Department of Interventional Radiology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, China.
Department of Colorectal Surgery, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, China.
Cancer Med. 2024 Jul;13(14):e70041. doi: 10.1002/cam4.70041.
Colorectal cancer (CRC) is among the most hackneyed malignancies. Even patients with identical clinical symptoms and the same TNM stage still exhibit radically different clinical outcomes after receiving equivalent treatment regimens, indicating extensive heterogeneity of CRC. Myriad molecular subtypes of CRC have been exploited for decades, including the most compelling consensus molecular subtype (CMS) classification that has been broadly applied for patient stratification and biomarker-drug combination formulation. Encountering barriers to clinical translation, however, CMS classification fails to fully reflect inter- or intra-tumor heterogeneity of CRC. As a consequence, addressing heterogeneity and precisely managing CRC patients with unique characteristics remain arduous tasks for clinicians.
In this review, we systematically summarize molecular subtypes of CRC and further elaborate on their clinical applications, limitations, and future orientations.
In recent years, exploration of subtypes through cell lines, animal models, patient-derived xenografts (PDXs), organoids, and clinical trials contributes to refining biological insights and unraveling subtype-specific therapies in CRC. Therapeutic interventions including nanotechnology, clustered regulatory interspaced short palindromic repeat/CRISPR-associated nuclease 9 (CRISPR/Cas9), gut microbiome, and liquid biopsy are powerful tools with the possibility to shift the immunologic landscape and outlook for CRC precise medicine.
结直肠癌(CRC)是最常见的恶性肿瘤之一。即使患者具有相同的临床症状和相同的 TNM 分期,在接受相同的治疗方案后仍表现出截然不同的临床结局,这表明 CRC 存在广泛的异质性。CRC 已经存在数十年的众多分子亚型,包括最引人注目的共识分子亚型(CMS)分类,该分类已广泛应用于患者分层和生物标志物-药物联合制剂的制定。然而,CMS 分类在临床转化中遇到了障碍,无法完全反映 CRC 的肿瘤内或肿瘤间异质性。因此,解决CRC 的异质性并精确管理具有独特特征的患者仍然是临床医生的艰巨任务。
在这篇综述中,我们系统地总结了 CRC 的分子亚型,并进一步阐述了它们的临床应用、局限性和未来方向。
近年来,通过细胞系、动物模型、患者来源的异种移植物(PDX)、类器官和临床试验对亚型的探索有助于深化生物学见解,并揭示 CRC 中的亚型特异性治疗方法。包括纳米技术、成簇规律间隔短回文重复/CRISPR 相关核酸酶 9(CRISPR/Cas9)、肠道微生物组和液体活检在内的治疗干预措施是强大的工具,有可能改变 CRC 精准医学的免疫景观和前景。