胰岛素瘤相关蛋白1(INSM1)的高表达将结直肠癌混合和纯神经内分泌癌与突触素弥漫表达的传统腺癌区分开来。

IF 3.4 2区 医学 Q1 PATHOLOGY
Anne-Sophie Litmeyer, Björn Konukiewitz, Atsuko Kasajima, Sebastian Foersch, Felix Schicktanz, Maxime Schmitt, Franziska Kellers, Albert Grass, Paul Jank, Bettina Lehman, Thomas M Gress, Anja Rinke, Detlef K Bartsch, Carsten Denkert, Wilko Weichert, Günter Klöppel, Moritz Jesinghaus
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引用次数: 0

摘要

与突触素和嗜铬粒蛋白A互补的胰岛素瘤相关蛋白1(INSM1)已成为诊断神经内分泌肿瘤的敏感标志物。由于没有关于INSM1在传统结直肠癌(CRC)和结直肠癌混合腺神经内分泌癌/神经内分泌癌(MANECs/NECs)中表达的比较数据,我们在传统CRC和MANECs/NECs的大队列中检测了INSM1。在传统CRC中,我们特别关注突触素弥漫性表达的传统CRC,突触素有被误解为MANEC或NEC的风险。我们根据1033个常规CRC和21个MANECs/NECs的主要队列中的免疫反应评分,与突触素和嗜铬粒蛋白A的表达进行比较,研究了INSM1,并将结果与临床病理参数和患者生存率相关联。所有MANECs/NECs都表达INSM1,通常表现出高或中等表达(57%高,34%中等,9%低),这将它们与传统CRC区分开来,传统CRC通常为INSM1阴性或低,即使它们广泛表达突触素。在常规CRC中未观察到INSM1的高表达。嗜铬粒蛋白A在大多数常规CRC中呈阴性/低水平(99%),但在大多数MANEC/NEC中也呈阴性(66%)。在我们的传统CRC(n = 274)和MANEC/NEC(n = 19) 。与突触素类似,INSM1的表达在传统CRC中与预后无关,而真正的MANEC/NEC在单变量和多变量分析中显示出高度受损的生存率(例如,疾病特异性生存率:p
本文章由计算机程序翻译,如有差异,请以英文原文为准。

High expression of insulinoma-associated protein 1 (INSM1) distinguishes colorectal mixed and pure neuroendocrine carcinomas from conventional adenocarcinomas with diffuse expression of synaptophysin

High expression of insulinoma-associated protein 1 (INSM1) distinguishes colorectal mixed and pure neuroendocrine carcinomas from conventional adenocarcinomas with diffuse expression of synaptophysin

Complementary to synaptophysin and chromogranin A, insulinoma-associated protein 1 (INSM1) has emerged as a sensitive marker for the diagnosis of neuroendocrine neoplasms. Since there are no comparative data regarding INSM1 expression in conventional colorectal adenocarcinomas (CRCs) and colorectal mixed adenoneuroendocrine carcinomas/neuroendocrine carcinomas (MANECs/NECs), we examined INSM1 in a large cohort of conventional CRCs and MANECs/NECs. In conventional CRC, we put a special focus on conventional CRC with diffuse expression of synaptophysin, which carry the risk of being misinterpreted as a MANEC or a NEC. We investigated INSM1 according to the immunoreactive score in our main cohort of 1,033 conventional CRCs and 21 MANECs/NECs in comparison to the expression of synaptophysin and chromogranin A and correlated the results with clinicopathological parameters and patient survival. All MANECs/NECs expressed INSM1, usually showing high or moderate expression (57% high, 34% moderate, and 9% low), which distinguished them from conventional CRCs, which were usually INSM1 negative or low, even if they diffusely expressed synaptophysin. High expression of INSM1 was not observed in conventional CRCs. Chromogranin A was negative/low in most conventional CRCs (99%), but also in most MANECs/NECs (66%). Comparable results were observed in our independent validation cohorts of conventional CRC (n = 274) and MANEC/NEC (n = 19). Similar to synaptophysin, INSM1 expression had no prognostic relevance in conventional CRCs, while true MANEC/NEC showed a highly impaired survival in univariate and multivariate analyses (e.g. disease-specific survival: p < 0.001). MANECs/NECs are a highly aggressive variant of colorectal cancer, which must be reliably identified. High expression of INSM1 distinguishes MANEC/NEC from conventional CRCs with diffuse expression of the standard neuroendocrine marker synaptophysin, which do not share the same dismal prognosis. Therefore, high INSM1 expression is a highly specific/sensitive marker that is supportive for the diagnosis of true colorectal MANEC/NEC.

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来源期刊
Journal of Pathology Clinical Research
Journal of Pathology Clinical Research Medicine-Pathology and Forensic Medicine
CiteScore
7.40
自引率
2.40%
发文量
47
审稿时长
20 weeks
期刊介绍: The Journal of Pathology: Clinical Research and The Journal of Pathology serve as translational bridges between basic biomedical science and clinical medicine with particular emphasis on, but not restricted to, tissue based studies. The focus of The Journal of Pathology: Clinical Research is the publication of studies that illuminate the clinical relevance of research in the broad area of the study of disease. Appropriately powered and validated studies with novel diagnostic, prognostic and predictive significance, and biomarker discover and validation, will be welcomed. Studies with a predominantly mechanistic basis will be more appropriate for the companion Journal of Pathology.
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