮(NO)的产生者,而低细胞内NO水平(低剂量Pba-PDT)似乎是通过激活NF-kB /抗凋亡Snail和抑制促性腺激素导致细胞复发的原因。凋亡性RKIP。相反,高NO水平(高剂量Pba-PDT)会抑制NF-kB / Snail并激活促凋亡的RKIP。最后,本综述从开发新的策略以减少接受低剂量PDT的组织区域的细胞拯救的角度探讨了PDT与NF-kB / Snail / RPIK环之间的相关性。最后一篇综述,由Coppellotti和co-工人,有关卟啉/酞菁/氯的光敏化过程在预防和治疗水媒传染病中的报道。由于抗生素抗性微生物菌株的扩散,流行病的传播使PDT成为目前大多数采用的治疗方法的有吸引力的替代方法。抗菌PDT领域正在迅速发展如通过鉴定对微生物细胞靶向具有高选择性的新型光敏剂所建议的。 PDT在水消毒中的应用似乎特别有吸引力,因为它可以通过阳光和天然光敏剂的协同作用来实现,从而确保对环境的影响最小。综述概述了迄今为止已提出的主要的抗菌光动力学方法,该方法可以灭活引起水传播疾病(细菌,原生动物,真菌和后生动物)的多种病原体以及引起媒介传播疾病的媒介(原生动物和节肢动物)。我希望这个特刊对光动力疗法领域的研究人员有所帮助。重要的是要承认,这个问题只集中在有关PDT的一小部分。过去几年中,已经发布了有关PDT的更详尽的评论。

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    Luigi E. Xodo;

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  • 年度 2012
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  • 原文格式 PDF
  • 正文语种 eng
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