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Targeting the Seven Cancer Hallmarks by Modulation of Oxidative Stress-induced Inflammation and Immune Activation: A Radical Therapeutic Approach

机译:通过调节氧化应激诱导的炎症和免疫活化靶向七个癌症标志:根治性方法

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Cancer killed approximately 8.8 million people in 2015 globally. Furthermore, more than 27,000 Kenyans die annually from cancers, making it number three killers after infectious and cardiovascular diseases. The current therapeutic strategies are limited in their approach, therefore not effective enough to achieve complete remission. A radical multifactorial approach targeting early events in carcinogenesis is required. The purpose of this descriptive study was to review existing studies for knowledge, research gaps in the role of oxidative stress, inflammation, immune activation in carcinogenesis and cancer hallmarks, to stimulate new research ideas which can accelerate future therapeutic target discoveries. PubMed, ScienceDirect and Google scholar databases were searched using the keywords: cancer, oxidative stress, inflammation, immune activation, carcinogenesis and cancer hallmarks. Although widely recognized, little research on oxidative stress, inflammation, immune activation, as cancer therapeutic targets has been done. In addition, studies relating oxidative stress, inflammation, immune activation with cancer hallmarks, especially replicative immortality, immune evasion, and evading growth suppression are inadequate. To highlight this, out of a total of 8,680,095 hits, only 139,694 hits related to oxidative stress, inflammation, immune activation as therapeutic targets making this area a fertile ground for future research. Similarly, out of 271, 194 hits, only 4,595 were relating oxidative stress, inflammation and immune activation with replicative immortality as a cancer hallmark. Subsequently, after pearling, 129 articles that were directly relevant to the study were selected. After critical appraisal, identified studies were analyzed, results compared and presented in form of summary tables. Despite enough documented evidence of the essential role oxidative stress, inflammation, immune activation, plays in carcinogenesis, specific role in induction of cancer hallmarks, whether causal or consequence is not clear. An understanding of the early changes that marks initiation, maintenance and progression of cancer will accelerate development of future novel therapeutic targets and prevention strategies. This will have a direct impact on prevention, early diagnosis, management and treatment of cancers in Africa, thereby helping in attainment of United Nations sustainable development goal (SDG) number three.
机译:2015年,全球癌症致死约880万人。此外,每年有超过27,000名肯尼亚人死于癌症,成为继传染病和心血管病之后的第三大杀手。当前的治疗策略在其方法上受到限制,因此不足以实现完全缓解。需要一种针对癌症发生早期事件的根本性多因素方法。这项描述性研究的目的是回顾现有研究的知识,氧化应激,炎症,免疫激活在致癌作用和癌症特征中的作用方面的研究空白,以激发可加速未来治疗靶点发现的新研究思路。使用以下关键词搜索PubMed,ScienceDirect和Google Scholar数据库:癌症,氧化应激,炎症,免疫激活,致癌作用和癌症标志。尽管被广泛认可,但关于氧化应激,炎症,免疫激活作为癌症治疗靶标的研究很少。另外,关于氧化应激,炎症,具有癌症特征的免疫激活,特别是复制永生,免疫逃避和逃避生长抑制的研究还不够。为了突出这一点,在总共8,680,095个点击中,只有139,694个与氧化应激,炎症,免疫激活相关的点击作为治疗靶标,使该领域成为未来研究的沃土。同样,在271次点击,194次点击中,只有4,595次与氧化应激,炎症和免疫激活与复制永生有关,这是癌症的标志。随后,经过珍珠化处理,选择了与研究直接相关的129篇文章。经过严格评估后,对已鉴定的研究进行分析,比较结果,并以汇总表的形式呈现。尽管有足够的文献证明氧化应激,炎症,免疫激活在致癌作用中起着重要的作用,在诱导癌症的标志中起特定作用,无论是因果关系还是后果尚不清楚。对标志着癌症发生,维持和发展的早期变化的理解将加速未来新的治疗靶点和预防策略的发展。这将直接影响非洲癌症的预防,早期诊断,管理和治疗,从而有助于实现联合国可持续发展目标三。

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