학술논문
Mucin (MUC) Family Influence on Acute Lymphoblastic Leukemia in Cancer and Non-Cancer Native American Populations from the Brazilian Amazon.
Document Type
Article
Author
Alcântara, Angélica Leite de; Pastana, Lucas Favacho; Gellen, Laura Patrícia Albarello; Vieira, Giovana Miranda; Dobbin, Elizabeth Ayres Fragoso; Silva, Thays Amâncio; Pereira, Esdras Edgar Batista; Rodrigues, Juliana Carla Gomes; Guerreiro, João Farias; Fernandes, Marianne Rodrigues; Assumpção, Paulo Pimentel de; Cohen-Paes, Amanda de Nazaré; Santos, Sidney Emanuel Batista Dos; Santos, Ney Pereira Carneiro dos
Source
Subject
*INDIGENOUS peoples of South America
*NATIVE Americans
*LYMPHOBLASTIC leukemia
*ACUTE leukemia
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Language
ISSN
2075-4426
Abstract
The mucin (MUC) family includes several genes aberrantly expressed in multiple carcinomas and mediates diverse pathways essentials for oncogenesis, in both solid and hematological malignancies. Acute Lymphoblastic Leukemia (ALL) can have its course influenced by genetic variants, and it seems more frequent in the Amerindian population, which has been understudied. Therefore, the present work aimed to investigate the MUC family exome in Amerindian individuals from the Brazilian Amazon, in a sample containing healthy Native Americans (NAMs) and indigenous subjects with ALL, comparing the frequency of polymorphisms between these two groups. The population was composed of 64 Amerindians from the Brazilian Amazon, from 12 different isolated tribes, five of whom were diagnosed with ALL. We analyzed 16 genes from the MUC family and found a total of 1858 variants. We compared the frequency of each variant in the ALL vs. NAM group, which led to 77 variants with a significant difference and, among these, we excluded those with a low impact, resulting in 63 variants, which were distributed in nine genes, concentrated especially in MUC 19 (n = 30) and MUC 3A (n = 18). Finally, 11 new variants were found in the NAM population. This is the first work with a sample of native Americans with cancer, a population which is susceptible to ALL, but remains understudied. The MUC family seems to have an influence on the development of ALL in the Amerindian population and especially MUC19 and MUC3A are shown as possible hotspots. In addition, the 11 new variants found point to the need to have their clinical impact analyzed. [ABSTRACT FROM AUTHOR]