Inflammation induced by cytokines has been linked to increased production of reactive oxygen species and breast cancer development. The aim of this study was to evaluate the influence COX-2, IL-1β, IL-8, and TNF-α gene expressions on DNA damage, and investigate a possible link between these factors with neoplastic process. The mRNA expression was measured by real-time PCR, and the DNA damage was analyzed by single-cell gel electrophoresis (comet assay). Our data indicated a significant increase on inflammatory gene expression in tumor tissues compared with normal tissue, and it was also associated with undifferentiated grade patients. Moreover, the results showed that the higher levels of DNA damage were observed among tumor tissue samples. Taken together, the findings presented in this study highlight the relevance of inflammation-induced oxidative stress in breast carcinogenesis.

Gastric cancer (GC) is the second leading cause of cancer-related mortality worldwide. The disease develops from the accumulation of several genetic and epigenetic changes. Among other risk factors, Helicobacter pylori infection is considered the main driving factor of GC development. H. pylori infection increases DNA damage levels and leads to epigenetic dysregulation, which may favor gastric carcinogenesis. An early step in double-strand break repair is the recruitment of ataxia-telangiectasia mutated serine/threonine kinase (ATM) to the damaged site, where it plays a key role in advancing the DNA damage checkpoint process. H. pylori infection has been associated with the introduction of double-strand breaks in epithelial cells, triggering damage signaling and repair response involving ATM. Thus, the current study analyzed the effect of H. pylori infection on the DNA damage response sensor, ATM, in gastric epithelial cells and in biopsy specimens from patients with GC. In this study, we identified that H. pylori infection stimulated DNA damage, and therefore induced ATM in a virulence factor-dependent manner. In addition, we found that H. pylori might activate ATM through histone H3 and H4 hyperacetylation and DNA promoter hypomethylation. Our findings show a mechanism associating ATM signaling induction with H. pylori infection.

A evolução no campo da genômica e áreas afins nos últimos anos vêm permitindo estudos cada vez mais detalhados do microbioma humano. O trato gastrointestinal, mais precisamente o intestino, é o local que apresenta uma maior quantidade e diversidade de microrganismos, sofrendo então grande influência para a manutenção da homeostase, deste modo, nessa revisão procuramos resumir literaturas recentes sobre o microbioma intestinal e evidência de como sua composição no hospedeiro pode influenciar o seu metabolismo e a ocorrência de algumas doenças crônicas não transmissíveis, com elevada prevalência na população atual. O microbioma intestinal pode ser um importante intermediário entre a saúde e bem estar do hospedeiro quando em equilíbrio, podendo vir a atuar como um coadjuvante no tratamento e prevenção de determinadas patologias, é notável que a prevalência de bactérias patogênicas gastrointestinais, causará um desgaste nas interações consideradas benéficas, levando o indivíduo ao estado patológico.