Peng Qian, Nesland Jahn M
Department of Pathology, The Norwegian Radium Hospital, University of Oslo, Oslo, Norway.
Ultrastruct Pathol. 2004 Sep-Dec;28(5-6):333-40. doi: 10.1080/01913120490515586.
Photodynamic therapy (PDT) is a treatment that combines a photosensitizer with light to generate oxygen-dependent photochemical destruction of diseased tissue. This modality has been approved worldwide since 1993 for the treatment of several oncological and nononcological disorders. PDT continues to be interested in both preclinical and clinical research, with more than 500 publications each year during the past 5 years. This minireview focuses on the effects of PDT on tumor stroma. A tumor consists of two fundamental elements: parenchyma (neoplastic cells) and stroma. The stroma is composed of vasculature, cellular components, and intercellular matrix and is necessary for tumor growth. All the stromal components can be targeted by PDT. Although the exact mechanism of PDT is unknown, emerging evidence has indicated that effective PDT of tumor requires destruction of both parenchyma and stroma. Further, damage to subendothelial zone of vasculature, in addition to endothelium, also appears to be a crucial factor. The PDT-generated immune response as a way of vaccination for treatment and prevention of metastatic tumors remains to be exploited.
光动力疗法(PDT)是一种将光敏剂与光相结合,对病变组织进行氧依赖性光化学破坏的治疗方法。自1993年以来,这种治疗方式已在全球范围内被批准用于治疗多种肿瘤和非肿瘤疾病。PDT在临床前和临床研究中一直备受关注,在过去5年中,每年有超过500篇相关出版物。这篇微型综述聚焦于PDT对肿瘤基质的影响。肿瘤由两个基本要素组成:实质(肿瘤细胞)和基质。基质由脉管系统、细胞成分和细胞间基质组成,是肿瘤生长所必需的。所有基质成分都可被PDT靶向作用。尽管PDT的确切机制尚不清楚,但新出现的证据表明,有效的肿瘤PDT需要同时破坏实质和基质。此外,除了内皮细胞外,脉管系统内皮下区域的损伤似乎也是一个关键因素。作为治疗和预防转移性肿瘤的一种疫苗接种方式,PDT所引发的免疫反应仍有待开发利用。