Radiation therapy induced changes in apoptosis and its major regulatory proteins, Bcl-2, Bcl-XL, and Bax, in locally advanced invasive squamous cell carcinoma of the cervix

被引:41
作者
Adhya, Amit Kumar
Srinivasan, Radhika [1 ]
Patel, Firuza D.
机构
[1] Postgrad Inst Med Educ & Res, Dept Cytol & Gynecol Pathol, Chandigarh 160012, India
[2] Postgrad Inst Med Educ & Res, Dept Pathol, Chandigarh 160012, India
[3] Postgrad Inst Med Educ & Res, Dept Radiotherapy, Chandigarh 160012, India
关键词
Bcl-2; Bcl-XL; Bax; carcinoma cervix; radiotherapy;
D O I
10.1097/01.pgp.0000215292.99996.44
中图分类号
R71 [妇产科学];
学科分类号
100211 [妇产科学];
摘要
Background and Purpose: Radiation therapy (RT) for cancer induces cell death by apoptosis. The major apoptotic regulatory molecules include Bcl-2, Bcl-XL (antiapoptotic), and Bax,(proapoptotic) proteins. Invasive squamous cell carcinoma of the cervix is mainly treated by radiation, and hence our aim was to evaluate the changes induced by RT in the apoptotic index (AI) and to correlate this to the levels of the major pro- and antiapoptotic molecules. Materials and Methods: Paired biopsies were obtained in 30 cases of invasive carcinoma cervix before and after 10 Gy RT. The TUNEL assay was performed to detect apoptotic nuclei and Bcl-2, Bcl-XL, and Bax proteins detected by immunohistochemistry (IHC). Statistical analysis was performed using the Spearman rank correlation coefficient test. Results: Following RT, there was a significant increase in the mean AI [2.25 ( +/- 2.28) in post-RT vs 0.90 (+0.53) in the pre-RT group]. Bax, a major proapoptotic protein, was significantly increased following RT (p < 0.05), whereas the antiapoptotic Bcl-XL showed a significant decrease (p = 0.006). There was no significant change in Bcl-2 expression. The Bcl-2 and Bax IHC scores and the Bcl-2/Bax ratio did not correlate with AI in the 2 groups. There was an inverse correlation of Bcl-XL to AI in the pre-RT group (p = 0.003) but not in the post-RT group. Conclusions: RT for invasive squamous cell carcinoma of cervix results in increased apoptotic cell death with the up-regulation of Bax, a proapoptotic protein, and the down-regulation of Bcl-XL, an antiapoptotic protein, without any significant change in the levels of Bcl-2.
引用
收藏
页码:281 / 287
页数:7
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