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Carcinogenesis
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Carcinogenesis

Multistep model of carcinogenesis
Cancers arise from the stepwise accumulation of mutations.
    • Initiation, Promotion, & Progression
Cancer development depends on predisposing and environmental factors, age, and other influences; furthermore, these variables have synergistic effects (for example, it appears that alcohol and tobacco act together to increase risk of certain cancers).
Genetic Factors:
Genetic mutations:
Some mutations lead to loss-of-function in tumor suppressor genes; for example, a dysfunctional APC gene is associated with colon cancer.
Mutations can also lead to oncogenic gain-of-function or gene amplification. For example, translocation and subsequent amplification of the MYC oncogene is associated with Burkitt Lymphoma.
Acquired predisposing factors:
Chronic infection and inflammation promotes increased cell turnover, metaplasia, and other pre-cancer events; for example, infection by Helicobacter pylori and the ensuing inflammation can lead to gastric cancer.
Immunodeficiencies leave patients more susceptible to cancers caused by oncogenic viruses; for example, lymphomas are associated with deficiencies in T-cell immunity.
Precursor lesions can progress to cancer in some cases. Such lesions may be detectable in screenings, and early treatment may reduce the risk that they progress to cancer.
Examples of precursor lesions:
Bronchial mucosa: Inflammatory metaplasia in the bronchial mucosa; this can occur as the result of smoking. Learn more about lung cancer.
Endoemtrium: Non-inflammatory hyperplasia of the endometrium, which is result of continuous estrogen stimulation. Learn more about uterine cancer.
Colon: Villous adenomas, which are benign neoplasms in the colon; unlike most other benign neoplasms, villous adenomas progress to cancer in about 50% of cases.
Learn more about colon cancer.
Initiation, Promotion, & Progression
INITIATION
Initiation occurs when the first driver mutation induces permanent non-lethal DNA damage to a cell.
    • Because the first driver mutation initiates the process of carcinogenesis, the agents responsible are called "initiators":
Characteristics of initiating agents: They are carcinogens Produce electrophiles (electron-deficient atoms that react with DNA, RNA, and proteins) Bind DNA to form adducts Mutagens Initiating actions are irreversible Activities are additive.
Carcinogens can be chemical, microbial, or physical.
Chemical initiators Most common initiators, comprising about 90% of all carcinogens; they can be indirect-acting or direct-acting.
Indirect-acting carcinogens require metabolic activation. Examples include: Polycyclic aromatic hydrocarbons (aka, PAHs), which are released by burning fossil fuels and tobacco; Aflatoxin B1, which is naturally produced by Aspergillus fungi; and, Benzidine, which is a synthetic chemical formerly used to produce dyes; because it is a known carcinogen, it is no longer sold in the U.S.
Direct-acting chemical carcinogens do not require metabolic activation. Paradoxically, some anticancer drugs fall into this category; Other examples include: dimethyl sulfate, which can be used as a methylating agent, and, diepoxybutane, which was formerly used in industrial settings.
Microbial initiators Some strains of the human papillomavirus (HPV) that are associated with oncogenic E6 and E7 proteins.
Epstein-Barr Virus (EBV), which is associated with the African form of Burkitt Lymphoma.
Hepatitis B and C, which are associated with liver cancer.
  • Bacterium H. pylori, which is associated with gastric cancers.
Physical initiators UV rays, which are associated with squamous cell carcinoma. Other examples include electromagnetic and particulate radiations.
PROMOTION
Clonal Expansion
The promotion stage of carcinogenesis comprises clonal expansion, which occurs when promoters induce the proliferation of the DNA-damaged cell. Be aware that this can occur long after the initiation event.
Tumor Formation
As a result of clonal expansion, a tumor forms; it can be either benign or pre-neoplastic.
Promoting Agents
Characteristics of promoting agents: they do NOT produce electrophiles, nor do they bind DNA; they are not mutagens; and, their effects are usually reversible. Furthermore, their effects are modulated by diet, hormonal and environmental factors. Promoters act as mitogens; that is, they promote cell division. Some agents can act as both initiators AND promoters.
Examples of promoters include: hormones and growth factors; phorbol esters; and products of chronic inflammation.
ADDITIONAL DRIVER MUTATIONS
Continued proliferation exposes pre-neoplastic cells to additional driver mutations.
These 80+ mutations lead to the acquisition of defining cancer hallmarks, which include:
  • Self-sufficiency and the ability to ignore growth suppressors
  • Evasion of apoptosis and immortality
  • Altered metabolism and angiogenesis to meet nutritional needs
  • Iinvasion and metastasis into new niches; and, evasion of the host immune system.
This process can take years, even decades, and helps account for the latent period it takes for some cancers to develop.
PROGRESSION
Progression comprises genetic evolution and selection for aggressive cancer cell phenotypes ultimately produces a malignant tumor.
Unlike the benign tumor we drew in the promotion stage, this malignant tumor is genetically heterogeneous.
Common cancer sites:
Female breast Prostate Lungs and bronchi Colon and rectum Uterus, Melanomas of the skin Urinary bladder Non-Hodgkin lymphoma Kidney Thyroid Gland

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