Kupryjanczyk J, Bell D A, Dimeo D, Beauchamp R, Thor A D, Yandell D W
Department of Pathology, Harvard Medical School, Boston, MA, USA.
Hum Pathol. 1995 Apr;26(4):387-92. doi: 10.1016/0046-8177(95)90138-8.
Mutations of the p53 gene are common in human ovarian carcinomas; however, their role in the early development of ovarian cancer is unclear. Twelve ovarian borderline tumors (BTs; eight of them p53 immunopositive) and 10 stage I carcinomas (four of them p53 immunopositive) were studied for genetic alterations in the p53 gene. The study was based on single-strand conformation polymorphism (SSCP) analysis and DNA sequencing of exons 2 through 11 of the p53 gene using DNA preparations from microdissected tumors. Mutations were found in 40% of the carcinomas (including a borderline component adjacent to carcinoma in one lesion) but in none of the pure BTs. These findings suggest that p53 mutations may not be commonly associated with the borderline phenotype of ovarian epithelial tumors but may occur during malignant transformation.
p53基因的突变在人类卵巢癌中很常见;然而,它们在卵巢癌早期发展中的作用尚不清楚。对12例卵巢交界性肿瘤(BTs;其中8例p53免疫阳性)和10例I期癌(其中4例p53免疫阳性)进行了p53基因的基因改变研究。该研究基于单链构象多态性(SSCP)分析以及使用显微切割肿瘤的DNA制备物对p53基因第2至11外显子进行DNA测序。在40%的癌中发现了突变(包括一个病变中与癌相邻的交界性成分),但在所有纯BTs中均未发现突变。这些发现表明,p53突变可能与卵巢上皮性肿瘤的交界性表型通常无关,但可能在恶性转化过程中发生。