摘要
非小细胞肺癌(NSCLC)是在全世界癌相关死亡最常见的原因之一。基于病人疾病的阶段,治疗选择包括手术、放射疗法及化学疗法。虽然化学疗法是晚期NSCLC主要的治疗途径,但是靶向治疗也给这群患者给予了很好的治疗机会。目前这种方法是基于临床上的基因突变的先前评估,桑格测序是指定突变状态和指引合适疗法的主要方法;然后该工具有灵敏度较低的特点。近期,新一代测序技术(NGS)已经通过增加DNA序列从大规模研究到靶向区域的可行性与可能性,引人注目地改革了癌症的分子知识。为鉴定新的靶向突变和预测耐药性的出现,本文报告了NGS作为新方法研究NSCLC的不同应用的综述,因而为该癌症的突变谱提供信息。所有研究都证明该方法有超过传统技术的一些优势。尤其是NGS能够显示低概率的基因突变并筛选出不同样品的突变形式,如活体组织切片、细胞样品及血浆循环DNA,提供了新的诊断机会。尽管在个性化治疗中有许多问题需要解决,但是NGS代表一种极具吸引力鉴定突变的系统,进而改善这个致命病人的状况。
关键词: 耐药性,基因突变景观图,新一代测序技术, NSCLC,个性化治疗,靶序列
Current Drug Targets
Title:Next Generation Sequencing in Non-Small Cell Lung Cancer: New Avenues Toward the Personalized Medicine
Volume: 16 Issue: 1
Author(s): Simona Coco, Anna Truini, Irene Vanni, Maria Giovanna Dal Bello, Angela Alama, Erika Rijavec, Carlo Genova, Giulia Barletta, Claudio Sini, Giovanni Burrafato, Federica Biello, Francesco Boccardo and Francesco Grossi
Affiliation:
关键词: 耐药性,基因突变景观图,新一代测序技术, NSCLC,个性化治疗,靶序列
摘要: Non-small cell lung cancer (NSCLC) is one of the most common causes of cancer-related death worldwide. Based on the patient’s stage of disease, treatment options include surgery, radiotherapy, and chemotherapy. Although chemotherapy remains the main therapeutic approach for advanced NSCLC, targeted therapy represents a good chance of treatment for this subgroup of patients. Currently this approach is based on previous evaluation of clinically relevant mutations and the Sanger sequencing is the main approach to assign mutational status and to guide the appropriate treatment; however this tool is characterized by a low sensitivity. Recently, the advent of next-generation sequencing (NGS) has dramatically revolutionized the molecular knowledge of cancer by increasing the feasibility and possibility to sequence DNA ranging from large scale studies to targeted regions. This review reports an overview of different applications of the NGS as novel approach to study NSCLC, thereby providing information about mutational spectrum of this cancer in order to identify novel targetable mutations and to predict the emergence of drug resistance. All studies demonstrated several advantages of this approach over the traditional tools. In particular the NGS was also able to reveal mutations in low percentage, and to screen the mutational status of different critical samples such as biopsies, cytological samples and circulating plasma DNA, offering innovative diagnostic opportunities. Despite several problems have to be overcome toward the personalized therapy, the NGS represents a highly attractive system to identify mutations improving the outcome of patients with this deadly disease.
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Simona Coco , Anna Truini , Irene Vanni , Maria Giovanna Dal Bello , Angela Alama , Erika Rijavec , Carlo Genova , Giulia Barletta , Claudio Sini , Giovanni Burrafato , Federica Biello , Francesco Boccardo and Francesco Grossi , Next Generation Sequencing in Non-Small Cell Lung Cancer: New Avenues Toward the Personalized Medicine, Current Drug Targets 2015; 16 (1) . https://dx.doi.org/10.2174/1389450116666141210094640
DOI https://dx.doi.org/10.2174/1389450116666141210094640 |
Print ISSN 1389-4501 |
Publisher Name Bentham Science Publisher |
Online ISSN 1873-5592 |
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