| Literature DB >> 29876935 |
Masafumi Horie1,2,3, Naoya Miyashita1, Johanna Sofia Margareta Mattsson4, Yu Mikami1, Martin Sandelin4, Hans Brunnström5, Patrick Micke4, Takahide Nagase1, Akira Saito1,2.
Abstract
Small cell lung cancer (SCLC) is a neuroendocrine tumour that exhibits rapid growth and metastatic spread. Although SCLC represents a prototypically undifferentiated cancer type, thyroid transcription factor-1 (TTF-1, gene symbol NKX2-1), a master regulator for pulmonary epithelial cell differentiation and lung morphogenesis, is strongly upregulated in this aggressive cancer type. The aim of this study was to evaluate a functional role for TTF-1 in SCLC. We demonstrated that achaete-scute complex homolog 1 (ASCL1), an essential transcription factor for neuroendocrine differentiation, positively regulated TTF-1 in SCLC cell lines. Subsequently, we described genes and microRNAs (miRNAs) that were possibly controlled by TTF-1 and identified nuclear factor IB (NFIB), a recently characterised driver of SCLC progression, as a transcriptional target of TTF-1. Our findings shine light on a regulatory axis in SCLC consisting of ASCL1/TTF-1/NFIB that potentially contributes to the tumourigenesis of SCLC.Entities:
Keywords: ASCL1; NFIB; SCLC; TTF-1; neuroendocrine differentiation
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Year: 2018 PMID: 29876935 DOI: 10.1002/path.5109
Source DB: PubMed Journal: J Pathol ISSN: 0022-3417 Impact factor: 7.996