Next-generation sequencing technology in cancer

P. Krubaa, Dr. Anand Mohan Jha, Prof Dr.Ammar A.Razzak Mahmood, Dr. Anil Kumar, D. Abraham
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Abstract

Next-generation sequencing (NGS) technology has revolutionized cancer research and treatment by enabling comprehensive analysis of genetic mutations, alterations, and expression profiles. It allows for the identification of cancer-driving mutations, helping in the development of targeted therapies. NGS provides detailed insights into tumor heterogeneity, resistance mechanisms, and clonal evolution. Its high-throughput capacity facilitates large-scale studies, improving our understanding of cancer genomics. By enabling personalized treatment plans based on individual genetic profiles, NGS holds promise for more effective and tailored cancer therapies. Early reviews on cancer genomics often lacked comprehensive coverage of emerging technologies. They missed in-depth analysis of NGS advancements, their impact on cancer research, and clinical applications. The review addresses this gap by reviving a thorough examination of NGS methods, their role in identifying genetic mutations, and their potential in personalized cancer treatment, thus providing essential insights into the evolving landscape of cancer genomics. The article covers the advancements in technology and bioinformatic approaches for NGS data analysis. It delves into NGS applications in research and diagnostics, particularly for solid cancer diagnosis. The review highlights specific cancer types, including hereditary breast cancer, melanoma, prostate cancer, thyroid cancer, lung cancer, and colorectal cancer. It explores NGS contribution in understanding the genetic basis of these cancers and its potential for enhancing personalized diagnosis and treatment strategies. This review rectifies early lacunas by providing a comprehensive and updated examination of NGS technology, addressing gaps in previous analyses and emphasizes bioinformatic approaches for NGS data analysis, crucial for interpreting vast genomic data accurately. The review meets the current need for a thorough understanding of NGS’s role in personalized cancer treatment and research.
癌症中的新一代测序技术
下一代测序(NGS)技术可对基因突变、改变和表达谱进行全面分析,为癌症研究和治疗带来了革命性的变化。它可以识别导致癌症的基因突变,帮助开发靶向疗法。NGS 能让人详细了解肿瘤的异质性、抗药性机制和克隆进化。它的高通量能力有助于进行大规模研究,从而提高我们对癌症基因组学的认识。NGS 可根据个体基因图谱制定个性化治疗方案,有望提供更有效、更有针对性的癌症疗法。早期的癌症基因组学综述往往缺乏对新兴技术的全面覆盖。它们缺乏对 NGS 进展、其对癌症研究的影响以及临床应用的深入分析。这篇综述弥补了这一不足,重新对 NGS 方法、其在鉴定基因突变中的作用以及在个性化癌症治疗中的潜力进行了深入研究,从而为癌症基因组学不断发展的前景提供了重要见解。文章介绍了 NGS 数据分析技术和生物信息学方法的进步。文章深入探讨了 NGS 在研究和诊断中的应用,尤其是在实体癌诊断中的应用。综述重点介绍了特定的癌症类型,包括遗传性乳腺癌、黑色素瘤、前列腺癌、甲状腺癌、肺癌和结直肠癌。它探讨了 NGS 在了解这些癌症的遗传基础方面的贡献,以及其在加强个性化诊断和治疗策略方面的潜力。本综述对 NGS 技术进行了全面、最新的研究,弥补了早期研究的不足,并强调了 NGS 数据分析的生物信息学方法,这对准确解读大量基因组数据至关重要。该综述满足了当前全面了解 NGS 在个性化癌症治疗和研究中的作用的需要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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