Publications by authors named "Daniele Sa Pereira"

The relationship between the (rs16944) polymorphism and the risk of developing hematologic malignancies remains controversial. Thus, we performed a meta-analysis to evaluate the association between polymorphism and the risk of developing hematologic malignancies. A comprehensive search was conducted to identify all eligible studies on polymorphism and hematologic malignancies.

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Acute lymphoblastic leukemia (ALL) is the most common pediatric cancer in the world, and accounts for 25% of all childhood cancers among children under 15 years of age. Longitudinal studies have shown that children with ALL are born with a deregulated immune response that, together with postnatal environmental exposures, favor the onset of the disease. In this context, IL-10, a key cytokine in the regulation of the immune response, presents itself as a paradoxical mediator, initially influencing the development of ALL through the regulation of inflammatory processes and later on the progression of malignancy, with the increase of this molecule in the leukemia microenvironment.

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Inflammation is a physiological mechanism of the immune response and has an important role in maintaining the hematopoietic cell niche in the bone marrow. During this process, the participation of molecules produced by innate immunity cells in response to a variety of pathogen-associated molecular patterns and damage-associated molecular patterns is observed. However, chronic inflammation is intrinsically associated with leukemogenesis, as it induces DNA damage in hematopoietic stem cells and contributes to the creation of the preleukemic clone.

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Acute lymphoblastic leukemia (ALL) is the most common hematologic malignancy in children in childhood. Single-nucleotide polymorphism (SNPs) in key molecules of the immune system, such as Toll-like receptors (TLRs) and CD14 molecules, are associated with the development of several diseases. However, their role in ALL is unknown.

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Article Synopsis
  • - A study investigated the link between inflammasome genes and childhood leukemia by comparing 158 patients with acute lymphoblastic leukemia (ALL) to 192 healthy controls.
  • - Genetic analysis revealed that the IL1B C/T rs19644 variant increased the risk of developing ALL, while the NLRP1 A/T rs12150220 variant appeared to provide some protection against infections.
  • - No significant associations were found for NLRP3 and P2RX7 variants, indicating that more research with larger groups is needed to confirm the role of these genetic variants in childhood leukemia.
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