نتایج جستجو برای: pten

تعداد نتایج: 9282  

2017
Michele Milella Italia Falcone Fabiana Conciatori Silvia Matteoni Andrea Sacconi Teresa De Luca Chiara Bazzichetto Vincenzo Corbo Michele Simbolo Isabella Sperduti Antonina Benfante Anais Del Curatolo Ursula Cesta Incani Federico Malusa Adriana Eramo Giovanni Sette Aldo Scarpa Marina Konopleva Michael Andreeff James Andrew McCubrey Giovanni Blandino Matilde Todaro Giorgio Stassi Ruggero De Maria Francesco Cognetti Donatella Del Bufalo Ludovica Ciuffreda

Combined MAPK/PI3K pathway inhibition represents an attractive, albeit toxic, therapeutic strategy in oncology. Since PTEN lies at the intersection of these two pathways, we investigated whether PTEN status determines the functional response to combined pathway inhibition. PTEN (gene, mRNA, and protein) status was extensively characterized in a panel of cancer cell lines and combined MEK/mTOR i...

Journal: :Development 1999
H Huang C J Potter W Tao D M Li W Brogiolo E Hafen H Sun T Xu

Mutations in the tumor suppressor gene PTEN (MMAC1/TEP1) are associated with a large number of human cancers and several autosomal-dominant disorders. Mice mutant for PTEN die at early embryonic stages and the mutant embryonic fibroblasts display decreased sensitivity to cell death. Overexpression of PTEN in different mammalian tissue culture cells affects various processes including cell proli...

2012
Christine Carico Miriam Nuño Debraj Mukherjee Adam Elramsisy Jocelynn Dantis Jethro Hu Jeremy Rudnick John S. Yu Keith L. Black Serguei I. Bannykh Chirag G. Patil

INTRODUCTION Pre-temozolomide studies demonstrated that loss of the tumor suppressor gene PTEN held independent prognostic significance in GBM patients. We investigated whether loss of PTEN predicted shorter survival in the temozolomide era. The role of PTEN in the PI3K/Akt pathway is also reviewed. METHODS Patients with histologically proven newly diagnosed GBM were identified from a retrosp...

2015
Masaaki Kusunose Naozumi Hashimoto Motohiro Kimura Ryo Ogata Daisuke Aoyama Koji Sakamoto Shinichi Miyazaki Akira Ando Norihito Omote Kazuyoshi Imaizumi Tsutomu Kawabe Yoshinori Hasegawa

Transforming growth factor β (TGFβ) causes the acquisition of epithelial-mesenchymal transition (EMT). Although the tumor suppressor gene PTEN (phosphatase and tensin homologue deleted from chromosome 10) can negatively regulate many signaling pathways activated by TGFβ, hyperactivation of these signaling pathways is observed in lung cancer cells. We recently showed that PTEN might be subject t...

Journal: :Molecular cancer research : MCR 2014
Ida Aronchik Aishwarya Kundu Jeanne G Quirit Gary L Firestone

UNLABELLED Human melanoma cells displaying distinct PTEN genotypes were used to assess the cellular role of this important tumor-suppressor protein in the antiproliferative response induced by the chemopreventative agent indole-3-carbinol (I3C), a natural indolecarbinol compound derived from the breakdown of glucobrassicin produced in cruciferous vegetables such as broccoli and Brussels sprouts...

Journal: :Molecular cancer therapeutics 2009
Yunqing Li Fadila Guessous Charles DiPierro Ying Zhang Tucker Mudrick Lauren Fuller Elizabeth Johnson Lukasz Marcinkiewicz Matthew Engelhardt Benjamin Kefas David Schiff Jin Kim Roger Abounader

The tyrosine kinase receptor c-Met and its ligand hepatocyte growth factor (HGF) are frequently overexpressed and the tumor suppressor PTEN is often mutated in glioblastoma. Because PTEN can interact with c-Met-dependent signaling, we studied the effects of PTEN on c-Met-induced malignancy and associated molecular events and assessed the potential therapeutic value of combining PTEN restoration...

Journal: :The open endocrinology journal 2010
Ni Zeng Jennifer-Ann Bayan Lina He Bangyan Stiles

This paper describes the biological functions of PTEN and the PTEN regulated signaling pathway in pancreatic β-cells. PTEN has been shown to regulate the regeneration of β-cells. We review the pathways that are controlled by PTEN signaling and their functions in β-cell regeneration. In particular, we describe the unique effect of Pten deletion in β-cells. Unlike its effect in other tissues, Pte...

Journal: :The Biochemical journal 2004
Steven M Walker Nick R Leslie Nevin M Perera Ian H Batty C Peter Downes

The PTEN (phosphatase and tensin homologue deleted on chromosome 10) tumour-suppressor protein is a phosphoinositide 3-phosphatase which antagonizes phosphoinositide 3-kinase-dependent signalling by dephosphorylating PtdIns(3,4,5)P3. Most tumour-derived point mutations of PTEN induce a loss of function, which correlates with profoundly reduced catalytic activity. However, here we characterize a...

Journal: :Carcinogenesis 2013
Xiao-Xing Kou Ting Hao Zhen Meng Yan-Heng Zhou Ye-Hua Gan

Specificity protein 1 (Sp1) is often overexpressed in cancer cells. Its binding sites are known to exist in the phosphatase and tension homolog deleted on chromosome 10 (PTEN) promoter. In this study, we hypothesized that Sp1 negatively regulates PTEN expression. We used several cell lines to determine the effects of Sp1. The results showed that Sp1 overexpression inhibited the expression and p...

Journal: :The Journal of clinical investigation 2013
Caterina Sellitto Leping Li Junyuan Gao Michael L Robinson Richard Z Lin Richard T Mathias Thomas W White

Mutations in the human phosphatase and tensin homolog (PTEN) gene cause PTEN hamartoma tumor syndrome (PHTS), which includes cataract development among its diverse clinical pathologies. Currently, it is not known whether cataract formation in PHTS patients is secondary to other systemic problems, or the result of the loss of a critical function of PTEN within the lens. We generated a mouse line...

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