نتایج جستجو برای: alk kinase

تعداد نتایج: 231548  

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2015
Greg Lemke

RTKs and Their Ligands Aberrant, uncontrolled activation of receptor tyrosine kinases (RTKs) is the “original sin” of many human cancers, in that this activation can both initiate and drive the evolution of tumors (1). Mutation and overexpression of the multiple members of the epidermal growth factor/ErbB receptor family, to cite only a single example, constitute cancer drivers that have been c...

2016
Shunpei Satoh Atsushi Takatori Atsushi Ogura Kenichi Kohashi Ryota Souzaki Yoshiaki Kinoshita Tomoaki Taguchi Md. Shamim Hossain Miki Ohira Yohko Nakamura Akira Nakagawara

In neuroblastoma (NB), one of the most common paediatric solid tumours, activation of anaplastic lymphoma kinase (ALK) is often associated with poor outcomes. Although genetic studies have identified copy number alteration and nonsynonymous mutations of ALK, the regulatory mechanism of ALK signalling at protein levels is largely elusive. Neuronal leucine-rich repeat 1 (NLRR1) is a type 1 transm...

Journal: :Cancer immunology research 2015
Claudia Voena Matteo Menotti Cristina Mastini Filomena Di Giacomo Dario Livio Longo Barbara Castella Maria Elena Boggio Merlo Chiara Ambrogio Qi Wang Valerio Giacomo Minero Teresa Poggio Cinzia Martinengo Lucia D'Amico Elena Panizza Luca Mologni Federica Cavallo Fiorella Altruda Mohit Butaney Marzia Capelletti Giorgio Inghirami Pasi A Jänne Roberto Chiarle

Non-small cell lung cancer (NSCLC) harboring chromosomal rearrangements of the anaplastic lymphoma kinase (ALK) gene is treated with ALK tyrosine kinase inhibitors (TKI), but the treatment is successful for only a limited amount of time; most patients experience a relapse due to the development of drug resistance. Here, we show that a vaccine against ALK induced a strong and specific immune res...

Journal: :Skin 2021

Anaplastic large cell lymphomas (ALCLs) are a group of CD30 positive T-cell non-Hodgkin lymphomas, accounting for only 3% all lymphomas. As per the 2017 World Health Organization updated classification, there four variants ALCL: anaplastic lymphoma kinase (ALK) positive, ALK negative, primary cutaneous, and breast-implant associated. The different ALCL share overlapping clinical presentations p...

Journal: :Clinical cancer research : an official journal of the American Association for Cancer Research 2011
Takaaki Sasaki Pasi A Jänne

The identification of oncogenic alterations in subsets of patients with non-small cell lung cancer (NSCLC) is transforming clinical care. Genomic rearrangements in anaplastic lymphoma kinase (ALK) are detected in 3% to 7% of patients with NSCLC. The ALK tyrosine kinase inhibitor crizotinib has demonstrated clinical efficacy in ALK-rearranged NSCLC patients and was recently approved by the U.S. ...

Journal: :Clinical cancer research : an official journal of the American Association for Cancer Research 2016
Yael P Mossé

In this era of more rational therapies, substantial efforts are being made to identify optimal targets. The discovery of translocations involving the anaplastic lymphoma kinase (ALK) receptor tyrosine kinase in a subset of non-small cell lung cancers has become a paradigm for precision medicine. Notably, ALK was initially discovered as the fusion gene in anaplastic large cell non-Hodgkin lympho...

2011
Sai-Hong Ignatius Ou

Epidermal growth factor receptor (EGFR) tyrosine inhibitors were first approved for the treatment of non-small cell lung cancer (NSCLC) in 2003 in the US. Activating EGFR mutations were subsequently discovered in 2004, and heralded the era of molecular targeted therapy in NSCLC. The discovery of anaplastic lymphoma kinase (ALK) rearrangement in NSCLC in 2007 by two independent groups not only r...

2018
Geeta Geeta Sharma Ines Mota Luca Mologni Enrico Patrucco Carlo Gambacorti-Passerini Roberto Chiarle

Anaplastic lymphoma kinase (ALK) is a validated molecular target in several ALK-rearranged malignancies, particularly in non-small-cell lung cancer (NSCLC), which has generated considerable interest and effort in developing ALK tyrosine kinase inhibitors (TKI). Crizotinib was the first ALK inhibitor to receive FDA approval for ALK-positive NSCLC patients treatment. However, the clinical benefit...

2016
Ryohei Katayama Takuya Sakashita Noriko Yanagitani Hironori Ninomiya Atsushi Horiike Luc Friboulet Justin F. Gainor Noriko Motoi Akito Dobashi Seiji Sakata Yuichi Tambo Satoru Kitazono Shigeo Sato Sumie Koike A. John Iafrate Mari Mino-Kenudson Yuichi Ishikawa Alice T. Shaw Jeffrey A. Engelman Kengo Takeuchi Makoto Nishio Naoya Fujita

The anaplastic lymphoma kinase (ALK) fusion oncogene is observed in 3%-5% of non-small cell lung cancer (NSCLC). Crizotinib and ceritinib, a next-generation ALK tyrosine kinase inhibitor (TKI) active against crizotinib-refractory patients, are clinically available for the treatment of ALK-rearranged NSCLC patients, and multiple next-generation ALK-TKIs are currently under clinical evaluation. T...

Journal: :Cancer research 2010
Takaaki Sasaki Katsuhiro Okuda Wei Zheng James Butrynski Marzia Capelletti Liping Wang Nathanael S Gray Keith Wilner James G Christensen George Demetri Geoffrey I Shapiro Scott J Rodig Michael J Eck Pasi A Jänne

The ALK kinase inhibitor crizotinib (PF-02341066) is clinically effective in patients with ALK-translocated cancers, but its efficacy will ultimately be limited by acquired drug resistance. Here we report the identification of a secondary mutation in ALK, F1174L, as one cause of crizotinib resistance in a patient with an inflammatory myofibroblastic tumor (IMT) harboring a RANBP2-ALK translocat...

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