Petterino Claudio, Ratto Alessandra, Podestà Giorgia, Drigo Michele, Pellegrino Claudio
Department of Public Health, Comparative Pathology and Veterinary Hygiene School of Veterinary Medicine, University of Padua, Agripolis, Legnaro, Italy.
Res Vet Sci. 2007 Apr;82(2):218-24. doi: 10.1016/j.rvsc.2006.06.010. Epub 2006 Aug 24.
STAT3 (signal transducer and activator of transcription 3) is a cytoplasmic transcription factor that plays a role in the G1 to S phase cell-cycle transition and is induced by cytokines and growth factors. The expression of STAT3 phosphorylated on tyrosine 705 (STAT3-p-tyr705) in normal, hyperplastic and neoplastic feline mammary gland tissue was assessed by immunohistochemistry in 45 cats. The samples included 4 normal mammary non-lactating tissues, 9 hyperplastic tissues (5 fibroepithelial hyperplasia and 4 lobular epithelial hyperplasia), 2 benign tumours (1 complex adenoma, and 1 simple adenoma), and 30 carcinomas (18 simple tubular papillary, 6 simple tubular, 2 simple solid, 3 cribriform, and 1 adenosquamous carcinoma). For immunohistochemistry, tissue sections were incubated with an anti-STAT3-p-tyr705 monoclonal antibody and visualized with EnVision-DAB polymer. STAT3-p-tyr705 positivity was quantified in a semi-quantitative manner. All positive samples showed cytoplasmic and/or nuclear positivity. Normal non-lactating mammary tissue showed a low number of positive cells, similar to hyperplastic tissue. In neoplastic tissues, a high number of positive cells with a moderate to intense reaction was observed. Moreover, a correlation was observed between nuclear positivity for STAT3-p-tyr705 and histologic grade (P=0.013; r=0.447), tubular formation (P=0.043; r=0.820), and mitotic activity (P<0.0001; r=0.689). In contrast, no such correlations were observed for cytoplasmic reactivity of STAT3-p-tyr705. A significant difference was observed between malignant lesions and hyperplasia with regards to expression of STAT3-p-tyr 705 in the cytoplasm (P=0.008; U=59.00) and nuclei (P=0.002; U=47.00). These results confirm previous our data and reinforce the potential role of STAT3 in malignancy as reported for human breast cancer and other sporadic tumours.
信号转导与转录激活因子3(STAT3)是一种细胞质转录因子,在G1期到S期的细胞周期转换中发挥作用,可被细胞因子和生长因子诱导。通过免疫组织化学方法,对45只猫的正常、增生和肿瘤性猫乳腺组织中酪氨酸705位点磷酸化的STAT3(STAT3-p-tyr705)的表达进行了评估。样本包括4个正常非泌乳乳腺组织、9个增生组织(5个纤维上皮增生和4个小叶上皮增生)、2个良性肿瘤(1个复合腺瘤和1个单纯腺瘤)以及30个癌(18个单纯管状乳头状癌、6个单纯管状癌、2个单纯实性癌、3个筛状癌和1个腺鳞癌)。对于免疫组织化学,将组织切片与抗STAT3-p-tyr705单克隆抗体孵育,并用EnVision-DAB聚合物显色。以半定量方式对STAT3-p-tyr705阳性进行定量。所有阳性样本均显示细胞质和/或细胞核阳性。正常非泌乳乳腺组织显示阳性细胞数量较少,与增生组织相似。在肿瘤组织中,观察到大量阳性细胞,反应程度为中度至强烈。此外,还观察到STAT3-p-tyr705的细胞核阳性与组织学分级(P=0.013;r=0.447)、管状形成(P=0.043;r=0.820)以及有丝分裂活性(P<0.0001;r=0.689)之间存在相关性。相比之下,未观察到STAT-3-p-tyr705的细胞质反应性存在此类相关性。在细胞质(P=0.008;U=59.00)和细胞核(P=0.002;U=47.00)中,恶性病变与增生之间在STAT3-p-tyr705的表达方面存在显著差异。这些结果证实了我们之前的数据,并强化了STAT3在恶性肿瘤中的潜在作用,这与人类乳腺癌和其他散发性肿瘤的报道一致。