Differentiation state of skin fibroblast cultures versus risk of subcutaneous fibrosis after radiotherapy

被引:52
作者
Herskind, C
Bentzen, SM
Overgaard, J
Overgaard, M
Bamberg, M
Rodemann, HP
机构
[1] Univ Tubingen, Dept Radiotherapy, Sect Radiobiol & Mol Environm Res, D-72076 Tubingen, Germany
[2] Aarhus Univ Hosp, Danish Canc Soc, Dept Expt Clin Oncol, DK-8000 Aarhus C, Denmark
[3] Aarhus Univ Hosp, Dept Oncol, DK-8000 Aarhus C, Denmark
关键词
differentiation; fibroblasts; fibrosis; normal tissue response; predictive test; radiotherapy;
D O I
10.1016/S0167-8140(98)00018-8
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background and purpose: There is increasing evidence for patient-to-patient variation in the response of normal tissue to radiotherapy. Recently, it has been suggested that accumulation of functional fibrocytes may be a key step in the development of radiation-induced fibrosis. Therefore, we have examined a possible relationship between the differentiation state of untreated fibroblasts and the risk of radiation-induced subcutaneous fibrosis in individual patients. Materials and methods: We used skin fibroblast cultures isolated from eight postmastectomy radiotherapy patients whose individual clinical radiosensitivity was assessed by the mean excess risk of fibrosis. Different types of potentially mitotic progenitor fibroblasts (MF) and postmitotic functional fibrocytes (PMF) in the terminal differentiation lineage, MFI --> MFII --> MFIII --> PMF, were scored morphologically in clonal culture. Progression of differentiation was quantified by the ratio L/E of colony-forming late (MFIII and late MFII) and early (MFI and early MFII) progenitors. Results: We observed a correlation between the ratio L/E and the mean risk of fibrosis (r(s) = 0.743, P = 0.03), indicating an approximately 10-fold increase in L/E with an increasing risk of fibrosis. This was paralleled by a decreasing trend in the absolute numbers of early progenitor types. By contrast, there was no significant correlation between the plating efficiency and the risk of fibrosis. Conclusions: The data suggest that the risk of fibrosis increases with the progression of the differentiation of untreated progenitor fibroblasts, indicating that the progression of fibroblast differentiation may be a co-factor in the development of radiation-induced fibrosis. Lf this hypothesis is validated, it provides a rationale for a novel predictive rest to identify patients with an increased risk of subcutaneous fibrosis. (C) 1998 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:263 / 269
页数:7
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