Al-Maghrabi Jaudah
Jaudah Al-Maghrabi, MD, FRCPC, FCAP. Department of Pathology, Faculty of Medicine, King Abdulaziz University, Jeddah, Saudi Arabia.
Pak J Med Sci. 2021 Jan-Feb;37(1):114-120. doi: 10.12669/pjms.37.1.2592.
The loss of expression of syndecansyndecan-1 is associated with poor prognosis in many types of human cancer. The objective of this study was to evaluate the relation between syndecan-1 immunoexpression and several clinicopathological parameters in a subset of colorectal carcinoma (CRC) patients.
Pathology tissue blocks of 202 primary tumors, 41 adenomas, and 37 normal colonic mucosae were used in this study. The cases diagnosed in the period 1995-2015 was included in the study. Immunohistochemistry analysis was performed using anti-CD138/syndecan-1 (B-A38) mouse monoclonal antibody. A semiquantitative method was used to score the syndecan-1 expression based on an evaluation of the percentage and intensity of the membranous and cytoplasmic expression. The data collected from Pathology Department at King Abdulaziz University Hospital, Jeddah, Saudi Arabia. This is a retrospective cohort study that was conducted from July 2018 until August 2019.
Loss of syndecan-1 immunoexpression was observed in 72 (42.6%), 5 (12.2%), and 3 (8.1%) cases of CRC, adenomas, and normal mucosae, respectively. Low expression of syndecan-1 showed an association with nodal (p=0.003) and distant (p=0.001) metastasis, lymphovascular invasion (p=0.001), and tumor recurrence (p=0.006). Low syndecan-1 expression were associated with short overall survival (OS) (log rank 4.019, p=0.045) and disease-free survival (DFS) probabilities (log rank 4.748, p=0.029).
Loss of syndecan-1 immunoexpression is associated with metastatic potential, tumor recurrence and shorter survival in CRC and is considered a potential biomarker of poor prognosis in CRC patients.
Syndecan-1表达缺失与多种人类癌症的不良预后相关。本研究的目的是评估结直肠癌(CRC)患者亚组中Syndecan-1免疫表达与若干临床病理参数之间的关系。
本研究使用了202例原发性肿瘤、41例腺瘤和37例正常结肠黏膜的病理组织块。研究纳入了1995年至2015年期间诊断的病例。使用抗CD138/Syndecan-1(B-A38)小鼠单克隆抗体进行免疫组织化学分析。基于对膜性和细胞质表达的百分比及强度的评估,采用半定量方法对Syndecan-1表达进行评分。数据收集自沙特阿拉伯吉达阿卜杜勒阿齐兹国王大学医院病理科。这是一项从2018年7月至2019年8月进行的回顾性队列研究。
分别在72例(42.6%)CRC、5例(12.2%)腺瘤和3例(8.1%)正常黏膜病例中观察到Syndecan-1免疫表达缺失。Syndecan-1低表达与淋巴结转移(p=0.003)、远处转移(p=0.001)、淋巴管浸润(p=0.001)及肿瘤复发(p=0.006)相关。Syndecan-1低表达与总生存期(OS)缩短(对数秩检验4.019,p=0.045)和无病生存期(DFS)概率降低(对数秩检验4.748,p=0.029)相关。
Syndecan-1免疫表达缺失与CRC的转移潜能、肿瘤复发及生存期缩短相关,被认为是CRC患者不良预后的潜在生物标志物。