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Target for radiation-induced division delay

Journal Article · · Radiat. Res.; (United States)
DOI:https://doi.org/10.2307/3575485· OSTI ID:6984334
 [1];
  1. Thomas Jefferson Univ. Hospital, Philadelphia, PA
In an effort to elucidate the subcellular target responsible for radiation-induced division delay, Chinese hamster ovary (CHO) cells growing in monolayer cultures were pulse-labeled with /sup 125/IUdR and the cell kinetics monitored by counting the mitotic cells selected every 10 min. Our results showed that /sup 125/I had to be incorporated into DNA to cause a perturbation of cell progression; unlabeled G/sub 2/ cells were unperturbed. To evaluate the mechanism of /sup 125/I-induced division delay, /sup 125/IUdR-labeled cells were permitted to accumulate /sup 125/I decays either during the S phase or during both S and G/sub 2/ phases. The results indicated that cells which accumulated /sup 125/I decays only during the S phase did not experience enhanced delay. In contrast, the yield of mitotic cells was reduced in cells which accumulated /sup 125/I decays during S plus G/sub 2/. Analysis of the data suggests that the target for radiation-induced mitotic delay is not the DNA, but a cell structure which comes in contact with the DNA during G/sub 2/ or early M phase.
OSTI ID:
6984334
Journal Information:
Radiat. Res.; (United States), Journal Name: Radiat. Res.; (United States) Vol. 84:3; ISSN RAREA
Country of Publication:
United States
Language:
English

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