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磷酸化信号转导子和转录激活子 3 的表达及其在犬肛门囊腺癌中的预后意义。

Expression of Phosphorylated Signal Transducer and Activator of Transcription 3 and its Prognostic Significance in Canine Anal Sac Adenocarcinoma.

机构信息

The Queen's Veterinary School Hospital, Cambridge University Veterinary School, Cambridge, UK.

The Queen's Veterinary School Hospital, Cambridge University Veterinary School, Cambridge, UK.

出版信息

J Comp Pathol. 2021 Jan;182:15-21. doi: 10.1016/j.jcpa.2020.11.002. Epub 2020 Dec 5.

DOI:10.1016/j.jcpa.2020.11.002
PMID:33494902
Abstract

Prognostication in canine anal sac adenocarcinomas (ASACs) is difficult due to conflicting evidence regarding metastatic rates and median survival times (MSTs). The transcription factor signal transducer and activator of transcription 3 (STAT3) is a prognostic predictor in several human cancers. The aim of this retrospective study was to assess STAT3 expression in ASACs and to explore its association with clinical presentation and outcome. We hypothesized that STAT3 expression would distinguish tumours with early versus late metastasis. Records from The Queen's Veterinary School Hospital, Cambridge, UK, were searched for dogs diagnosed with ASAC from 2008 to 2019. Immunohistochemical expression of phosphorylated STAT3 (pSTAT3) was assessed in primary tumours (n = 57) and metastatic lymph nodes (n = 30) and MSTs were calculated for cases with low and high pSTAT3 expression. Of the 57 cases assessed, 27 presented with primary tumours but no metastasis and 30 with both primary and local metastatic disease. Most cases (50/57) expressed nuclear pSTAT3 within neoplastic cells in both primary tumour and metastatic lymph nodes. pSTAT3 expression was predominantly observed in neoplastic cells at the edges of neoplastic lobules, suggesting a potential role in invasion. There was no significant difference in pSTAT3 expression between cases metastatic at presentation and those that did not have detectable metastasis at presentation. There was no significant difference between the MSTs in cases with high and low pSTAT3 expression. Cases that presented with metastatic disease had shorter MSTs (395 days) than those with primary tumours alone (623 days). Although pSTAT3 is variably expressed in primary and metastatic ASAC cells, pSTAT3 did not provide prognostic information for canine ASAC.

摘要

由于关于转移率和中位生存时间 (MST) 的证据相互矛盾,犬肛门囊腺癌 (ASAC) 的预后预测较为困难。转录因子信号转导子和转录激活子 3 (STAT3) 是几种人类癌症的预后预测因子。本回顾性研究旨在评估 ASAC 中的 STAT3 表达,并探讨其与临床表现和结果的关系。我们假设 STAT3 表达将区分具有早期和晚期转移的肿瘤。从英国剑桥的女王兽医学校医院的记录中搜索了 2008 年至 2019 年诊断为 ASAC 的狗。在原发肿瘤 (n=57) 和转移性淋巴结 (n=30) 中评估磷酸化 STAT3 (pSTAT3) 的免疫组织化学表达,并计算低表达和高表达 pSTAT3 的病例的 MST。在评估的 57 例病例中,27 例表现为原发性肿瘤但无转移,30 例表现为原发性和局部转移性疾病。大多数病例 (50/57) 在原发肿瘤和转移性淋巴结中的肿瘤细胞中表达核内 pSTAT3。pSTAT3 表达主要观察到在肿瘤小叶边缘的肿瘤细胞中,提示其在侵袭中具有潜在作用。在有或没有可检测到的转移性疾病的病例中,pSTAT3 的表达没有显著差异。高表达和低表达 pSTAT3 的病例之间的 MST 没有显著差异。有转移性疾病的病例的 MST 较短 (395 天),而只有原发性肿瘤的病例的 MST 较长 (623 天)。尽管 pSTAT3 在原发性和转移性 ASAC 细胞中均有不同程度的表达,但 pSTAT3 并未为犬 ASAC 提供预后信息。

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