Department of Pathology, Soonchunhyang University Cheonan Hospital, Cheonan, Republic of Korea.
Department of Cardiothoracic and Vascular Surgery, Soonchunhyang University Cheonan Hospital, Cheonan, Republic of Korea.
Pathol Res Pract. 2020 Nov;216(11):153156. doi: 10.1016/j.prp.2020.153156. Epub 2020 Aug 8.
Adenine-thymine-rich inactive domain-containing protein 1A (ARID1A) is a large subunit of the switch-sucrose nonfermenting (SWI-SNF) complex. ARID1A is considered to be a tumor suppressor in various cancers. We investigated the clinicopathological significance including prognosis of ARID1A expression in non-small cell lung cancer (NSCLC). ARID1A expression was studied by tissue microarray immunohistochemical analysis of 171 surgically resected NSCLC specimens including adenocarcinoma (ADC) and squamous cell carcinoma (SCC) on tissue microarray. Semiquantitative immunohistochemical score was obtained by multiplying the intensity and percentage scores. The overall score was further simplified by dichotomizing into either negative (score < 4) or positive (score ≥ 4) for each patient. The ARID1A-negative group revealed significantly higher correlations with male sex (p = 0.020), larger tumor size (p = 0.007), SCC than with ADC (p = 0.023) and smoking (p = 0.001). Univariate survival analysis showed that the ARID1A-negative group had a significantly shorter cancer specific survival than the ARID1A-positive group (p = 0.018). Multivariate survival analysis showed that ARID1A negativity (p = 0.022) were independent prognostic factors related with shorter cancer specific survival for NSCLC. In conclusion, Loss of ARID1A expression is a potential molecular marker to predictive of poor prognosis of NSCLC.
富含腺嘌呤-胸腺嘧啶的非活性结构域蛋白 1A(ARID1A)是转换蔗糖非发酵(SWI-SNF)复合物的大亚基。ARID1A 被认为是各种癌症中的肿瘤抑制因子。我们研究了 ARID1A 在非小细胞肺癌(NSCLC)中的表达的临床病理意义,包括预后。通过对 171 例手术切除的 NSCLC 标本(包括腺癌[ADC]和鳞状细胞癌[SCC])的组织微阵列免疫组织化学分析,研究了 ARID1A 的表达。通过将强度和百分比得分相乘获得半定量免疫组织化学评分。通过对每位患者的得分进行二分类(得分<4 为阴性,得分≥4 为阳性),进一步简化总得分。ARID1A 阴性组与男性(p=0.020)、更大的肿瘤大小(p=0.007)、SCC 比 ADC(p=0.023)和吸烟(p=0.001)之间的相关性显著更高。单因素生存分析显示,ARID1A 阴性组的癌症特异性生存率明显低于 ARID1A 阳性组(p=0.018)。多因素生存分析显示,ARID1A 阴性(p=0.022)是与 NSCLC 癌症特异性生存率较短相关的独立预后因素。总之,ARID1A 表达缺失是预测 NSCLC 预后不良的潜在分子标志物。