Department Biochemistry, Faculty of Medicine, Medical University of Lodz, Lodz, Poland.
Roche Polska Sp. z o.o., Warsaw, Poland.
Curr Drug Targets. 2021;22(1):137-145. doi: 10.2174/1389450121666200220123844.
Colitis-associated colorectal cancer (CAC) remains a critical complication of ulcerative colitis (UC) with a mortality of approximately 15%, which makes early CAC diagnosis crucial. The current standard of surveillance, with repetitive colonoscopies and histological testing of biopsied mucosa samples, is burdensome and expensive, and therefore less invasive methods and reliable biomarkers are needed. Significant progress has been made, thanks to continuous extensive research in this field, however, no clinically relevant biomarker has been established so far. This review of the current literature presents the genetic and molecular differences between CAC and sporadic colorectal cancer and covers progress made in the early detection of CAC carcinogenesis. It focuses on biomarkers under development, which can easily be tested in samples of body fluids or breath and, once made clinically available, will help to differentiate between progressors (UC patients who will develop dysplasia) from non-progressors and enable early intervention to decrease the risk of cancer development.
结肠炎相关结直肠癌(CAC)仍然是溃疡性结肠炎(UC)的严重并发症,死亡率约为 15%,这使得早期 CAC 的诊断至关重要。目前的监测标准是反复进行结肠镜检查和活检黏膜样本的组织学检测,这种方法既繁琐又昂贵,因此需要更具侵袭性的方法和可靠的生物标志物。由于在该领域的持续广泛研究,已经取得了重大进展,但迄今为止尚未建立具有临床相关性的生物标志物。本综述介绍了 CAC 和散发性结直肠癌之间的遗传和分子差异,并涵盖了 CAC 癌变早期检测方面的进展。它重点介绍了正在开发中的生物标志物,这些标志物可以很容易地在体液或呼吸样本中进行检测,一旦在临床上可用,将有助于区分进展者(将发生异型增生的 UC 患者)和非进展者,并能够进行早期干预以降低癌症发展的风险。