Shibahara Yukiko, Espin-Garcia Osvaldo, Conner James, Weiss Jessica, Derouet Mathieu, Allen Jonathan, Allison Frances, Kalimuthu Sangeetha, Yeung Jonathan C, Darling Gail E
Latner Thoracic Surgery Research Laboratories, University Health Network, Toronto, CAN.
Department of Pathology, Laboratory Medicine Program, University Health Network, University of Toronto, Toronto, CAN.
Cureus. 2022 Jan 7;14(1):e21021. doi: 10.7759/cureus.21021. eCollection 2022 Jan.
Purpose Intestinal stem cell markers play a significant role in esophageal adenocarcinoma carcinogenesis via Barrett's esophagus; however, its utility as a prognostic biomarker has not been established. Methods We analyzed the immunohistochemical expression of intestinal stem cell markers, ASCL2 and LGR5, using whole slides (35 cases) and tissue microarray (TMA; 64 cases). On TMA slides, adjacent normal squamous epithelium, metaplastic glandular epithelium (Barrett's esophagus), and dysplastic glandular epithelium were inserted when applicable. Two pathologists semi-quantitatively scored stained slides independently, and the results were correlated with clinicopathologic factors and outcomes. Results In whole slides, 51% and 57% expressed high ASCL2 and high LGR5; in TMA, 69% and 88% expressed high ASCL2 and high LGR5, respectively. In TMA, high ASCL2 and low LGR5 expression significantly correlated to a higher number of involved lymph nodes (p=0.027 and p=0.0039), and LGR5 expression significantly correlated to the pathological stage (p=0.0032). Kaplan-Meier analysis showed a negative impact of high ASCL2 expression on overall survival (OS; WS p=0.0168, TMA p=0.0276) as well as progression-free survival (PFS; WS p=0.000638, TMA p=0.0466) but not LGR5. Multivariate Cox regression analysis revealed that ASCL2 expression is an independent prognostic factor for esophageal adenocarcinoma (OS; WS p=0.25, TMA p=0.011. PFS; WS p=0.012, TMA p=0.038). Analysis of the TCGA dataset showed that ASCL2 mRNA levels were correlated to nodal status but not overall survival. Conclusion High expression of the intestinal stem cell marker ASCL2 may predict unfavorable outcomes in surgically resected esophageal adenocarcinoma.
目的 肠道干细胞标志物在通过巴雷特食管发生的食管腺癌致癌过程中发挥重要作用;然而,其作为预后生物标志物的效用尚未确立。方法 我们使用全切片(35例)和组织微阵列(TMA;64例)分析了肠道干细胞标志物ASCL2和LGR5的免疫组化表达。在TMA切片上,适当时插入相邻的正常鳞状上皮、化生腺上皮(巴雷特食管)和发育异常腺上皮。两名病理学家独立对染色切片进行半定量评分,结果与临床病理因素和预后相关。结果 在全切片中,51%和57%表达高ASCL2和高LGR5;在TMA中,分别有69%和88%表达高ASCL2和高LGR5。在TMA中,高ASCL2和低LGR5表达与更多的受累淋巴结显著相关(p=0.027和p=0.0039),且LGR5表达与病理分期显著相关(p=0.0032)。Kaplan-Meier分析显示高ASCL2表达对总生存期(OS;全切片p=0.0168,TMA p=0.0276)以及无进展生存期(PFS;全切片p=0.000638,TMA p=0.0466)有负面影响,但对LGR5无影响。多变量Cox回归分析显示ASCL2表达是食管腺癌的独立预后因素(OS;全切片p=0.25,TMA p=0.011。PFS;全切片p=0.012,TMA p=0.038)。对TCGA数据集的分析表明ASCL2 mRNA水平与淋巴结状态相关,但与总生存期无关。结论 肠道干细胞标志物ASCL2的高表达可能预示手术切除的食管腺癌预后不良。