Marquet Benjamin, Marchal Bressenot Aude, Fichel Caroline, Bouland Nicole, Barbe Coralie, Bouché Olivier, Kianmanesh Reza, Diebold Marie-Danièle, Boulagnon-Rombi Camille
Department of Biopathology, Academic Hospital, rue du Général Koenig, 51100, Reims, France.
Department of Pathology, Medicine University, Reims, France.
Pathol Oncol Res. 2020 Oct;26(4):2509-2521. doi: 10.1007/s12253-020-00857-5. Epub 2020 Jun 24.
Describe clinical, histological and molecular charatcteristics and prognosis values of the serrated candidate markers AnnexinA10 and Gremlin1 in colon adenocarcinomas. Immunohistochemical expression of AnnexinA10 and Gremlin1 was evaluated on 346 colonic adenocarcinomas. Clinicopathological, molecular features and prognostic characteristics were then evaluated. A total of 40 colonic adenocarcinomas expressed AnnexinA10 (11.6%) and, 115 expressed Gremlin1 (40.4%). AnnexinA10 expression was significantly associated, on univariate analyses, with female gender (p = 0.03), right tumor location (p < 0.001), differentiation grade 3 (p < 0.001), serrated adenocarcinoma subtype (p < 0.001), serrated (p < 0.001), medullary (p = 0.005), and mucinous component (p = 0.004), cytoplasmic eosinophilia (p < 0.001), discernible nuclei (p = 0.001), preserved polarity (p < 0.001), lymphatic invasion (p = 0.01), BRAFV600E mutation (p < 0.001), MSI-H status (p < 0.001) and CIMP-H status (p = 0.019). Multivariate analyses revealed that mucinous component (p = 0.002), lymphatic invasion (p = 0.02) and BRAFV600E mutation (p < 0.001) were independently associated with AnnexinA10 expression. In addition, AnnexinA10 was an indicator of poorer overall survival (OS) in UICC stage IV adenocarcinomas (p = 0.01) only. Gremlin1 expression was neither associated with serrated adenocarcinoma subtype (p = 0.51) nor with AnnexinA10 expression (p = 0,31), but was significantly associated, in univariate analysis with male gender (p = 0.002), younger age (p = 0.002), left tumor location (p = 0.04), and MSS status (p = 0.03). Gremlin1 expression was associated with better OS only in UICC stage III colon adenocarcinomas (p = 0.006). Colon adenocarcinomas expressing AnnexinA10 have distinct clinico-pathological and molecular features. AnnexinA10 expression is an indicator of poorer OS in UICC stage IV patients. Gremlin1 expression is not associated with serrated adenocarcinomas subtype. Its expression was associated with better OS in UICC Stage III patients.
描述锯齿状候选标志物膜联蛋白A10(AnnexinA10)和Gremlin1在结肠腺癌中的临床、组织学及分子特征和预后价值。对346例结肠腺癌进行AnnexinA10和Gremlin1的免疫组化表达评估。然后评估临床病理、分子特征及预后特征。共有40例结肠腺癌表达AnnexinA10(11.6%),115例表达Gremlin1(40.4%)。单因素分析显示,AnnexinA10表达与女性性别(p = 0.03)、肿瘤位于右侧(p < 0.001)、分化3级(p < 0.001)、锯齿状腺癌亚型(p < 0.001)、锯齿状(p < 0.001)、髓样(p = 0.005)和黏液成分(p = 0.004)、细胞质嗜酸性(p < 0.001)、可见细胞核(p = 0.001)、极性保留(p < 0.001)、淋巴浸润(p = 0.01)、BRAFV600E突变(p < 0.001)、微卫星高度不稳定(MSI-H)状态(p < 0.001)及高甲基化表型(CIMP-H)状态(p = 0.019)显著相关。多因素分析显示,黏液成分(p = 0.002)、淋巴浸润(p = 0.02)和BRAFV600E突变(p < 0.001)与AnnexinA10表达独立相关。此外,AnnexinA10仅是UICC IV期腺癌患者总生存期(OS)较差的一个指标(p = 0.01))。Gremlin1表达既与锯齿状腺癌亚型无关(p = 0.51),也与AnnexinA10表达无关(p = 0.31),但在单因素分析中与男性性别(p = 0.002)、较年轻年龄(p = 0.002)、肿瘤位于左侧(p = 0.04)及微卫星稳定(MSS)状态(p = 0.03)显著相关。Gremlin1表达仅在UICC III期结肠腺癌患者中与较好的OS相关(p = 0.006)。表达AnnexinA10的结肠腺癌具有独特的临床病理和分子特征。AnnexinA10表达是UICC IV期患者OS较差的一个指标。Gremlin1表达与锯齿状腺癌亚型无关。其表达在UICC III期患者中与较好的OS相关。