Ingenwerth M, Brandenburg T, Führer-Sakel D, Goetz M, Weber F, Dralle H, Schildhaus H-U, Schmid K W, Theurer S
Institute of Pathology, University Hospital of Essen, University of Duisburg-Essen, Essen, Germany.
Division of Laboratory Research, Department of Endocrinology, Diabetes and Metabolism and Clinical Chemistry, University Hospital Essen, University of Duisburg-Essen, Germany.
Endocr Connect. 2021 Mar;10(3):283-289. doi: 10.1530/EC-20-0611.
Medullary thyroid carcinomas (MTC) are rare and aggressive neuroendocrine tumors of the thyroid. About 70% of MTC are sporadic; approximately 50% of those harbor somatic RET mutation. DLL3 is widely expressed in many neuroendocrine tumors and has been evaluated as a potential therapeutic target. Since stromal desmoplasia in sporadic MTC has been identified as a reliable predictor of aggressive behavior and development of lymph node metastases, a possible correlation of DLL3 expression with the presence of stromal desmoplasia was of particular interest. 59 paraffin-embedded samples of sporadic MTC with (44 cases) and without (15 cases) stromal desmoplasia and known lymph node status were included. DLL3 expression was determined by immunohistochemistry; no expression (0%), low expression (1-49%) and high expression (≥50%) were correlated with clinicopathological data. The proportion of DLL3 positivity was significantly correlated with both stromal desmoplasia (P < 0.0001) and lymph node metastases (P < 0.0001). MTC without stromal desmoplasia consistently lack DLL3 expression. This is the first study to focus on MTC regarding DLL3 expression and the relationship to various factors. Our results demonstrate that expression of DLL3 in MTC represents a reliable surrogate marker for stromal desmoplasia and lymph node metastases and might be an indicator for aggressive clinical behavior. DLL3 expression in ≥50% of tumor cells virtually excludes MTC without stromal desmoplasia. DLL3 was discussed as a potential therapeutic target in malignant tumors of other locations with positive immunohistochemical reaction and might therefore be a new therapeutic option in MTC, as well.
甲状腺髓样癌(MTC)是一种罕见的侵袭性甲状腺神经内分泌肿瘤。约70%的MTC为散发性;其中约50%存在体细胞RET突变。DLL3在许多神经内分泌肿瘤中广泛表达,并已被评估为潜在的治疗靶点。由于散发性MTC中的间质纤维组织增生已被确定为侵袭性行为和淋巴结转移发生的可靠预测指标,因此DLL3表达与间质纤维组织增生的存在之间可能的相关性尤其令人关注。纳入了59例有(44例)和无(15例)间质纤维组织增生且已知淋巴结状态的散发性MTC石蜡包埋样本。通过免疫组织化学测定DLL3表达;无表达(0%)、低表达(1 - 49%)和高表达(≥50%)与临床病理数据相关。DLL3阳性比例与间质纤维组织增生(P < 0.0001)和淋巴结转移(P < 0.0001)均显著相关。无间质纤维组织增生的MTC始终缺乏DLL3表达。这是第一项关注MTC中DLL3表达及其与各种因素关系的研究。我们的结果表明,MTC中DLL3的表达代表了间质纤维组织增生和淋巴结转移的可靠替代标志物,可能是侵袭性临床行为的一个指标。肿瘤细胞中≥50%表达DLL3实际上可排除无间质纤维组织增生的MTC。DLL3在免疫组化反应阳性的其他部位恶性肿瘤中被讨论为潜在的治疗靶点,因此也可能是MTC的一种新的治疗选择。