Clonal cell populations unresponsive to radiosensitization induced by telomerase inhibition

被引:2
|
作者
Ju, Yeun-Jin
Shin, Hyun-Jin
Park, Jeong-Eun
Juhn, Kyoung-Mi
Woo, Seon Rang
Kim, Hee-Young
Han, Young-Hoon
Hwang, Sang-Gu
Hong, Sung-Hee
Kang, Chang-Mo
Yoo, Young-Do [2 ]
Park, Won-Bong [3 ]
Cho, Myung-Haing [4 ]
Park, Gil Hong [5 ]
Lee, Kee-Ho [1 ]
机构
[1] Korea Inst Radiol & Med Sci, Dept Radiat Canc Res, Div Radiat Canc Res, Seoul 139706, South Korea
[2] Korea Univ, Coll Med, Grad Sch Med, Mol Cell Biol Lab, Seoul 136705, South Korea
[3] Seoul Womens Univ, Div Nat Sci, Seoul 139774, South Korea
[4] Seoul Natl Univ, Toxicol Lab, Coll Vet Med, Seoul, South Korea
[5] Korea Univ, Coll Med, Dept Biochem, Seoul 136705, South Korea
关键词
Telomere; Radiosensitization; Chromosomal end-to-end fusion; Telomere length; IONIZING-RADIATION; P53; LENGTH; DYSFUNCTION; ABNORMALITIES; SENESCENCE; ABSENCE;
D O I
10.1016/j.bbrc.2010.09.091
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A combination of a radiotherapeutic regimen with telomerase inhibition is valuable when tumor cells are to be sensitized to radiation. Here, we describe cell clones unresponsive to radiosensitization after telomere shortening. After extensive division of individual transformed clones of mTERC(-/-) cells, about 22% of clones were unresponsive to radiosensitization even though telomerase action was inhibited. The telomere lengths of unsensitized mTERC(-/-) clones were reduced, as were those of most sensitized clones. However, the unsensitized clones did not exhibit chromosomal end-to-end fusion to the extent noted in all sensitized clones. Thus, a defense mechanism preventing telomere erosion is operative even when telomeres become shorter under conditions of telomerase deficiency, and results in unresponsiveness to the radiosensitization generally mediated by telomere shortening. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:198 / 202
页数:5
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