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Krüppel-like factors in cancer

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TLDR
The roles and regulation of the 17 known KLFs in various cancer-relevant processes are discussed, with some KLFs having different roles in normal cells and cancer, during cancer development and progression and in different cancer types.
Abstract
Kruppel-like factors (KLFs) are a family of DNA-binding transcriptional regulators with diverse and essential functions in a multitude of cellular processes, including proliferation, differentiation, migration, inflammation and pluripotency. In this Review, we discuss the roles and regulation of the 17 known KLFs in various cancer-relevant processes. Importantly, the functions of KLFs are context dependent, with some KLFs having different roles in normal cells and cancer, during cancer development and progression and in different cancer types. We also identify key questions for the field that are likely to lead to important new translational research and discoveries in cancer biology.

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Cancer-derived exosomal miR-25-3p promotes pre-metastatic niche formation by inducing vascular permeability and angiogenesis.

TL;DR: It is shown that colorectal cancer (CRC) derived exosomal miR-25-3p promotes vascular leakiness and angiogenesis, CRC metastasis, and is upregulated in CRC pateints with metastasis.
Journal ArticleDOI

Nrf2 Amplifies Oxidative Stress via Induction of Klf9

TL;DR: It is demonstrated that Klf9 independently causes increased ROS levels in various types of cultured cells and in mouse tissues and is required for pathogenesis of bleomycin-induced pulmonary fibrosis in mice and identified as a ubiquitous regulator of oxidative stress and lung injury.
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Interplay between arginine methylation and ubiquitylation regulates KLF4-mediated genome stability and carcinogenesis.

TL;DR: A critical role is pointed to for aberrant KLF4 regulation by PRMT5 in genome stability and breast carcinogenesis through structure-based modelling and simulations.
Journal ArticleDOI

Krüppel-like factors in mammalian stem cells and development

TL;DR: An overview of Krüppel-like factors, a family of zinc-finger transcription factors that play fundamental roles in development and stem cell biology, as revealed by studies of animal models is provided.
References
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Journal ArticleDOI

KLF4 suppresses transformation of pre-B cells by ABL oncogenes

TL;DR: Klf4 is identified as a putative tumor suppressor in B-cell malignancies by showing that overexpression of KLF4 induces arrest and apoptosis in the G1 phase of the cell cycle.
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Regulation of KLF4 Turnover Reveals an Unexpected Tissue-Specific Role of pVHL in Tumorigenesis

TL;DR: It is proposed that the Von Hippel-Lindau gene product, pVHL, physically interacts with KLF4 and regulates its rapid turnover observed in both differentiated and stem cells and is a facilitating factor in colorectal tumorigenesis.
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Esophageal Squamous Cell Dysplasia and Delayed Differentiation With Deletion of Krüppel-Like Factor 4 in Murine Esophagus

TL;DR: Klf4 is essential for squamous epithelial differentiation in vivo and interacts with Klf5 to maintain normal epithelial homeostasis in the adult by focusing on the squamous lined esophagus.
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Krüppel-like factor 4 functions as a tumor suppressor in cervical carcinoma.

TL;DR: The Krüppel‐like factor 4 protein, a zinc finger transcription factor that is highly expressed in epithelial tissues such as the gut and skin, has been implicated in both tumor suppression and progression and the role of KLF4 in human cervical carcinoma is still unclear.
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Up-regulation of gut-enriched krüppel-like factor by interferon-γ in human colon carcinoma cells

TL;DR: Treatment of HT‐29 cells with IFN‐γ inhibited cell proliferation and induced apoptosis, the effect was found to associate with GKLF expression suggesting that GkLF may function as a downstream target of IFN-γ.
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