Publications by authors named "Darlen Cardoso Carvalho"

Genetic variations in have been associated with different pathologies in global literature, but there are no data regarding this gene in Native American populations. The Amazonian Native American populations have lower genetic diversity and are more different from other continental groups. We investigated 18 genetic variants in the gene in Amazonian indigenous and compared our results with the ones found in global populations, which were publicly available in the 1000 Genomes Project, gnmAD and ABraOM databases.

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  • Acute Lymphoblastic Leukemia (ALL) is the most common cancer in children, and this study looks into genetic variations affecting the microRNAs related to its development in a Brazilian population.
  • The study analyzed 10 genetic polymorphisms in 100 pediatric ALL patients and 180 healthy controls, finding that specific genotypes significantly increased the risk of developing ALL, particularly the rs3746444 and rs3805500 polymorphisms.
  • Results indicate that certain genetic variations can indicate susceptibility to ALL, highlighting their potential use in risk assessment and facilitating a better understanding of the disease's complex causes.
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Colorectal (CRC) and gastric (GC) cancers are associated with increased morbidity and mortality. Single nucleotide polymorphisms (SNPs) of xenobiotic metabolism and transporter genes may play a role in the individual responses to exposure to substances implicated in susceptibility to cancer. The investigation of the genetic variation related to the activation and detoxification of xenobiotics may thus help to clarify the prevalence of neoplasms.

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  • - Acute Lymphoblastic Leukemia (ALL) is the most common childhood cancer, but treatment outcomes vary among different ethnic groups, particularly showing lower success rates in children with high Native American ancestry.
  • - A study analyzed 27 genetic markers related to ALL treatment in Amerindian populations from the Brazilian Amazon and compared these to data from five continents, revealing significant differences in marker frequencies.
  • - The unique genetic profile of the indigenous Amazonian population suggests they may require tailored treatment strategies for ALL due to their distinct pharmacogenomic variants.
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Acute Lymphoblastic Leukemia (ALL) is the most common childhood neoplasia. Studies have shown that susceptibility to ALL may be modulated by genetic variables. Our study investigated 21 genetic variants in the susceptibility of the population of the Brazilian Amazon region to B-cell ALL.

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The treatment of Acute Lymphoblastic Leukemia (ALL) in children has a high clinical success rate, although toxicological complications are frequent, and often result in the interruption of the treatment. Various studies have shown that toxicities resulting from the treatment are influenced by pharmacogenetic variants. Most of this research has focused on relatively homogeneous populations, and the influence of these variants in highly admixed populations, such as that of Brazil, is still poorly understood.

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Following publication of the original article [1], the authors requested a correction to the name of one of the co-authors. The correct name Marianne Rodrigues Fernandes, not Marianne Fernandes Rodrigues.

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Background: Global literature describes differences in the incidence of gastric cancer among populations. For instance, Europeans have lower incidence rates of gastric cancer in relation to Latin and Asian populations, particularly Korean and Japanese populations. However, only a few studies have been able to verify the occurrence of gastric cancer in admixed populations with high interethnic degree mix, such as the Brazilian Amazon region.

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  • * Methods: Researchers analyzed genetic data from 1,038 people, including a specific group of 127 individuals from Brazil, looking at allele distribution and similarities to other populations.
  • * Results: The findings revealed that 37% of the population carried at least three harmful genetic variations, and 38.6% had one harmful variation in homozygous form, suggesting the need for genetic testing before treatment.
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Background: The N-acetyltransferase 2 (NAT2) gene is a marker for the study of interindividual susceptibility to developing neoplasias. The purpose of this study was to verify a possible association between single nucleotide polymomorphisms (SNPs) of NAT2 and the susceptibility to gastric cancer (GC) and breast cancer (BC) in patients from the North region of Brazil.

Materials And Methods: Five SNPs of the NAT2 gene were investigated by direct sequencing.

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