Triaca Viviana, Fico Elena, Rosso Pamela, Ralli Massimo, Corsi Alessandro, Severini Cinzia, Crevenna Alvaro, Agostinelli Enzo, Rullo Emma, Riminucci Mara, Colizza Andrea, Polimeni Antonella, Greco Antonio, Tirassa Paola
Institute of Biochemistry and Cell Biology, National Research Council (CNR), International Campus A. Buzzati-Traverso, Monterotondo Scalo, 00015 Rome, Italy.
Department of Sense Organs, Institute of Biochemistry and Cell Biology, National Research Council (CNR), University of Rome La Sapienza, 00185 Rome, Italy.
Cancers (Basel). 2022 May 25;14(11):2622. doi: 10.3390/cancers14112622.
We investigated the p75 Neurotrophin Receptor (p75NTR) expression and cleavage product p75NTR Intracellular Domain (p75ICD) as potential oncogenic and metastatic markers in human Laryngeal Squamous Cell Carcinoma (LSCC). p75NTR is highly expressed in Cancer Stem Cells (CSCs) of the laryngeal epithelia and it has been proposed as a marker for stemness, cell migration, and chemo-resistance in different squamous carcinomas. To investigate the clinical significance of p75NTR cleavage products in solid tumors, full-length and cleaved p75NTR expression was analyzed in laryngeal primary tumors from different-stage LSCC patients, diagnosed at the Policlinico Umberto I Hospital. Molecular and histological techniques were used to detect the expressions of p75NTR and p75ICD, and ATP Binding Cassette Subfamily G Member 2 (ABCG2), a CSC marker. We found regulated p75NTR cleavage during squamous epithelial tumor progression and tissue invasion. Our preliminary investigation suggests p75ICD expression and localization as possible features of tumorigenesis and metastaticity. Its co-localization with ABCG2 in squamous cells in the parenchyma invaded by the tumor formation allows us to hypothesize p75NTR and p75ICD roles in tumor invasion and CSC spreading in LSCC patients. These data might represent a starting point for a comprehensive analysis of p75NTR cleavage and of its clinical relevance as a potential molecular LSCC signature, possibly helping diagnosis, and improving prognosis and personalized therapy.
我们研究了p75神经营养因子受体(p75NTR)的表达及其裂解产物p75NTR细胞内结构域(p75ICD),将其作为人类喉鳞状细胞癌(LSCC)潜在的致癌和转移标志物。p75NTR在喉上皮的癌症干细胞(CSC)中高度表达,并且已被提议作为不同鳞状细胞癌中干性、细胞迁移和化疗耐药性的标志物。为了研究p75NTR裂解产物在实体瘤中的临床意义,我们分析了在翁贝托一世综合医院诊断的不同分期LSCC患者喉原发性肿瘤中全长和裂解的p75NTR表达。采用分子和组织学技术检测p75NTR、p75ICD以及一种CSC标志物ATP结合盒亚家族G成员2(ABCG2)的表达。我们发现在鳞状上皮肿瘤进展和组织侵袭过程中p75NTR裂解受到调控。我们的初步研究表明p75ICD的表达和定位可能是肿瘤发生和转移的特征。它与ABCG2在肿瘤形成侵袭的实质鳞状细胞中共定位,这使我们能够推测p75NTR和p75ICD在LSCC患者肿瘤侵袭和CSC扩散中的作用。这些数据可能代表了全面分析p75NTR裂解及其作为潜在分子LSCC标志物的临床相关性的起点,可能有助于诊断,并改善预后和个性化治疗。