Dörr W
Klinik und Poliklinik für Strahlentherapie und Radioonkologie, Medizinische Fakultät Carl Gustav Carus, Technische Universität Dresden.
Strahlenther Onkol. 1998 Nov;174 Suppl 3:4-7.
The present review summarizes radiobiological models of normal tissue responses to radiation and their consequences for potential therapeutic interventions.
Common radiobiological principles and pathogenetic models can be established for classes of tissues. These models may support the development of general modalities, both therapeutic and supportive, for the modulation of these responses.
The stem cell concept, based on studies in standard tissue culture, describes the clonogenic survival after radiation treatment. The factors affecting cell survival are summarized as the 4 Rs of radiotherapy. Based on the stem cell concept, the reactions of normal tissue to ionising radiation were considered a consequence exclusively of the proliferative sterilisation of cells of a given target cell population. Once stem cells are inactivated, responses develop in a passive manner. However, recent studies into the pathogenesis of radiation tissue injury have clearly shown that numerous postirradiation events occur during the symptom-free latent time in irradiated cells and tissues, which modulate the manifestation of damage. These are summarized by models of tissue radiation pathology.
Cellular radiobiology and the tissue models based on the stem cell concept assume that exclusively the sterilisation of target cells is the radiation effect which results in both acute and late tissue responses. As a consequence, the radiation sensitivity can only be modulated by modification of radiobiological parameters at the time of irradiation, while at later time points only symptomatic treatment can be applied. Tissue radiation pathology, in contrast, allows for post-irradiation modification of the manifestation of radiation sequelae in tissues.
本综述总结了正常组织对辐射反应的放射生物学模型及其对潜在治疗干预的影响。
可为各类组织建立常见的放射生物学原理和发病机制模型。这些模型可能支持开发用于调节这些反应的通用治疗和支持方式。
基于标准组织培养研究的干细胞概念描述了放射治疗后的克隆源性存活。影响细胞存活的因素总结为放射治疗的4R。基于干细胞概念,正常组织对电离辐射的反应被认为完全是给定靶细胞群体细胞增殖性失活的结果。一旦干细胞失活,反应就以被动方式发展。然而,最近对辐射组织损伤发病机制的研究清楚地表明,在受照射细胞和组织的无症状潜伏期内会发生许多照射后事件,这些事件会调节损伤的表现。这些由组织辐射病理学模型进行总结。
细胞放射生物学和基于干细胞概念的组织模型假定,只有靶细胞的失活是导致急性和晚期组织反应的辐射效应。因此,辐射敏感性只能在照射时通过改变放射生物学参数来调节,而在后期只能进行对症治疗。相比之下,组织辐射病理学允许对组织中辐射后遗症的表现进行照射后修饰。