Fatfat Zaynab, Hussein Marwa, Fatfat Maamoun, Gali-Muhtasib Hala
Department of Biology, American University of Beirut, Beirut, Lebanon.
Department of Biological Sciences, Faculty of Science, Beirut Arab University, Beirut, Lebanon.
Mol Cells. 2025 May;48(5):100200. doi: 10.1016/j.mocell.2025.100200. Epub 2025 Feb 28.
Colorectal cancer (CRC) continues to rank among the deadliest and most prevalent cancers worldwide, necessitating an innovative and comprehensive approach that addresses this serious health challenge at various stages, from screening and diagnosis to treatment and prognosis. As CRC research progresses, the adoption of an omics-centered approach holds transformative potential to revolutionize the management of this disease. Advances in omics technologies encompassing genomics, transcriptomics, proteomics, metabolomics, and epigenomics allow to unravel the oncogenic alterations at these levels, elucidating the intricacies and the heterogeneous nature of CRC. By providing a comprehensive molecular landscape of CRC, omics technologies enable the discovery of potential biomarkers for early non-invasive detection of CRC, definition of CRC subtypes, prediction of its staging, prognosis, and overall survival of CRC patients. They also allow the identification of potential therapeutic targets, prediction of drug response, tracking treatment efficacy, detection of residual disease and cancer relapse, and deciphering the mechanisms of drug resistance. Moreover, they allow the distinction of non-metastatic CRC patients from metastatic ones as well as the stratification of metastatic risk. Importantly, omics technologies open up new opportunities to establish molecular-based criteria to guide the selection of effective treatment paving the way for the personalization of therapy for CRC patients. This review consolidates current knowledge on the omics-based preclinical discoveries in CRC research emphasizing the significant potential of these technologies to improve CRC screening, diagnosis, and prognosis and promote the implementation of personalized medicine to ultimately reduce CRC prevalence and mortality.
结直肠癌(CRC)在全球范围内仍然是最致命、最常见的癌症之一,因此需要一种创新且全面的方法,在从筛查、诊断到治疗和预后的各个阶段应对这一严峻的健康挑战。随着CRC研究的进展,采用以组学为中心的方法具有变革潜力,能够彻底改变这种疾病的管理方式。涵盖基因组学、转录组学、蛋白质组学、代谢组学和表观基因组学的组学技术进展,使得人们能够在这些层面揭示致癌改变,阐明CRC的复杂性和异质性。通过提供CRC的全面分子图谱,组学技术能够发现用于早期非侵入性检测CRC的潜在生物标志物,定义CRC亚型,预测其分期、预后以及CRC患者的总生存期。它们还能识别潜在的治疗靶点,预测药物反应,追踪治疗效果,检测残留疾病和癌症复发,以及破解耐药机制。此外,它们能够区分非转移性CRC患者和转移性患者,并对转移风险进行分层。重要的是,组学技术为建立基于分子的标准开辟了新机会,以指导有效治疗的选择,为CRC患者的个性化治疗铺平道路。本综述整合了关于CRC研究中基于组学的临床前发现的现有知识,强调了这些技术在改善CRC筛查、诊断和预后以及促进个性化医疗实施方面的巨大潜力,最终降低CRC的患病率和死亡率。