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MTA1、nm23H1 mRNA表达及突变与卵巢癌淋巴结转移的关系
引用本文:黄光琦,宋毅,贺国丽. MTA1、nm23H1 mRNA表达及突变与卵巢癌淋巴结转移的关系[J]. 中华肿瘤杂志, 2001, 23(1): 31-34
作者姓名:黄光琦  宋毅  贺国丽
作者单位:1. 华西医科大学附属第一医院肿瘤研究所
2. 海南省人民医院妇产科
摘    要:目的 研究MAT1、nm23H1 mRNA表达及突变与卵巢癌淋巴结转移的关系。方法 应用逆转录-PCR(RT-PCR)和逆转录-PCR-单链构像多态性分析(RT-PCR-SSCP)技术,对8例正常卵巢、20例卵巢癌及其相应的20例淋巴结组织,进行MTA1和nm23H1 mRNA表达及突变的检测。结果 转移卵巢癌原发灶MTA1 mRNA高表达率为100%(7/7),无转移为38.5%(5/13),P=0.0103;有癌转移淋巴结高表达率为87.5%(6/7),无癌转移为23%(3/13),P=0.0043;有癌转移淋巴结低表达率为100%(7/7),无癌转移为38.5%(5/13),P=0.0102。MTA1/nm23H1 mRNA表达的相对吸光度值(A值,曾称光密度OD值)的比值随转移而增加。单链构像多态性分析(SSCP)未发现突变。结论 MTA1、nm23H1基因的转录表达与卵巢癌淋巴结转移呈正负相关关系,起着下负调控的重要作用。这两个基因的异常表达是卵巢癌转移中的频发事件而与基因突变无关。

关 键 词:卵巢癌 淋巴结转移 MTA1基因 nm23H1基因 mRNA表
修稿时间:1999-11-24

mRNA expression and mutation of MTA1 and nm23H1 genes in ovarian carcinoma in relation to lymph node metastasis
HUANG Guangqi,SONG Yi,HE Guoli. mRNA expression and mutation of MTA1 and nm23H1 genes in ovarian carcinoma in relation to lymph node metastasis[J]. Chinese Journal of Oncology, 2001, 23(1): 31-34
Authors:HUANG Guangqi  SONG Yi  HE Guoli
Affiliation:Institute of Cancer Research, First Affiliated Hospital, West China University of Medical Sciences, Chengdu 610041, China.
Abstract:OBJECTIVE: To investigate mRNA expression and mutation of MTA1 and nm23H1 genes in ovarian carcinoma (OC) in relation to lymph node (LN) metastasis. METHODS: A panel of eight normal ovarian tissues, twenty primary OC specimens and twenty corresponding LNs was examined for mRNA expression and mutation of MTA1 and nm23H1 genes by using RT-PCR and RT-PCR-SSCP. The level of expression was determined by the relative optic density (ROD) of the PCR products. RESULTS: The frequency of MTA1 overexpression was 100% (7/7) in primary OC with metastasis but only 38.5% (5/13) in those without metastasis (P = 0.0103). Overexpression of MTA1 was observed in 87.5% (6/7) of LNs with metastasis but in only 23% (3/13) of LNs without metastasis (P = 0.0118). In contrast with MTA1, low expression of nm23H1 mRNA was seen in 7 of 7 OC with metastasis but only in 4 of 13 (30%) of those without metastasis (P = 0.0043). Low nm23H1 expression was also seen in 7 of 7 LNs with metastasis but only in 5 of 13 (38.5%) nonmetastatic LNs (P = 0.0102). The ROD ratio of MTA1 to nm23H1 increased with the development of metastasis. No mutation of MTA1 and nm23H1 was found by SSCP analysis. CONCLUSION: The mRNA expression of MTA1 and nm23H1 is positively and negatively correlated with LN metastasis, respectively. Expression abnormalities but not mutation of the two genes are frequent events related to LN metastasis of ovarian cancer.
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