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Stool testing for the early detection of pancreatic cancer: rationale and current evidence

机译:大便检查以早期发现胰腺癌:基本原理和当前证据

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The development of effective tools for the early detection of pancreatic cancer, or its precursors,nin high-risk subjects could play a key role in reducing the burden of this disease, which is thenmost lethal among solid gastrointestinal tumors. Given the poor accessibility of the pancreasndue to its anatomic site, and given the limitations of imaging modalities, biomarker screeningnmight be a promising diagnostic option. This review focuses on the rationale of using stoolnmarkers for the early detection of pancreatic cancer, and systematically summarizes currentnevidence. Despite several potential advantages of stool testing for pancreatic cancer and itsnbiological plausibility, only six studies investigating two genetic markers in stool (the K-ras andnthe p53 gene) could be identified. Even though these studies were limited in size and couldnhardly approximate the screening setting, both markers appear to lack sensitivity and, innparticular, specificity. The investigation of further marker candidates (e.g., epigenetic markers)nin adequately designed studies represents an important next step to explore the potential ofnstool testing for pancreatic cancer. Pertinent studies could greatly benefit from recentnmethodological advances gained in connection with stool testing for colorectal cancer.
机译:在高危人群中,开发用于早期检测胰腺癌或其前体的有效工具可能在减轻这种疾病的负担中起关键作用,而这种疾病在实体胃肠道肿瘤中最为致命。鉴于胰腺到其解剖部位的可及性差,并且由于成像方式的局限性,生物标志物筛选可能是一种有前途的诊断选择。这篇评论集中在使用胰腺癌早期检测使用标记物的原理,并系统地总结当前的证据。尽管粪便检测对于胰腺癌及其生物学学可行性具有若干潜在的优势,但只有六项研究调查了粪便中的两个遗传标记(K-ras和nthe p53基因)。即使这些研究的规模有限并且几乎不能接近筛选设置,但两种标记物似乎都缺乏敏感性,尤其是特异性。在适当设计的研究中对其他标记候选项(例如表观遗传标记)的研究代表了重要的下一步,以探索工具测试胰腺癌的潜力。有关的研究可从粪便检测结直肠癌方面获得的最新方法学进展中受益匪浅。

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