Cai Kathy Q, Wu Hong, Klein-Szanto Andres J, Xu Xiang-Xi
Ovarian Cancer Programs, Fox Chase Cancer Center, Philadelphia, PA 19111, USA.
Gynecol Oncol. 2009 Jul;114(1):18-25. doi: 10.1016/j.ygyno.2009.03.023. Epub 2009 Apr 16.
Tp53 mutation is frequent and associates with malignant, high-grade ovarian cancer. However, the details about the progression of Tp53 mutation from heterozygous to homozygous, and association between genotypes and morphological transformation are not clear. We further investigated the expression and mutation of Tp53 and associated markers such as p21 and HDM2 in ovarian cancer.
Areas of contiguous ovarian surface epithelia linking morphological normal monolayer to multilayer neoplastic cells were analyzed for the correlation of Tp53 pathway alteration in relation to morphological transformation, by immunostaining and sequencing of Tp53 gene in cells from laser captured microdissection.
Consistent with previous reports, Tp53 staining is positive in 78% of the tumors. The staining of p21 is positive in about 12%, and HMD2 is positive in only 1% of the tumors. In 9 out of 10 cases of p21-positive tumors, p53 is also positive. In the majority of cases of epithelial histological transitions, overexpression of Tp53 correlates with morphological transformation: Tp53 is negative in monolayered cells and positive in neoplastic lesions. Morphological transformation also closely correlates with cell proliferation as indicated by Ki-67 staining and loss of p21 expression. We detected heterozygous mutation of Tp53 in the monolayers adjacent to neoplastic cells.
p21 expression is an indicator of a wild type Tp53 and lack of p21 in the presence of Tp53 expression predicts an inactivated Tp53. Tp53 inactivation immediately precedes morphological transformation of the ovarian surface epithelium in most cases, and the histological transitional epithelia containing a heterozygous Tp53 mutation are thus pre-neoplastic lesions. We propose that the loss of a second allele of Tp53 leading to the loss of p21 expression, and subsequent cell proliferation, compose a sequence of events that lead to morphological transformation and instigation of ovarian epithelial tumor development.
Tp53突变在恶性、高级别卵巢癌中很常见且与之相关。然而,Tp53突变从杂合子发展到纯合子的具体情况,以及基因型与形态学转变之间的关联尚不清楚。我们进一步研究了卵巢癌中Tp53及其相关标志物如p21和HDM2的表达与突变情况。
通过对激光捕获显微切割获取的细胞进行免疫染色和Tp53基因测序,分析连接形态学上正常的单层卵巢表面上皮细胞与多层肿瘤细胞的连续区域,以探讨Tp53信号通路改变与形态学转变的相关性。
与先前报道一致,78%的肿瘤中Tp53染色呈阳性。p21染色阳性的肿瘤约占12%,而HMD2染色阳性的肿瘤仅占1%。在10例p21阳性肿瘤中有9例p53也呈阳性。在大多数上皮组织学转变的病例中,Tp53的过表达与形态学转变相关:Tp53在单层细胞中呈阴性,而在肿瘤病变中呈阳性。形态学转变也与Ki-67染色所示的细胞增殖以及p21表达缺失密切相关。我们在肿瘤细胞相邻的单层细胞中检测到了Tp53的杂合突变。
p21表达是野生型Tp53的一个指标,在Tp53表达存在的情况下p21缺失预示Tp53失活。在大多数情况下,Tp53失活紧接着卵巢表面上皮的形态学转变,因此含有杂合Tp53突变的组织学过渡性上皮是癌前病变。我们提出,Tp53第二个等位基因的缺失导致p21表达丧失,随后细胞增殖,构成了一系列导致形态学转变和引发卵巢上皮肿瘤发生的事件。