Farabegoli F, Ceccarelli C, Santini D, Taffurelli M
Department of Experimental Pathology, University of Bologna, Via San Giacomo, 14, 40126 Bologna, Italy.
J Clin Pathol. 2005 Oct;58(10):1046-50. doi: 10.1136/jcp.2004.024919.
To investigate SOCS-2 (suppressor of cytokine signalling 2) protein expression in breast carcinoma samples in relation to biopathological parameters and survival.
A polyclonal antibody against SOCS-2 was used to study 50 archival breast carcinoma samples, collected from 1993 to 1995. The presence of SOCS-2 protein was investigated in relation to clinical and biological parameters used in breast cancer pathology. Fluorescence in situ hybridisation (FISH) was used to study whether SOCS-2 expression was related to SOCS-2 gene copy number.
SOCS-2 protein was expressed in 34 of 50 breast carcinoma samples and was positively associated with low grade, low nuclear grade, and p27 protein. SOCS-2 expression was inversely related to Ki-67, cyclin A, retinoblastoma protein (pRb), and the epidermal growth factor receptor (EGFR). No relation with overall survival was demonstrated. SOCS-2 amplification was found in three samples. No relation between the number of FISH signals and SOCS-2 expression was found.
The significant correlation seen between SOCS-2 expression, grade, nuclear grade, p27, Ki-67, cyclin A, pRb, and EGFR labelling strongly supports the hypothesis that SOCS-2 loss might be related to cell proliferation and tumour growth in breast carcinoma. Gene copy number changes did not seem to play a role in SOCS-2 regulation and expression; other mechanisms might be involved and deserve further study.
研究细胞因子信号转导抑制因子2(SOCS-2)蛋白在乳腺癌样本中的表达与生物病理学参数及生存情况的关系。
使用抗SOCS-2的多克隆抗体研究1993年至1995年收集的50份存档乳腺癌样本。研究SOCS-2蛋白的存在情况与乳腺癌病理学中使用的临床和生物学参数的关系。采用荧光原位杂交(FISH)技术研究SOCS-2表达是否与SOCS-2基因拷贝数相关。
50份乳腺癌样本中有34份表达SOCS-2蛋白,且与低级别、低核级别及p27蛋白呈正相关。SOCS-2表达与Ki-67、细胞周期蛋白A、视网膜母细胞瘤蛋白(pRb)及表皮生长因子受体(EGFR)呈负相关。未发现与总生存期有关。在3份样本中发现SOCS-2扩增。未发现FISH信号数量与SOCS-2表达之间的关系。
SOCS-2表达与级别、核级别、p27、Ki-67、细胞周期蛋白A、pRb及EGFR标记之间的显著相关性有力地支持了以下假设:SOCS-2缺失可能与乳腺癌的细胞增殖和肿瘤生长有关。基因拷贝数变化似乎在SOCS-2的调控和表达中不起作用;可能涉及其他机制,值得进一步研究。