Editorial
Copyright ©2010 Baishideng Publishing Group Co.
World J Gastroenterol. Nov 21, 2010; 16(43): 5395-5404
Published online Nov 21, 2010. doi: 10.3748/wjg.v16.i43.5395
Table 2 Bacterial toxins and their possible roles in carcinogenesis
ToxinSourceActivity and outcome
Potential genotoxins
CDT (three subunits: CdtB is a functional unit, while CdtA and CdtC serve as accessory units for delivery into target cells)Haemophilus ducreyi, Helicobacter hepaticus, Salmonella typhi. Actinobacillus actinomycetemcomitansDNAase; DNA damage and cell cycle inhibitor[56,57]
Cytolethal distending toxin BSalmonella typhiDNAase activity, genotoxic by creating DNA lesions[58]
ColibactinEscherichia coliMechanism unknown[59]
Potential pro-carcinogenic toxins
Pasturella multocida toxinPasturella multocidaModifies Gq proliferation[60]
CagAHelicobacter pyloriBinds to SHP2 and c- Met cells scattering[61]
Vacuolating cytotoxin AHelicobacter pyloriUpregulation of VEGF expression (seems to depend on the activation of EGFR, MAP kinase and COX-2 mediated)
Bacteroides fragilis toxinBacteroides fragilisCleaves E- cadherin proliferation[62]
Cytotoxic necrotizing factor-1Escherichia coli, Shigella dysenteriae, Campylobacter jejuni and Salmonella typhi, Helicobacter hepaticus, Actinobacillus actinomycetemcomitansModifies Rho family proteins, inflammation and inhibition of cell cycle, blocks cytokines[39]
Cycle inhibiting factorEscherichia coliInhibit cell cycle at G2-M transition[63]
MAPCitrobacter rodentiumMultifunctional effectors protein that target host cell mitochondria implicated in the disruption of epithelial barrier function both in vitro and in vivo[64]
VEGFBartonella speciesAngiogenesis and proliferation[65]