Abstract

BackgroundIntracavitary irradiation plays a pivotal role in definitive radiotherapy for cervical cancer, and the Ir-192 high dose-rate remote afterloading system (HDR-RALS) is often used for this purpose. Under this condition, tumor tissues receive remarkably different absorption doses, with a steep gradient, depending on distance from the radiation source. To obtain temporo-spatial information regarding cell-cycle kinetics in cervical cancer following irradiation by Ir-192 HDR-RALS, we examined HeLa cells expressing the fluorescence ubiquitination-based cell cycle indicator (Fucci), which allowed us to visualize cell-cycle progression.MethodsHeLa-Fucci cells, which emit red and green fluorescence in G1 and S/G2/M phases, respectively, were grown on 35-mm dishes and irradiated by Ir-192 HDR-RALS under normoxic and hypoxic conditions. A 6 French (Fr) catheter was used as an applicator. A radiation dose of 6 Gy was prescribed at hypothetical treatment point A, located 20 mm from the radiation source. Changes in Fucci fluorescence after irradiation were visualized for cells from 5 to 20 mm from the Ir-192 source. Several indices, including first green phase duration after irradiation (FGPD), were measured by analysis of time-lapse images.ResultsCells located 5 to 20 mm from the Ir-192 source became green, reflecting arrest in G2, in a similar manner up to 12 h after irradiation; at more distant positions, however, cells were gradually released from the G2 arrest and became red. This could be explained by the observation that the FGPD was longer for cells closer to the radiation source. Detailed observation revealed that FGPD was significantly longer in cells irradiated in the green phase than in the red phase at positions closer to the Ir-192 source. Unexpectedly, the FGPD was significantly longer after irradiation under hypoxia than normoxia, due in large part to the elongation of FGPD in cells irradiated in the red phase.ConclusionUsing HeLa-Fucci cells, we obtained the first temporo-spatial information about cell-cycle kinetics following irradiation by Ir-192 HDR-RALS. Our findings suggest that the potentially surviving hypoxic cells, especially those arising from positions around point A, exhibit different cell-cycle kinetics from normoxic cells destined to be eradicated.Electronic supplementary materialThe online version of this article (doi:10.1186/s13014-016-0669-8) contains supplementary material, which is available to authorized users.

Highlights

  • Intracavitary irradiation plays a pivotal role in definitive radiotherapy for cervical cancer, and the Ir-192 high dose-rate remote afterloading system (HDR-RALS) is often used for this purpose

  • In our previous reports using HeLa-fluorescence ubiquitination-based cell cycle indicator (Fucci) cells, we showed that elongation of the first green phase duration after irradiation (FGPD) and subsequent appearance of red cells perfectly reflects the G2 arrest kinetics following Xirradiation [10, 11]

  • We succeeded for the first time in visualizing the cellcycle kinetics in cells located at different distances from an Ir-192 HDR-RALS

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Summary

Introduction

Intracavitary irradiation plays a pivotal role in definitive radiotherapy for cervical cancer, and the Ir-192 high dose-rate remote afterloading system (HDR-RALS) is often used for this purpose. Under this condition, tumor tissues receive remarkably different absorption doses, with a steep gradient, depending on distance from the radiation source. Intracavitary irradiation using a high dose-rate radiation source, such as Ir-192, has been applied in the form of a remote afterloading system (RALS) [2, 3]. We reasoned that radioresponses of tumor cells, including cell-cycle kinetics, following such an intracavitary irradiation should differ markedly depending on distance from the radiation source. Following DNA damage, cell-cycle progression stops at the G1/S and G2/M checkpoints [5]. Flow-cytometric analysis using DNA content as a marker has been used to detect radiation-induced G2 arrest [8]; because this method requires preparation of single cells and fixation, spatial information is lost, and temporal information must be obtained from different cell populations

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