2015
DOI: 10.1016/j.anndiagpath.2015.03.009
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Achaete-scute homolog 1 expression closely correlates with endocrine phenotype and degree of differentiation in sinonasal neuroendocrine tumors

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Cited by 14 publications
(9 citation statements)
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“…Although it is clear that the diagnosis of these 2 rare entities is an evolving situation, the advent of modern molecular biology may soon lead to improved diagnostic testing, with the real possibility that both NEC and SNUC may be recognised as a variety of closely related but new pathological entities . Separate from the histological and molecular biological advances, improvements in imaging, specifically CT–positron emission tomography (PET), may also soon be able to reliably differentiate SNUC from other sinonasal tumors …”
Section: Sinonasal Malignanciesmentioning
confidence: 99%
“…Although it is clear that the diagnosis of these 2 rare entities is an evolving situation, the advent of modern molecular biology may soon lead to improved diagnostic testing, with the real possibility that both NEC and SNUC may be recognised as a variety of closely related but new pathological entities . Separate from the histological and molecular biological advances, improvements in imaging, specifically CT–positron emission tomography (PET), may also soon be able to reliably differentiate SNUC from other sinonasal tumors …”
Section: Sinonasal Malignanciesmentioning
confidence: 99%
“…Additionally, hASH1 is responsible for neuroendocrine differentiation [16]. A recent study by Taggart et al has confirmed ONB as well as other sinonasal neuroendocrine tumors (sinonasal neuroendocrine carcinoma, sinonasal undifferentiated carcinoma) as expressing hASH1 [17]. Its expression levels positively correlate with the grade of the tumor.…”
Section: Molecular Pathogenesismentioning
confidence: 99%
“…An integrated molecular and phenotypic analysis of 52 skull base tumors confirmed expression of ASH1/ASCL1 by RT-PCR in small cell NEC, sinonasal undifferentiated carcinoma, and ONB [50]. A follow-up validation of ASH1 at the protein level in primary sinonasal tumors found ASH-1 immunoreactivity to correlate with the degree of neuroendocrine tumor differentiation [51]. High-grade neuroendocrine tumors show higher ASH1 expression, in support of previous reports indicating that expression of ASH1 appears to be restricted to immature cells [51].…”
Section: Molecular Pathogenesismentioning
confidence: 78%