Radiosensitivity of human normal and tumoral thyroid cells using fluorescence in situ hybridization and clonogenic survival assay

Citation
A. Gaussen et al., Radiosensitivity of human normal and tumoral thyroid cells using fluorescence in situ hybridization and clonogenic survival assay, INT J RAD O, 44(3), 1999, pp. 683-691
Citations number
48
Categorie Soggetti
Radiology ,Nuclear Medicine & Imaging","Onconogenesis & Cancer Research
Journal title
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS
ISSN journal
03603016 → ACNP
Volume
44
Issue
3
Year of publication
1999
Pages
683 - 691
Database
ISI
SICI code
0360-3016(19990601)44:3<683:ROHNAT>2.0.ZU;2-K
Abstract
Purpose: By using cell survival as a reference, we evaluated the radiosensi tivity of human normal and tumoral thyroid cells using of radiation-induced translocations. Methods and Materials: Tissue samples were obtained from patients undergoin g thyroidectomy, Cell cultures were established, irradiated with Co-60, and metaphases painted using commercial whole-chromosome 4 hybridization probe and pancentromeric probe. The clonogenic survival was assessed by conventi onal colony forming assay. Results: After irradiation, normal cultured thyroid cells yielded a higher number of translocations than cultures derived from adenomas or thyroid car cinoma. The colony forming assay demonstrated, by way of the mean inactivat ion dose, a higher survival of thyroid carcinoma and adenoma cells than of normal thyroid cells. This difference between tumoral and nontumoral cells is significant in each method (p = 0.0001), and cannot be explained by apop tosis in irradiated malignant cells. Correlation of the results obtained by both methods is shown by comparing the survival fraction at 2 Gy (SF2) and the percentage of chromosome 4 translocations at 2 Gy. Conclusion: These results indicate that the yield of radiation-induced tran slocations serves as a good and rapid prediction of the intrinsic radiosens itivity of thyroid cells, and that this test could be applied to other tumo rs, (C) 1999 Elsevier Science Inc.