Colorectal Research Chair, Department of Surgery, King Saud University College of Medicine, Riyadh 11472, Saudi Arabia.
Department of Biosciences, Manipal University Jaipur, Jaipur, Rajasthan 303007, India.
Int J Mol Med. 2021 Mar;47(3). doi: 10.3892/ijmm.2021.4847. Epub 2021 Jan 7.
Colorectal cancer (CRC) is the third most frequently detected type of cancer, and the second most common cause of cancer‑related mortality globally. The American Cancer Society predicted that approximately 147,950 individuals would be diagnosed with CRC, out of which 53,200 individuals would succumb to the disease in the USA alone in 2020. CRC‑related mortality ranks third among both males and females in the USA. CRC arises from 3 major pathways: i) The adenoma‑carcinoma sequence; ii) serrated pathway; and iii) the inflammatory pathway. The majority of cases of CRC are sporadic and result from risk factors, such as a sedentary lifestyle, obesity, processed diets, alcohol consumption and smoking. CRC is also a common preventable cancer. With widespread CRC screening, the incidence and mortality from CRC have decreased in developed countries. However, over the past few decades, CRC cases and mortality have been on the rise in young adults (age, <50 years). In addition, CRC cases are increasing in developing countries with a low gross domestic product (GDP) due to lifestyle changes. CRC is an etiologically heterogeneous disease classified by tumor location and alterations in global gene expression. Accumulating genetic and epigenetic perturbations and aberrations over time in tumor suppressor genes, oncogenes and DNA mismatch repair genes could be a precursor to the onset of colorectal cancer. CRC can be divided as sporadic, familial, and inherited depending on the origin of the mutation. Germline mutations in APC and MLH1 have been proven to play an etiological role, resulting in the predisposition of individuals to CRC. Genetic alterations cause the dysregulation of signaling pathways leading to drug resistance, the inhibition of apoptosis and the induction of proliferation, invasion and migration, resulting in CRC development and metastasis. Timely detection and effective precision therapies based on the present knowledge of CRC is essential for successful treatment and patient survival. The present review presents the CRC incidence, risk factors, dysregulated signaling pathways and targeted therapies.
结直肠癌(CRC)是全球第三大常见癌症,也是癌症相关死亡的第二大常见原因。美国癌症协会预测,2020 年在美国将有约 147950 人被诊断患有 CRC,其中 53200 人将死于该病。CRC 相关死亡率在美国男性和女性中均排名第三。CRC 主要有 3 种发生途径:i)腺瘤-癌序列;ii)锯齿状途径;iii)炎症途径。大多数 CRC 病例为散发性,由生活方式、肥胖、加工饮食、饮酒和吸烟等风险因素引起。CRC 也是一种常见的可预防癌症。随着 CRC 广泛筛查,发达国家 CRC 的发病率和死亡率有所下降。然而,在过去几十年中,CRC 在年轻人(年龄<50 岁)中的发病率和死亡率呈上升趋势。此外,由于生活方式的改变,低国内生产总值(GDP)的发展中国家 CRC 病例也在增加。CRC 是一种病因学异质性疾病,根据肿瘤位置和全球基因表达的改变进行分类。随着时间的推移,肿瘤抑制基因、癌基因和 DNA 错配修复基因中的遗传和表观遗传改变和异常不断积累,可能是结直肠癌发病的前兆。CRC 可根据突变来源分为散发性、家族性和遗传性。APC 和 MLH1 种系突变已被证明具有病因作用,导致个体易患 CRC。遗传改变导致信号通路失调,从而导致药物耐药性、细胞凋亡抑制和增殖、侵袭和迁移诱导,导致 CRC 发展和转移。基于目前对 CRC 的认识,及时发现和有效的精准治疗对成功治疗和患者生存至关重要。本综述介绍了 CRC 的发病率、危险因素、失调的信号通路和靶向治疗。