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Carcinogenic bacteria

Bacteria known or suspected to cause cancer

  • 5 min read
  • 3 chapters

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Through Bacteria, Carcinogen and Virus

Oncoviruses are viral agents that are similarly suspected of causing cancer.

Known to cause cancer

Helicobacter pylori colonizes the human stomach and duodenum. It is described as a Class 1 carcinogen. In some cases it can cause stomach cancer and MALT lymphoma. Animal models have demonstrated Koch's third and fourth postulates for the role of Helicobacter pylori in the causation of stomach cancer. The mechanism by which H. pylori causes cancer may involve chronic inflammation, or the direct action of some of its virulence factors, for example, CagA has been implicated in carcinogenesis. Another bacteria that is in this genus is Helicobacter hepaticus, which causes hepatitis and liver cancer in mice.

Chronic inflammation

Chronic inflammation contributes to the pathogenesis of several types of malignant diseases, but it is particularly important for H. pylori. Following a H. pylori infection many circulating immune cells are recruited to the infection site including neutrophils. To destroy the pathogens, neutrophils produce substances with antimicrobial activities such as oxidants like reactive oxygen species (ROS) and reactive nitrogen species (RNS). H. pylori can survive the induced oxidative stress by producing antioxidant enzymes such as e.g., catalase. However, the overproduction of ROS and RNS induces various types of DNA damage in the infected gastric cells.At the same time H. pylori is known to down-regulate major DNA repair pathways. As a result, genomic and mitochondrial mutations accumulate, leading to genomic instability - a well-known hallmark of Cancer - in the gastric cells.

CagA

The virulence factor CagA in H. pylori has been linked to the development of gastric cancer. Once CagA is injected into the cytoplasm it can change the gastric cell signaling in both a phosphorylation-dependent and -independent manner. Phosphorylated CagA affects cell adhesion, spread and migration but can also induce the release of the proinflammatory chemokine IL-8. Additionally, interactions of the CRPIA motif in non-phosphorylated CagA were shown to lead to the persistent activation of the PI3K/Akt pathway, a pathway that is often overly active in many human cancers. This leads to the activation of the pro-inflammatory NF-κB and β-catenin pathways as well as increased gastric cell proliferation. Furthermore, CagA has also been found to increase tumor suppressor gene hypermethylation and thereby inhibiting the tumor suppressor genes. This is achieved by upregulating the methyltransferase DNMT1 via the AKT–NF-κB pathway. Lastly, CagA also induces the expression of the enzyme spermine oxidase (SMOX) that converts spermine to spermidine. As a by-product H2O2 is produced which causes ROS accumulation and contributes to the oxidative stress that the gastric cells experience during chronic inflammation.

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