Department of Epidemiology, Second Military Medical University, Shanghai, China.
School of Public Health, Shandong First Medical University & Shandong Academy of Medical Sciences, Tai'an, China.
Front Immunol. 2021 Nov 22;12:768098. doi: 10.3389/fimmu.2021.768098. eCollection 2021.
Chronic inflammation is a prerequisite for the development of cancers. Here, we present the framework of a novel theory termed as Cancer Evolution-Development () based on the current understanding of inflammation-related carcinogenesis, especially hepatocarcinogenesis induced by chronic infection with hepatitis B virus. The interaction between genetic predispositions and environmental exposures, such as viral infection, maintains chronic non-resolving inflammation. Pollution, metabolic syndrome, physical inactivity, ageing, and adverse psychosocial exposure also increase the risk of cancer inducing chronic low-grade smoldering inflammation. Under the microenvironment of non-resolving inflammation, pro-inflammatory factors facilitate the generation of somatic mutations and viral mutations by inducing the imbalance between the mutagenic forces such as cytidine deaminases and mutation-correcting forces including uracil-DNA glycosylase. Most cells with somatic mutations and mutated viruses are eliminated in survival competition. Only a small percentage of mutated cells survive, adapt to the hostile environment, retro-differentiate, and function as cancer-initiating cells altering signaling pathways. These cancer-initiating cells acquire stem-ness, reprogram metabolic patterns, and affect the microenvironment. The carcinogenic process follows the law of "mutation-selection-adaptation". Chronic physical activity reduces the levels of inflammation upregulating the activity and numbers of NK cells and lymphocytes and lengthening leukocyte telomere; downregulating proinflammatory cytokines including interleukin-6 and senescent lymphocytes especially in aged population. Anti-inflammation medication reduces the occurrence and recurrence of cancers. Targeting cancer stemness signaling pathways might lead to cancer eradication. not only helps understand the mechanisms by which inflammation promotes the development of cancers, but also lays the foundation for effective prophylaxis and targeted therapy of various cancers.
慢性炎症是癌症发展的前提。在这里,我们提出了一个新理论的框架,称为癌症进化-发展(Cancer Evolution-Development (CancerEvoD)),该理论基于目前对炎症相关致癌作用的理解,特别是慢性乙型肝炎病毒感染引起的肝癌发生。遗传易感性和环境暴露(如病毒感染)之间的相互作用维持着慢性未解决的炎症。污染、代谢综合征、缺乏身体活动、衰老和不良的社会心理暴露也会增加癌症风险,导致慢性低度潜伏性炎症。在未解决炎症的微环境中,促炎因子通过诱导胞嘧啶脱氨酶等诱变因子与包括尿嘧啶-DNA 糖苷酶在内的突变校正因子之间的失衡,促进体细胞突变和病毒突变的产生。大多数具有体细胞突变和突变病毒的细胞在生存竞争中被淘汰。只有一小部分突变细胞存活下来,适应恶劣的环境,逆行分化,并作为癌症起始细胞改变信号通路。这些癌症起始细胞获得干细胞特性,重新编程代谢模式,并影响微环境。致癌过程遵循“突变-选择-适应”的规律。慢性体力活动可降低炎症水平,上调 NK 细胞和淋巴细胞的活性和数量,延长白细胞端粒;下调包括白细胞介素 6 在内的促炎细胞因子和衰老的淋巴细胞,特别是在老年人群中。抗炎药物可降低癌症的发生和复发风险。靶向癌症起始细胞的信号通路可能导致癌症的根除。CancerEvoD 不仅有助于理解炎症促进癌症发展的机制,也为各种癌症的有效预防和靶向治疗奠定了基础。