Zobrazeno 1 - 10
of 32
pro vyhledávání: '"MET Exon 14 Mutation"'
Autor:
François Pinquie, Alain Morel, Benjamin Morvan, Jérémy Sandrini, Olivier Molinier, Alexis B. Cortot, Camille Guguen, Louise-Marie Chevalier
Publikováno v:
Clinical Lung Cancer. 23:e131-e134
Clinical Practice Points • What is already known about this subject? • Resistance mechanisms to osimertinib in T790M positive NSCLC patients are multiple and heterogeneous, combining de novo EGFR alterations (C797S mutation), EGFR-independent mec
Publikováno v:
Expert Opinion on Therapeutic Targets. 25:249-268
Introduction: The MET gene and its pathway normally plays a crucial role in cell homeostasis, motility, and apoptosis. However, when the MET gene is altered, there is an imbalance toward cell proli...
Autor:
Alexandr O. Ivantsov, Natalia V. Mitiushkina, Tatiana N. Sokolova, Maxim M. Kholmatov, Ilya A. Stepanov, Vladislav I. Tiurin, Ekatherina Sh. Kuligina, Olga S. Yatsuk, Alexandr A. Romanko, Alexandr V. Togo, Alexey M. Belyaev, Evgeny N. Imyanitov
Publikováno v:
Biochimie. 165:267-274
MET exon 14 skipping (exon 14Δ) mutations are associated with tumor sensitivity to a number of tyrosine kinase inhibitors, however clinical testing for MET gene status remains complicated. We developed a simple allele-specific PCR cDNA-based test, w
Publikováno v:
OncoTargets and Therapy. 12:7323-7328
Background Pulmonary sarcomatoid carcinoma (PSC) is a rare and poorly differentiated type of non-small cell lung cancer (NSCLC) with specific characteristics, which usually presents a challenge in clinical practice. Mesenchymal-epithelial transition
Autor:
Ruo-Yan Qin, Ling-Yue Zhang, Cheng-Hua Lu, Ling-Shuang Liu, Xiao-Yan Guo, Hong-Hao Xue, Hui-Yong Zhang, Xin-Bei Yuan
Publikováno v:
Medicine
Rationale: Lung cancer is a leading cause of cancer-related mortality worldwide. Currently, targeted therapy has proved highly efficient in the treatment of advanced non-small cell lung cancer (NSCLC). Mesenchymal-epithelial transition factor (MET) i
Autor:
Jan Braess, Frank Ueckeroth, Diana S.Y. Abdulla, Carina Heydt, Anna-Kristina Eisert, Frank Beckers, Wolfram Meister, Hans-Joachim Kabitz, Johann Lorenzen, Monika Serke, Sabine Merkelbach-Bruse, Sebastian Michels, Jana Fassunke, Florian Kron, A. Meyer, Gabriele Wessling, Lucia Nogova, Bernhard Schaaf, Juliane Sueptitz, Matthias Scheffler, Carsten Schaepers, Sophia Koleczko, Reinhard Buettner, Clemens Schulte, Britta Kaminsky, Richard F. Riedel, Anna Kron, Stefan Krueger, Wolfgang Schulte, Joachim Lorenz, Michael Hamm, Kato Kambartel, Anne M. Schultheis, Christian Grohé, Jürgen Wolf, Lea Ruge, Jutta Kappes, Jens Panse, Niels Reinmuth, Rieke Fischer
Publikováno v:
Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer. 16(4)
Robust data on the outcome of MET-aberrant NSCLC with nontargeted therapies are limited, especially in consideration of the heterogeneity of MET-amplified tumors (METamp).A total of 337 tumor specimens of patients with MET-altered Union for Internati
Autor:
Tong-Tong Zhang, Puyuan Xing, Bingning Wang, Lei Guo, Xiuyun Liu, Lixia Chu, Yan Li, Weihua Li, Tian Qiu, Wenting Huang, Jianming Ying, Junling Li
Publikováno v:
Clinical Lung Cancer. 19:e391-e398
Background The MET gene has been recognized as a potential important therapeutic target in non–small-cell lung cancer (NSCLC). We sought to investigate the MET exon 14 mutations in a cohort of Chinese patients with NSCLC. Methods We tested 461 NSCL
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Autor:
Si-Yang Liu, Qing Zhou, Xu-Chao Zhang, Hong-Fei Gao, Lan-Ying Gou, Yi-Long Wu, Zhong-Yi Dong, Wen-Zhao Zhong, Yang Shao, A. Li, Jian Su, Jin-Ji Yang, Na-Na Lou
Publikováno v:
Journal of Thoracic Oncology. 11:1503-1510
Predictive biomarkers of mesenchymal-to-epithelial transition factor (MET)-targeted therapy remain elusive. Since the discovery of the MNNG HOS Transforming gene (MET) exon 14 mutation, it has been found to have the best potential to become one preci
Publikováno v:
Translational Cancer Research. 5:S101-S105
In their recent work published in the Journal of Clinical Oncology, Awad and colleagues presented the interesting results of next-generation sequencing analysis conducted on tissue from 6,376 cancer patients, with a special focus on the description o