Gorgoulis V G, Koutroumbi E N, Kotsinas A, Zacharatos P, Markopoulos C, Giannikos L, Kyriakou V, Voulgaris Z, Gogas I, Kittas C
Department of Histology and Embryology, School of Medicine, University of Athens, Greece.
Mol Med. 1998 Dec;4(12):807-22.
The p16-pRb pathway represents a vital cell-cycle checkpoint. In the present study we investigated the alterations of this G1-phase protein pathway using immunohistochemical and molecular methods in a series of 55 breast carcinomas and correlated the findings with clinicopathological features of the patients. Furthermore, we examined its relationship with the status of the chromosomal region 9p21-22 performing a deletion map analysis because there are indications that, in addition to CDKN2 and MTS2/p15(INK4B) tumor suppressor genes (TSGs), this area harbors other TSG(s). Aberrant expression (Ab) of p16 and pRb was observed in 26 (47%) and 16 (29%) of the carcinomas, respectively. A statistical trend pointing out an inverse relationship between p16 and pRb expression was found (p = 0.079). Analysis of the region that encodes for p16 by deletion mapping, a PCR-based methylation assay and PCR-SSCP, revealed that deletions and transcriptional silencing by methylation might represent the main mechanisms of CDKN2/p16(INK4A) inactivation in breast carcinomas. The results of deletion mapping also suggest that another TSG(s) may reside at the 9p21-22 area particularly at the D9S162 loci and that co-deletion of this putative gene with CDKN2/p16(INK4A) may play a role in breast carcinogenesis. In addition, microsatellite instability (MI), a marker of replication error phenotype (RER+), was observed with a frequency of 16% in the area examined and was inversely related with loss of heterozygosity (LOH). Interestingly, most cases with MI at the region encoding for p16 were aggregated in a subgroup of breast carcinomas with no other obvious genetic and/or epigenetic CDKN2/p16(INK4A) alterations. We speculate that there is an additional mechanism of CDKN2/p16(INK4A) inactivation. The relationship of p16 protein level pRb, status, the p16-pRb combined immunoprofiles, and the microsatellite alterations detected at the 9p21-22 locus with the patients' clinicopathological parameters revealed two significant correlations: one between normal pRb expression and lymph node involvement (p = 0.0263), and the other between microsatellite alterations (LOH and or MI) and tumor size (p = 9.2 x 10(-3)). In view of the heterogenous nature of breast cancer, we suggest that in a significant proportion of breast carcinomas, deregulation of the p16-pRb pathway in association with another, as-yet unidentified, TSG(s) of the 9p21-22 region may play a role in initiating or progressing the oncogenic procedure, while in other subgroups, alternative molecules may play this role.
p16-pRb通路是一个重要的细胞周期检查点。在本研究中,我们运用免疫组化和分子方法,对55例乳腺癌患者进行了该G1期蛋白通路改变的研究,并将研究结果与患者的临床病理特征进行了关联分析。此外,我们通过缺失图谱分析,研究了其与染色体区域9p21-22状态的关系,因为有迹象表明,除了CDKN2和MTS2/p15(INK4B)肿瘤抑制基因(TSGs)外,该区域还存在其他肿瘤抑制基因。在26例(47%)和16例(29%)癌组织中分别观察到p16和pRb的异常表达(Ab)。发现了一个统计学趋势,表明p16和pRb表达之间呈负相关(p = 0.079)。通过缺失图谱分析、基于PCR的甲基化检测和PCR-SSCP对编码p16的区域进行分析,结果显示缺失和甲基化导致的转录沉默可能是乳腺癌中CDKN2/p16(INK4A)失活的主要机制。缺失图谱分析结果还表明,另一个肿瘤抑制基因可能位于9p21-22区域,特别是在D9S162位点,该假定基因与CDKN2/p16(INK4A)的共同缺失可能在乳腺癌发生过程中起作用。此外,在所检测区域观察到微卫星不稳定性(MI),这是复制错误表型(RER+)的一个标志物,其频率为16%,且与杂合性缺失(LOH)呈负相关。有趣的是,大多数在编码p16区域出现MI的病例聚集在一组没有其他明显遗传和/或表观遗传CDKN2/p16(INK4A)改变的乳腺癌亚组中。我们推测存在CDKN2/p16(INK4A)失活的另一种机制。p16蛋白水平、pRb状态以及p16-pRb联合免疫表型与在9p21-22位点检测到的微卫星改变与患者临床病理参数之间的关系显示出两个显著相关性:一个是正常pRb表达与淋巴结受累之间的相关性(p = 0.0263),另一个是微卫星改变(LOH和/或MI)与肿瘤大小之间的相关性(p = 9.2 x 10(-3))。鉴于乳腺癌具有异质性,我们认为在相当一部分乳腺癌中,p16-pRb通路的失调与9p21-22区域另一个尚未确定的肿瘤抑制基因可能在致癌过程的启动或进展中起作用,而在其他亚组中,可能有其他分子发挥这一作用。