## BACKGROUND. The relative amounts of Bcl-2 and Bax proteins determine cell survival or death following an apoptotic stimulus. To clarify the molecular mechanism of cell death after radiotherapy or thermoradiotherapy and its relation to the response of AJCC/UICC Stage IIIB cervical carcinomas, the
Bax protein expression correlates with radiation-induced apoptosis in radiation therapy for cervical carcinoma
โ Scribed by Tatsuya Ohno; Takashi Nakano; Yuzuru Niibe; Hirohiko Tsujii; Kuniyuki Oka
- Publisher
- John Wiley and Sons
- Year
- 1998
- Tongue
- English
- Weight
- 300 KB
- Volume
- 83
- Category
- Article
- ISSN
- 0008-543X
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โฆ Synopsis
BACKGROUND.
Bax protein serves as a positive regulator of apoptosis by forming heterodimers with bcl-2 protein, thereby promoting cell survival. It is unclear whether the regulation of apoptosis reported in many studies is applicable to the apoptotic phenomenon observed in conventional fractionated radiation therapy for cervical carcinoma.
METHODS. The authors assessed the relation between apoptosis and the expression
of Bax and bcl-2 protein in fractionated radiation therapy for cervical carcinoma by using in situ nick end labeling (ISEL) and immunohistochemical methods.
RESULTS.
Specimens were excised from the cervical tumors of 20 patients before and after administration of a total irradiation dose of 9 gray (Gy). The apoptotic cell index (AI) in tumor cells was 0.22% before irradiation and 1.20% after the administration of the 9 Gy, which represented a significant increase (P ฯญ 0.0004). The positive rate of Bax protein increased from 15% (in 3 of 20 patients) before irradiation to 60% (in 12 of 20 patients) after the 9 Gy was administered, a statistically significant change (P ฯญ 0.0126). In addition, there was a significant correlation between Bax protein expression and apoptosis positivity after the 9 Gy was administered (P ฯญ 0.018).
CONCLUSIONS.
These results suggest that Bax protein is associated with apoptosis induced by fractionated radiation therapy.
๐ SIMILAR VOLUMES
patients treated with radiation therapy. Prognosis was analyzed by CerbB-OPE, growth fraction determined with Ki-67 immunohistochemistry (Ki-GF), and the Division of Radiation Medicine, National Instimitotic index of proliferating cell population (pMI). tute of Radiological Sciences, Chiba, Japan.