نتایج جستجو برای: wnt signalling and hek293t cells

تعداد نتایج: 17086001  

Journal: :Journal of cell science 2011
Karen Wallace Quan Long Emma A Fairhall Keith A Charlton Matthew C Wright

Elevated glucocorticoid levels result in the transdifferentiation of pancreatic acinar cells into hepatocytes through a process that requires a transient repression of WNT signalling upstream of the induction of C/EBP-β. However, the mechanism by which glucocorticoid interacts with WNT signalling is unknown. A screen of microarray data showed that the serine/threonine protein kinase SGK1 (serum...

2018
Gang Yang Tianyi Shen Xiaoming Yi Zhengyu Zhang Chaopeng Tang Longxin Wang Yulin Zhou Wenquan Zhou

Long non-coding RNAs (lncRNAs) are non-protein-coding transcripts in the human genome which perform crucial functions in diverse biological processes. The abnormal expression of some lncRNAs has been found in tumorigenesis, development and therapy resistance of cancers. They may act as oncogenes or tumour suppressors and can be used as diagnostic or prognostic markers, prompting their therapeut...

Journal: :Journal of cell science 2007
Vítezslav Bryja Gunnar Schulte Nina Rawal Alexandra Grahn Ernest Arenas

Previously, we have shown that Wnt-5a strongly regulates dopaminergic neuron differentiation by inducing phosphorylation of Dishevelled (Dvl). Here, we identify additional components of the Wnt-5a-Dvl pathway in dopaminergic cells. Using in vitro gain-of-function and loss-of-function approaches, we reveal that casein kinase 1 (CK1) delta and CK1epsilon are crucial for Dvl phosphorylation by non...

Journal: :Cell proliferation 2010
M-H Kim J-S Park M-S Seo J-W Jung Y-S Lee K-S Kang

OBJECTIVES One aspect of the effects of isoflavones against fat deposition might be at least associated with the mechanism by which Wnt/β-catenin signalling inhibits adipocyte differentiation. However, it remains completely unknown as to whether isoflavones might influence Wnt signalling during commitment of pluripotent mesenchymal stem cells (MSCs) to adipose lineages. In the present study, we...

2014
Marco Piva Giacomo Domenici Oihana Iriondo Miriam Rábano Bruno M Simões Valentine Comaills Inmaculada Barredo Jose A López-Ruiz Ignacio Zabalza Robert Kypta Maria d M Vivanco

Development of resistance to therapy continues to be a serious clinical problem in breast cancer management. Cancer stem/progenitor cells have been shown to play roles in resistance to chemo‐ and radiotherapy. Here, we examined their role in the development of resistance to the oestrogen receptor antagonist tamoxifen. Tamoxifen‐resistant cells were enriched for stem/progenitors and expressed hi...

2017
Eline C van Kappel Madelon M Maurice

The β-catenin destruction complex is a dynamic cytosolic multiprotein assembly that provides a key node in Wnt signalling regulation. The core components of the destruction complex comprise the scaffold proteins axin and adenomatous polyposis coli and the Ser/Thr kinases casein kinase 1 and glycogen synthase kinase 3. In unstimulated cells, the destruction complex efficiently drives degradation...

2017
Maria B. R. Piva Bastian Jakubzig Gerd Bendas

BACKGROUND integrins have been associated with the development of chemotherapy resistant tumour cells, mostly those of hematopoietic origin, by mediating the binding to the extracellular matrix. The relevance for solid tumour cells and the underlying mechanisms remain elusive. METHODS using MTT assays, we detected the loss in cisplatin sensitivity of human MV3 melanoma cells upon integrin act...

2012
Yong Jiang Xi He Philip H Howe

Canonical Wnt signalling requires caveolin-dependent internalization of low-density lipoprotein receptor-related protein 6 (LRP6). Here we report that the tumour suppressor and endocytic adaptor disabled-2 (Dab2), previously described as an inhibitor of Wnt/β-catenin signalling, selectively recruits LRP6 to the clathrin-dependent endocytic route, thereby sequestering it from caveolin-mediated e...

2014
Giovanni Zito Ichiko Saotome Zongzhi Liu Enrico G. Ferro Thomas Y. Sun Don X. Nguyen Kaya Bilguvar Christine J. Ko Valentina Greco

A fundamental goal in cancer biology is to identify the cells and signalling pathways that are keys to induce tumour regression. Here we use a spontaneously self-regressing tumour, cutaneous keratoacanthoma (KAs), to identify physiological mechanisms that drive tumour regression. By using a mouse model system that recapitulates the behaviour of human KAs, we show that self-regressing tumours sh...

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