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作 者:杨宝龙[1] 顾方六[1] 王行环[1] 邓方明[1] 孔祥田[1]
机构地区:[1]北京医科大学泌尿外科研究所
出 处:《中华外科杂志》1997年第10期602-604,共3页Chinese Journal of Surgery
摘 要:为探讨凋亡抑制基因bcl-2和凋亡促进基因bax表达产物在膀胱癌组织中的分布及意义,作者应用抗bcl-2单克隆抗体和抗bax多克隆抗体分别对34例膀胱癌和9例正常膀胱粘膜组织的石蜡切片进行免疫组化染色。结果显示,9例正常膀胱粘膜有4例bcl-2蛋白表达阳性(44.44%),34例膀胱癌有28例bcl-2蛋白表达阳性(82.35%),两组间差异有显著意义(P<0.05),随肿瘤分级的增加,阳性表达增强。9例正常膀胱粘膜有8例bax蛋白表达阳性(88.89%),34例膀胱癌有18例表达阳性(52.94%),两组间差异有显著意义(P<0.05)。作者认为,bcl-2和bax蛋白在膀胱癌组织中的异常表达,参与了膀胱癌的发生及进展过程。To investigate the role of bcl 2(an apoptosis suppressing oncogene) and bax(an apoptosis accelerating oncogene) in the development of TCC.We investigated bcl 2 and bax expression by means of immunohistochemical technique in 34 cases of TCC and in 9 cases of normal bladder tissue. Bcl 2 was positive in 44 44% of normal bladder tissue and in 82 35% of TCC. Bcl 2 staining intensity was significantly stronger in TCC than that in normal bladder tissue. Intensity and positivity of bcl 2 also increased with increasing grades of TCC. Bax was positive in 88 89% of normal bladder tissue and in 52 94% of TCC. Bax staining intensity was significantly weaker in TCC than that in the normal bladder tissue. These results suggested that increased expression of bcl 2 and decreased expression of bax in TCC play an important role in the development of TCC.
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