Lee Sung Hak, Choi Eun Ji, Kim Min Sik, Park Jun Wook, Lee Youn Soo, Kim Su Young, Kang Chang Suk
Department of Hospital Pathology, College of Medicine, The Catholic University of Korea, Banpodaero 222 Socho-gu, Seoul, 137-701, Korea.
Int J Clin Oncol. 2014 Apr;19(2):247-53. doi: 10.1007/s10147-013-0552-7. Epub 2013 Apr 4.
Syndecan-1 (SDC1) is reported to modulate several key processes of tumorigenesis and to show variable expression in many cancers. The cause of these variations in expression is not known to date. In this study, we compared SDC1 status with clinicopathologic parameters to evaluate the prognostic implications of SDC1 status on squamous cell carcinoma (SCC) of the tonsil.
In 56 cases of tonsillar SCC, we screened SDC1 expression using immunohistochemistry and analyzed the relationships between SDC1 expression and clinicopathological parameters. To identify the cause of the changes in SDC1 expression seen in tumors, we measured the gene dosage of SDC1 in tumor cells using fluorescent in situ hybridization.
SDC1 expression was found in cancer cells in 36 cases (64.3 %) of tonsillar SCC. It was associated with lymph node metastasis (p = 0.010) and a positive surgical resection margin (p = 0.014). On the other hand, it was not significantly correlated with sex, age, smoking status, degree of differentiation, T stage, or distant metastasis. We could not find any copy-number variation of SDC1 in the cases showing increased SDC1 immunopositivity. In addition, strong SDC1 expression in the tumor cells predicted a shorter overall survival (p = 0.020, log-rank).
We showed that SDC1 expression is associated with N stage and the status of resection margin involvement in SCC of the tonsil. With respect to survival, there were unfavorable outcomes in cases with SDC1 positivity. More studies are needed to better understand the role of SDC1 in the progression and invasiveness of tonsillar SCC.
据报道,Syndecan-1(SDC1)可调节肿瘤发生的几个关键过程,并且在许多癌症中表现出可变表达。迄今为止,这些表达变化的原因尚不清楚。在本研究中,我们将SDC1状态与临床病理参数进行比较,以评估SDC1状态对扁桃体鳞状细胞癌(SCC)的预后影响。
在56例扁桃体SCC病例中,我们使用免疫组织化学筛选SDC1表达,并分析SDC1表达与临床病理参数之间的关系。为了确定肿瘤中SDC1表达变化的原因,我们使用荧光原位杂交测量肿瘤细胞中SDC1的基因剂量。
在36例(64.3%)扁桃体SCC的癌细胞中发现了SDC1表达。它与淋巴结转移(p = 0.010)和手术切缘阳性(p = 0.014)相关。另一方面,它与性别、年龄、吸烟状况、分化程度、T分期或远处转移无显著相关性。在显示SDC1免疫阳性增加的病例中,我们未发现SDC1的任何拷贝数变异。此外,肿瘤细胞中SDC1的强表达预示着总生存期较短(p = 0.020,对数秩检验)。
我们表明,SDC1表达与扁桃体SCC的N分期和切缘受累状态相关。就生存而言,SDC1阳性的病例预后不良。需要更多的研究来更好地了解SDC1在扁桃体SCC进展和侵袭中的作用。