Das Vishal, Kalita Jatin, Pal Mintu
Biotechnology Division, CSIR-North East Institute of Science and Technology, Jorhat, Assam 785006, India.
Biotechnology Division, CSIR-North East Institute of Science and Technology, Jorhat, Assam 785006, India.
Biomed Pharmacother. 2017 Mar;87:8-19. doi: 10.1016/j.biopha.2016.12.064. Epub 2016 Dec 29.
Colorectal cancer (CRC) is one of the leading cause of cancer deaths worldwide. Since CRC is largely asymptomatic until alarm features develop to advanced stages, the implementation of the screening programme is very much essential to reduce cancer incidence and mortality rates. CRC occurs predominantly from accumulation of genetic and epigenetic changes in colon epithelial cells, which later gets transformed into adenocarcinomas.
The current challenges of screening paradigm and diagnostic ranges are from semi-invasive methods like colonoscopy to non-invasive stool-based test, have resulted in over-diagnosis and over-treatment of CRC. Hence, new screening initiatives and deep studies are required for early diagnosis of CRC. In this regard, we not only summarise current predictive and prognostic biomarkers with their potential for diagnostic and therapeutic applications, but also describe current limitations, future perspectives and challenges associated with the progression of CRC.
Currently many potential biomarkers have already been successfully translated into clinical practice eg. Fecal haemoglobin, Carcinoembryonic antigen (CEA) and CA19.9, although these are not highly promising diagnostic target for personalized medicine. So there is a critical need for reliable, minimally invasive, highly sensitive and specific genetic markers of an individualised and optimised patient treatment at the earliest disease stage possible.
Identification of a new biomarker, or a set of biomarkers to the development of a valid, and clinical sensible assay that can be served as an alternative tool for early diagnosis of CRC and open up promising new targets in therapeutic intervention strategies.
结直肠癌(CRC)是全球癌症死亡的主要原因之一。由于结直肠癌在出现警示特征发展到晚期之前大多没有症状,因此实施筛查计划对于降低癌症发病率和死亡率至关重要。结直肠癌主要源于结肠上皮细胞中遗传和表观遗传变化的积累,这些细胞随后会转变为腺癌。
目前筛查模式和诊断范围面临的挑战,从结肠镜检查等半侵入性方法到基于粪便的非侵入性检测,导致了结直肠癌的过度诊断和过度治疗。因此,需要新的筛查举措和深入研究来早期诊断结直肠癌。在这方面,我们不仅总结了当前具有诊断和治疗应用潜力的预测性和预后生物标志物,还描述了与结直肠癌进展相关的当前局限性、未来前景和挑战。
目前许多潜在的生物标志物已经成功转化为临床实践,例如粪便血红蛋白、癌胚抗原(CEA)和CA19.9,尽管这些对于个性化医疗而言并不是很有前景的诊断靶点。因此,迫切需要在疾病最早阶段获得可靠、微创、高度敏感和特异的基因标志物,以实现个体化和优化的患者治疗。
鉴定一种新的生物标志物或一组生物标志物,以开发一种有效且临床合理的检测方法,可作为结直肠癌早期诊断的替代工具,并在治疗干预策略中开辟有前景的新靶点。