| Literature DB >> 28943967 |
Xiaoping Yi1,2, Hongyan Zai3, Xueying Long1, Xiaoyi Wang1, Wenzheng Li1, Yixiong Li3.
Abstract
Pancreatic cancer (PC) is one of the most aggressive types of cancer with an extremely poor prognosis. Invasive growth and early metastasis is one of the greatest challenges to overcome for the treatment of PC. Numerous previous studies have indicated that the transcription factor Krüppel-like factor 8 (KLF8) and nuclear cofactor four and a half LIM-only protein 2 (FHL2) serve important roles in tumorigenesis and tumor progression; however, their roles in PC remain elusive. The present study revealed that KLF8 and FHL2 expression is aberrantly co-overexpressed in PC tissue samples and associated with tumor metastasis. Furthermore, a positive correlation between the expression levels of KLF8 and FHL2 was observed. Subsequently, the present study identified KLF8 as a critical inducer of epithelial-to-mesenchymal transition (EMT) and invasion. Of note, the present study demonstrated that KLF8 overexpression induced a strong increase in FHL2 expression, and subsequent promoter reporter assays determined that KLF8 directly bound and activated the FHL2 gene promoter. Furthermore, FHL2 knockdown in KLF8-overexpressing cells partially reversed the EMT and invasive phenotypes. The present study identified KLF8-induced FHL2 activation as a novel and critical signaling mechanism underlying human PC invasion.Entities:
Keywords: Krüppel-like factor 8; epithelial-to-mesanchymal transition; four and a half LIM-only protein 2; invasion; pancreatic cancer
Year: 2017 PMID: 28943967 PMCID: PMC5594250 DOI: 10.3892/ol.2017.6734
Source DB: PubMed Journal: Oncol Lett ISSN: 1792-1074 Impact factor: 2.967