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非小细胞肺癌EGFR、KRAS、ALK基因突变与不同转移器官分布的相关性研究进展

Lung cancer is the leading cause of morbidity and mortality of malignant diseases in China. Approximately 57% lung cancer patients harbored distant metastases at initial diagnosis which is relevant to poor outcomes. The research strategy of anti-lung cancer metastasis now has became the new treatmen...

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Detalles Bibliográficos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 中国肺癌杂志编辑部 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6058661/
https://www.ncbi.nlm.nih.gov/pubmed/30037374
http://dx.doi.org/10.3779/j.issn.1009-3419.2018.07.06
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collection PubMed
description Lung cancer is the leading cause of morbidity and mortality of malignant diseases in China. Approximately 57% lung cancer patients harbored distant metastases at initial diagnosis which is relevant to poor outcomes. The research strategy of anti-lung cancer metastasis now has became the new treatment directions and thoughts for lung cancer treatment. Previous studies have shown that changes in the corresponding driving genes on different signaling pathways may be related to the transfer of different organs, and the biological alteration of tumor to some extent can affect the metastatic behavior and metastatic pattern of tumor. However, current clinical and basic studies have not elucidated the molecular mechanism of the specific distant organ metastasis in the pathway of lung cancer related signal transduction, clinical research on the correlation between gene mutation and organ transfer specificity is also relatively rare. This review aims to summarize the characteristics of the expression of epidermal growth factor receptor (EGFR), anaplastic lymphoma kinase (ALK), V-Ki-ras2 Kirsten rat sarcoma viral oncogene homologue (KRAS) in non-small cell lung cancer, and the correlation between the distribution of metastatic organs.
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spelling pubmed-60586612018-08-23 非小细胞肺癌EGFR、KRAS、ALK基因突变与不同转移器官分布的相关性研究进展 Zhongguo Fei Ai Za Zhi 综述 Lung cancer is the leading cause of morbidity and mortality of malignant diseases in China. Approximately 57% lung cancer patients harbored distant metastases at initial diagnosis which is relevant to poor outcomes. The research strategy of anti-lung cancer metastasis now has became the new treatment directions and thoughts for lung cancer treatment. Previous studies have shown that changes in the corresponding driving genes on different signaling pathways may be related to the transfer of different organs, and the biological alteration of tumor to some extent can affect the metastatic behavior and metastatic pattern of tumor. However, current clinical and basic studies have not elucidated the molecular mechanism of the specific distant organ metastasis in the pathway of lung cancer related signal transduction, clinical research on the correlation between gene mutation and organ transfer specificity is also relatively rare. This review aims to summarize the characteristics of the expression of epidermal growth factor receptor (EGFR), anaplastic lymphoma kinase (ALK), V-Ki-ras2 Kirsten rat sarcoma viral oncogene homologue (KRAS) in non-small cell lung cancer, and the correlation between the distribution of metastatic organs. 中国肺癌杂志编辑部 2018-07-20 /pmc/articles/PMC6058661/ /pubmed/30037374 http://dx.doi.org/10.3779/j.issn.1009-3419.2018.07.06 Text en 版权所有©《中国肺癌杂志》编辑部2018 https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed in accordance with the terms of the Creative Commons Attribution (CC BY 3.0) License. See: https://creativecommons.org/licenses/by/3.0/
spellingShingle 综述
非小细胞肺癌EGFR、KRAS、ALK基因突变与不同转移器官分布的相关性研究进展
title 非小细胞肺癌EGFR、KRAS、ALK基因突变与不同转移器官分布的相关性研究进展
title_full 非小细胞肺癌EGFR、KRAS、ALK基因突变与不同转移器官分布的相关性研究进展
title_fullStr 非小细胞肺癌EGFR、KRAS、ALK基因突变与不同转移器官分布的相关性研究进展
title_full_unstemmed 非小细胞肺癌EGFR、KRAS、ALK基因突变与不同转移器官分布的相关性研究进展
title_short 非小细胞肺癌EGFR、KRAS、ALK基因突变与不同转移器官分布的相关性研究进展
title_sort 非小细胞肺癌egfr、kras、alk基因突变与不同转移器官分布的相关性研究进展
topic 综述
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6058661/
https://www.ncbi.nlm.nih.gov/pubmed/30037374
http://dx.doi.org/10.3779/j.issn.1009-3419.2018.07.06
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