Department of Pathology, Ambroise Paré Hospital, APHP, Boulogne, France.
Department of Pathology, Hotel Dieu, Nantes, France.
Cancer Biomark. 2020;27(3):399-406. doi: 10.3233/CBM-190287.
SMARCB1 is a tumor suppressor gene, which is part of SWI/SNF complex involved in transcriptional regulation. Recently, loss of SMARCB1 expression has been reported in gastrointestinal carcinomas. Our purpose was to evaluate the incidence and prognostic value of SMARCB1 loss in colon carcinoma (CC). Patients with stage III CC (n= 1695), and a second cohort of 23 patients with poorly differentiated CC were analyzed. Immunohistochemistry for SMARCB1 was performed on tissue microarrays, and cases with loss of expression were controlled on whole sections. Loss of SMARCB1 was compared with the clinico-pathological and molecular characteristics, and the prognostic value was evaluated. Loss of SMARCB1 was identified in 12 of 1695 (0.7%) patients with stage III CC. Whole section controls showed a complete loss in only one of these cases, corresponding to a medullary carcinoma. SMARCB1 loss was not associated with histological grade, tumor size nor survival. In the cohort of poorly differentiated CC, we detected 2/23 (8.7%) cases with loss of SMARCB1; one was rhabdoid while the other had medullary and mucinous histology. These 2 cases were deficient for MisMatched Repair (dMMR) and mutated for BRAF. SMARCB1 loss is rare in stage III CC, but appears more frequent in poorly differentiated CC.
SMARCB1 是一种肿瘤抑制基因,它是参与转录调控的 SWI/SNF 复合物的一部分。最近,胃肠道癌中报道了 SMARCB1 表达缺失。我们的目的是评估 SMARCB1 缺失在结肠癌(CC)中的发生率和预后价值。对 III 期 CC(n=1695)患者和 23 例低分化 CC 患者的第二个队列进行了分析。在组织微阵列上进行了针对 SMARCB1 的免疫组织化学检测,并对表达缺失的病例进行了全切片对照。将 SMARCB1 的缺失与临床病理和分子特征进行了比较,并评估了其预后价值。在 1695 例 III 期 CC 患者中,发现 12 例(0.7%)存在 SMARCB1 缺失。全切片对照仅在其中一个病例中显示完全缺失,对应于髓样癌。SMARCB1 缺失与组织学分级、肿瘤大小或生存无关。在低分化 CC 队列中,我们检测到 2/23(8.7%)例 SMARCB1 缺失;其中 1 例为横纹肌样,另 1 例具有髓样和粘液样组织学特征。这 2 例均存在错配修复缺陷(dMMR)和 BRAF 突变。SMARCB1 缺失在 III 期 CC 中罕见,但在低分化 CC 中更为常见。