摘要
为了解卵巢癌组织中抗癌基因p53与Rb基因的突变情况,我们把PCR单链构象多态(PCR-SSCP)银染技术及PCR-DNA直接测序方法应用于57例卵巢癌组织细胞的检测。结果发现p53基因可能的突变率为32%,Rb基因可能的突变率为21%,不同分化程度肿瘤的p53及Rb基因突变率未见明显区别。结论,PCR-SSCP银染技术是筛查基因突变简便、敏感、无核素污染的最佳方法。
Objective: To recognize the mutation status of p53 and Rb cancer suppresor genes. Methods: for the first time, 57 ovarian cancer samples were analysised by PCR for DNA amplification, and then SSCP, furthes PCR DNA sequence. Results:(1) The mutation ratio of p53 in ovarian cancer was 32%, (2) The mutation of Rb gene in ovarian cancer was 21%, (3)Neither p53 nor Rb gene mutation ratio was found significant difference in varions differential stages. Conclusions: PCR SSCP DNA sequence method is the best one in testing gene mutation for its simplicity, sensitivity and no radioisotope contamination. Direct PCR DNA sequence can test point mutation of single amino acid change.
出处
《中国优生与遗传杂志》
1998年第3期15-17,20,共4页
Chinese Journal of Birth Health & Heredity