Adhya Amit Kumar, Srinivasan Radhika, Patel Firuza D
Department of Pathology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Int J Gynecol Pathol. 2006 Jul;25(3):281-7. doi: 10.1097/01.pgp.0000215292.99996.44.
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.
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.
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.
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.
癌症放射治疗(RT)通过凋亡诱导细胞死亡。主要的凋亡调节分子包括Bcl-2、Bcl-XL(抗凋亡)和Bax(促凋亡)蛋白。宫颈浸润性鳞状细胞癌主要通过放疗进行治疗,因此我们的目的是评估放疗诱导的凋亡指数(AI)变化,并将其与主要促凋亡和抗凋亡分子的水平相关联。
对30例宫颈浸润癌患者在10 Gy放疗前后进行配对活检。采用TUNEL法检测凋亡细胞核,免疫组织化学(IHC)检测Bcl-2、Bcl-XL和Bax蛋白。使用Spearman等级相关系数检验进行统计分析。
放疗后,平均AI显著增加[放疗后为2.25(±2.28),放疗前组为0.90(±0.53)]。主要促凋亡蛋白Bax在放疗后显著增加(P < 0.05),而抗凋亡的Bcl-XL显著降低(P = 0.006)。Bcl-2表达无显著变化。两组中Bcl-2和Bax的IHC评分及Bcl-2/Bax比值与AI均无相关性。放疗前组Bcl-XL与AI呈负相关(P = 0.003),但放疗后组无此相关性。
宫颈浸润性鳞状细胞癌的放疗导致凋亡性细胞死亡增加,促凋亡蛋白Bax上调,抗凋亡蛋白Bcl-XL下调,而Bcl-2水平无任何显著变化。