4.8 Article

Cancer Evo-Dev: A Theory of Inflammation-Induced Oncogenesis

Journal

FRONTIERS IN IMMUNOLOGY
Volume 12, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fimmu.2021.768098

Keywords

cancer; evolution; inflammation; mutation; viral infection

Categories

Funding

  1. National Key Basic Research Program of China [2015CB554006]
  2. National Natural Science Foundation of China [91529305, 81520108021, 81673250, 81521091, 82003538]
  3. Shanghai Yangfan Program [20YF1458800]

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Chronic inflammation plays a key role in cancer development by interacting with genetic predispositions, environmental exposures, and inflammation-related carcinogenic factors. Interventions that reduce inflammation levels, such as exercising and anti-inflammatory medications, can lower the risk of cancer occurrence and recurrence. The Cancer Evo-Dev theory helps understand how inflammation promotes cancer development and provides a foundation for effective prophylaxis and targeted therapy of various cancers.
Chronic inflammation is a prerequisite for the development of cancers. Here, we present the framework of a novel theory termed as Cancer Evolution-Development (Cancer Evo-Dev) 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 via 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 via 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 via 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. Cancer Evo-Dev 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.

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