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Cleaved NOTCH1 expression pattern in head and neck squamous cell carcinoma is associated with NOTCH1 mutation HPV status and high-risk features

机译:头颈部鳞状细胞癌中破切的NOTCH1表达模式与NOTCH1突变HPV状态和高危特征有关

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摘要

The Notch pathway is frequently altered in HNSCCs, however the clinical significance of NOTCH1 dysregulation is poorly understood. This study was designed to characterize expression of the transcriptionally active NOTCH1 Intracellular Domain (NICD1) in HNSCCs and evaluate its association with NOTCH1 mutation status and clinical parameters. Immunohistochemistry for NICD1 was performed on 79 previously sequenced archival HNSCCs with known NOTCH1 mutation status. Three distinct immunohistochemical staining patterns were identified: positive/peripheral (47%), positiveon-peripheral (34%) and negative (19%). NICD1 expression was associated with NOTCH1 mutation status (p<0.001). Most NOTCH1-wild type tumors were peripheral (55%), while mutated NOTCH1 tumors were most commonly negative (47%). Non-peripheral tumors were more likely than peripheral tumors to have extracapsular spread (aOR 16.01, 95% CI=1.92–133.46, p=0.010) and poor differentiation (aOR 5.27, 95% CI=0.90–30.86, p=0.066). Negative staining tumors tended to be poorly differentiated (aOR 24.71, 95% CI=1.53–399.33, p=0.024) and were less likely to be HPV-positive (aOR 0.043, 95% CI=0.001–1.59, p=0.087). NOTCH1 mutagenesis was significantly associated with HPV status, with NOTCH1-wild-type tumors more likely to be HPV-positive than NOTCH1-mutated tumors (aOR 19.06, 95% CI=1.31–276.15, p=0.031). TP53 disruptive mutations were not associated with NICD1 expression or NOTCH1 mutation. In conclusion, NICD1 is expressed in three distinct patterns in HNSCC that are significantly associated with high-risk features. These findings further support a dual role for NOTCH1 as both tumor suppressor and oncogene in HNSCC. Further research is necessary to clarify the role of NOTCH1 in HNSCC and understand the clinical and therapeutic implications therein.
机译:在HNSCC中,Notch通路经常发生改变,但是对NOTCH1失调的临床意义了解甚少。本研究旨在表征HNSCC中转录活性NOTCH1胞内域(NICD1)的表达,并评估其与NOTCH1突变状态和临床参数的关系。对NICD1的免疫组织化学是对79例先前测序的,具有已知NOTCH1突变状态的HNSCC进行的。鉴定出三种不同的免疫组织化学染色模式:阳性/外周血(47%),阳性/非外周血(34%)和阴性(19%)。 NICD1表达与NOTCH1突变状态相关(p <0.001)。多数NOTCH1野生型肿瘤为周围型(55%),而突变的NOTCH1肿瘤最常见为阴性(47%)。非周围肿瘤比周围肿瘤更有可能发生囊外扩散(aOR 16.01,95%CI = 1.92–133.46,p = 0.010)和较差的分化(aOR 5.27,95%CI = 0.90–30.86,p = 0.066)。阴性染色肿瘤倾向于低分化(aOR 24.71,95%CI = 1.53–399.33,p = 0.024),HPV阳性的可能性较小(aOR 0.043,95%CI = 0.001–1.59,p = 0.087)。 NOTCH1诱变与HPV状态显着相关,与NOTCH1突变的肿瘤相比,NOTCH1野生型肿瘤更可能是HPV阳性(aOR 19.06,95%CI = 1.31–276.15,p = 0.031)。 TP53破坏性突变与NICD1表达或NOTCH1突变无关。总之,NICD1在HNSCC中以三种不同的模式表达,这些模式与高风险特征显着相关。这些发现进一步支持了NOTCH1在HNSCC中作为肿瘤抑制物和癌基因的双重作用。需要进一步的研究来阐明NOTCH1在HNSCC中的作用,并了解其中的临床和治疗意义。

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