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本文引用的文献

1
Identifying and Targeting the Cause of Cancer is Needed to Cure Cancer.治愈癌症需要识别并针对癌症病因。
Oncol Ther. 2016;4(1):17-33. doi: 10.1007/s40487-015-0015-6. Epub 2016 Jan 20.
2
Gemcitabine mono-therapy versus gemcitabine plus targeted therapy in advanced pancreatic cancer: a meta-analysis of randomized phase III trials.吉西他滨单药治疗与吉西他滨联合靶向治疗晚期胰腺癌:一项随机III期试验的荟萃分析
Acta Oncol. 2017 Mar;56(3):377-383. doi: 10.1080/0284186X.2017.1288922. Epub 2017 Feb 17.
3
Cancer: A disease at the crossroads of trade-offs.癌症:一种处于权衡十字路口的疾病。
Evol Appl. 2016 Dec 26;10(3):215-225. doi: 10.1111/eva.12444. eCollection 2017 Mar.
4
Somatic BRCA1/2 Recovery as a Resistance Mechanism After Exceptional Response to Poly (ADP-ribose) Polymerase Inhibition.BRCA1/2 基因种系突变与遗传性乳腺癌-卵巢癌综合征(HBOC)的发生密切相关,具有 BRCA1/2 基因种系突变的个体终生患乳腺癌和卵巢癌的风险分别为 50%~85%和 15%~40%。 **注释**:以上是对英文文本的翻译,仅供参考。
J Clin Oncol. 2017 Apr 10;35(11):1240-1249. doi: 10.1200/JCO.2016.71.3677. Epub 2017 Feb 21.
5
Tumor Microenvironment and Differential Responses to Therapy.肿瘤微环境与治疗的差异反应
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Weighted gene co-expression network analysis in identification of metastasis-related genes of lung squamous cell carcinoma based on the Cancer Genome Atlas database.基于癌症基因组图谱数据库的加权基因共表达网络分析在肺鳞状细胞癌转移相关基因鉴定中的应用
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9
Three generations of epidermal growth factor receptor tyrosine kinase inhibitors developed to revolutionize the therapy of lung cancer.为彻底改变肺癌治疗方法而研发的三代表皮生长因子受体酪氨酸激酶抑制剂。
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DNA突变可能并非癌症的病因。

DNA Mutations May Not Be the Cause of Cancer.

作者信息

Adjiri Adouda

机构信息

Physics Department, Faculty of Sciences, Sétif-1 University, Sétif, Algeria.

出版信息

Oncol Ther. 2017;5(1):85-101. doi: 10.1007/s40487-017-0047-1. Epub 2017 May 15.

DOI:10.1007/s40487-017-0047-1
PMID:28680959
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5488117/
Abstract

Cancer is the most challenging disease of our time with increasing numbers of new cases each year, worldwide. Great achievements have been reached in cancer research through deep sequencing which helped define druggable targets. However, the still-evolving targeted therapy suffers resistance suggesting that DNA mutations considered as drivers may not have a role in tumor initiation. The present work discusses the role of DNA mutations as drivers and passengers in cancer initiation and development. First, it is important to discern the role of these DNA mutations as initiating events causing cancer or as contributors crucial for the development of a tumor once it has initiated. Second, breast cancer shown here illustrates how identification of DNA mutations in cancerous cells has influenced our approach for anti-cancer drug design. The cancer trilogy we have reached and described as: initial drug; resistance/recurrence; drug/treatment combinations, calls for a paradigm shift. To design more effective cancer drugs with durable and positive outcome, future cancer research needs to move beyond the sequencing era and explore changes which are taking place in cancer cells at levels other than the DNA. Evolutionary constraints may be acting as a barrier to preserve the human species from being transformed and, for that matter, all multi-cellular species which can incur cancer. Furthermore, mutations in the DNA do occur and for a multitude of reasons but without necessarily causing cancer. New directions will draw themselves when more focus is given to the event responsible for the switch of a cell from normalcy to malignancy. Until then, targeted therapy will certainly continue to improve the outcome of patients; however, it is unlikely to eradicate breast cancer depicted here.

摘要

癌症是我们这个时代最具挑战性的疾病,全球每年新增病例数不断增加。通过深度测序在癌症研究中取得了巨大成就,这有助于确定可成药靶点。然而,仍在不断发展的靶向治疗会产生耐药性,这表明被视为驱动因素的DNA突变可能在肿瘤发生中不起作用。目前的工作讨论了DNA突变在癌症发生和发展中作为驱动因素和乘客的作用。首先,重要的是要辨别这些DNA突变是作为引发癌症的起始事件,还是作为肿瘤一旦发生后对其发展至关重要的促成因素。其次,这里展示的乳腺癌说明了癌细胞中DNA突变的鉴定如何影响了我们的抗癌药物设计方法。我们已经达到并描述为:初始药物;耐药/复发;药物/治疗组合的癌症三部曲,需要一种范式转变。为了设计出更有效的具有持久和积极效果的癌症药物,未来的癌症研究需要超越测序时代,探索癌细胞在DNA以外水平发生的变化。进化限制可能是保护人类物种不被转化的障碍,就此而言,也保护所有可能患癌症的多细胞物种。此外,DNA中的突变确实会发生,原因多种多样,但不一定会导致癌症。当更多地关注导致细胞从正常状态转变为恶性状态的事件时,新的方向将会显现出来。在此之前,靶向治疗肯定会继续改善患者的治疗效果;然而,它不太可能根除这里所描述的乳腺癌。