Department of 'School of Allied Health Sciences', Central Research Laboratory (CRL) and Molecular Diagnostics, Datta Meghe Institute of Higher Education and Research, Sawangi (Meghe), Wardha, India.
Ann Med. 2024 Dec;56(1):2353893. doi: 10.1080/07853890.2024.2353893. Epub 2024 May 16.
One of the ailments with the greatest fatality rates in the 21st century is cancer. Globally, molecular methods are widely employed to treat cancer-related disorders, and the body of research on this subject is growing yearly. A thorough and critical summary of the data supporting molecular methods for illnesses linked to cancer is required.
In order to guide clinical practice and future research, it is important to examine and summarize the systematic reviews (SRs) that evaluate the efficacy and safety of molecular methods for disorders associated to cancer.
We developed a comprehensive search strategy to find relevant articles from electronic databases like PubMed, Google Scholar, Web of Science (WoS), or Scopus. We looked through the literature and determined which diagnostic methods in cancer genetics were particularly reliable. We used phrases like 'cancer genetics', genetic susceptibility, Hereditary cancer, cancer risk assessment, 'cancer diagnostic tools', cancer screening', biomarkers, and molecular diagnostics, reviews and meta-analyses evaluating the efficacy and safety of molecular therapies for cancer-related disorders. Research that only consider treatment modalities that don't necessitate genetic or molecular diagnostics fall under the exclusion criteria.
The results of this comprehensive review clearly demonstrate the transformative impact of molecular methods in the realm of cancer genetics.This review underscores how these technologies have empowered researchers and clinicians to identify and understand key genetic alterations that drive malignancy, ranging from point mutations to structural variations. Such insights are instrumental in pinpointing critical oncogenic drivers and potential therapeutic targets, thus opening the door for methods in precision medicine that can significantly improve patient outcomes.
The search does not specify a timeframe for publication inclusion, it may have missed recent advancements or changes in the field's landscape of molecular methods for cancer. As a result, it may not have included the most recent developments in the field.
After conducting an in-depth study on the molecular methods in cancer genetics, it is evident that these cutting-edge technologies have revolutionized the field of oncology, providing researchers and clinicians with powerful tools to unravel the complexities of cancer at the genetic level. The integration of molecular methods techniques has not only enhanced our understanding of cancer etiology, progression, and treatment response but has also opened new avenues for personalized medicine and targeted therapies, leading to improved patient outcomes.
癌症是 21 世纪死亡率最高的疾病之一。在全球范围内,分子方法被广泛用于治疗癌症相关疾病,并且该领域的研究每年都在增长。需要对支持癌症相关疾病分子方法的数据进行全面、批判性的总结。
为了指导临床实践和未来的研究,检查和总结评估与癌症相关疾病的分子方法的疗效和安全性的系统评价(SR)非常重要。
我们制定了一项全面的搜索策略,从 PubMed、Google Scholar、Web of Science(WoS)或 Scopus 等电子数据库中查找相关文章。我们查阅文献,确定了癌症遗传学中哪些诊断方法特别可靠。我们使用了“癌症遗传学”、遗传易感性、遗传性癌症、癌症风险评估、“癌症诊断工具”、癌症筛查”、生物标志物和分子诊断”等短语,以及评估癌症相关疾病分子疗法疗效和安全性的综述和荟萃分析。仅考虑不需要遗传或分子诊断的治疗方法的研究被排除在外。
这项全面综述的结果清楚地表明了分子方法在癌症遗传学领域的变革性影响。该综述强调了这些技术如何使研究人员和临床医生能够识别和理解驱动恶性肿瘤的关键遗传改变,从点突变到结构变异。这些见解对于确定关键致癌驱动因素和潜在治疗靶点至关重要,从而为精准医学方法打开了大门,这些方法可以显著改善患者的治疗效果。
搜索未指定出版物的时间范围,因此可能错过了该领域分子方法的最新进展或变化。因此,它可能不包括该领域的最新发展。
对癌症遗传学中的分子方法进行深入研究后,显然这些尖端技术已经彻底改变了肿瘤学领域,为研究人员和临床医生提供了强大的工具,可从遗传水平上揭示癌症的复杂性。分子方法技术的整合不仅增强了我们对癌症病因、进展和治疗反应的理解,还为个性化医学和靶向治疗开辟了新途径,从而改善了患者的治疗效果。