McMenamin M E, O'Neill A J, Gaffney E F
Department of Histopathology, St James's Hospital, Dublin, Ireland.
Mol Pathol. 1997 Oct;50(5):242-6. doi: 10.1136/mp.50.5.242.
To assess the extent of apoptosis in ovarian serous carcinoma and to examine possible relations between apoptosis, cell proliferation, p53 overexpression, and patient survival.
Apoptotic and mitotic indices were obtained by examining haematoxylin and eosin stained sections from 30 patients with ovarian serous carcinoma. Apoptosis was also evaluated semiquantitatively by in situ end labelling of fragmented DNA. Expression of p53 and determination of Ki-67 labelling indices were based on immunohistochemical staining. Clinical details were obtained from patients' clinical records. For statistical analysis, Fisher's exact test, parametric (Pearson) linear correlations, and the Kaplan-Meier method were used.
The mean apoptotic index was 1.3% (range 0.02-3.9%), the mean mitotic index was 0.4% (range 0.02-1.1%), and the mean Ki-67 labelling index was 16% (range 4-32%). There were significant correlations between the apoptotic and mitotic indices (p < 0.0205) and between the mitotic and Ki-67 labelling indices (p < 0.024). There was a significant correlation between a high apoptotic index and poor prognosis (p < 0.02). p53 was overexpressed in 16 cases but the extent of apoptosis and outcome were both independent of p53 status.
These results suggest that regulation of apoptosis is an integral component of tumour cell kinetics in ovarian serous carcinoma, and that increased apoptosis is indicative of aggressive tumour growth. p53 expression did not correlate with altered apoptosis, but the possibility of an attenuated apoptotic response to subsequent DNA damage by anticancer agents is not excluded.
评估卵巢浆液性癌中的细胞凋亡程度,并研究细胞凋亡、细胞增殖、p53过表达与患者生存率之间的可能关系。
通过检查30例卵巢浆液性癌患者苏木精-伊红染色切片获得凋亡指数和有丝分裂指数。还通过对断裂DNA进行原位末端标记对凋亡进行半定量评估。p53表达和Ki-67标记指数的测定基于免疫组织化学染色。临床细节从患者的临床记录中获取。统计分析采用Fisher精确检验、参数(Pearson)线性相关分析和Kaplan-Meier法。
平均凋亡指数为1.3%(范围0.02 - 3.9%),平均有丝分裂指数为0.4%(范围0.02 - 1.1%),平均Ki-67标记指数为16%(范围4 - 32%)。凋亡指数与有丝分裂指数之间存在显著相关性(p < 0.0205),有丝分裂指数与Ki-67标记指数之间也存在显著相关性(p < 0.024)。高凋亡指数与预后不良之间存在显著相关性(p < 0.02)。16例患者p53过表达,但凋亡程度和预后均与p53状态无关。
这些结果表明,细胞凋亡的调控是卵巢浆液性癌肿瘤细胞动力学的一个组成部分,凋亡增加表明肿瘤生长活跃。p53表达与凋亡改变无关,但不排除对抗癌药物后续DNA损伤的凋亡反应减弱的可能性。