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  1. Article ; Online: ARID5B, CEBPE and PIP4K2A Germline Genetic Polymorphisms and Risk of Childhood Acute Lymphoblastic Leukemia in Mexican Patients: A MIGICCL Study.

    Bekker-Méndez, Vilma Carolina / Núñez-Enríquez, Juan Carlos / Torres Escalante, José Luis / Alvarez-Olmos, Enrique / González-Montalvoc, Pablo Miguel / Jiménez-Hernández, Elva / Sansón, Aurora Medina / Leal, Yelda A / Ramos-Cervantes, María Teresa / Guerra-Castillo, Francisco Xavier / Ortiz-Maganda, Mónica Patricia / Flores-Lujano, Janet / Pérez-Saldivar, Maria Luisa / Velazquez-Aviña, Martha Margarita / Bolea-Murga, Victoria / Torres-Nava, José Refugio / Amador-Sanchez, Raquel / Solis-Labastida, Karina Anastacia / Rámirez-Bello, Julian /
    Fragoso, José Manuel / Mejía-Aranguré, Juan Manuel

    Archives of medical research

    2017  Volume 47, Issue 8, Page(s) 623–628

    Abstract: Background and aims: Childhood acute lymphoblastic leukemia (ALL) is the leading cause of childhood cancer-related deaths worldwide. Multiples studies have shown that ALL seems to be originated by an interaction between environmental and genetic ... ...

    Abstract Background and aims: Childhood acute lymphoblastic leukemia (ALL) is the leading cause of childhood cancer-related deaths worldwide. Multiples studies have shown that ALL seems to be originated by an interaction between environmental and genetic susceptibility factors. The ARID5B polymorphisms are among the most reproducible ALL associated-risk alleles in different populations. The aim of the present study was to examine the contribution of ARID5B, CEBPE, and PIP4K2 risk alleles for the development of ALL in children from Mexico City and Yucatan, Mexico.
    Methods: A study was conducted with a total of 761 unrelated subjects. Two hundred eighty five ALL cases (111 from Yucatan and 174 from Mexico City) and 476 healthy subjects. Genotyping included the rs7088318 (PIP4K2A), rs10821936 (ARID5B), rs7089424 (ARID5B) and rs2239633 (CEBPE) polymorphisms.
    Results: Associations between ALL and rs10821936 and rs7089424 ARID5B SNPs were found (OR = 1.9, 95% CI (1.5-2.4) and OR = 2.0, 95% CI (1.6-2.5), respectively). Moreover, a higher risk was observed in the homozygous risk genotypes of carriers from Mexico City (OR = 3.1, 95% CI (2.0-4.9) and OR 3.1, CI 95% (2.0-4.8), respectively). Otherwise, the rs7088318 (PIP4K2A) and rs2239633 (CEBPE) polymorphisms were not associated with ALL risk.
    Conclusions: Our analysis suggests that ARID5B confers risk for childhood ALL in a Mexican population.
    MeSH term(s) Adolescent ; Alleles ; CCAAT-Enhancer-Binding Proteins/genetics ; Case-Control Studies ; Child ; Child, Preschool ; DNA-Binding Proteins/genetics ; Female ; Genetic Association Studies ; Genetic Predisposition to Disease ; Genotype ; Heterozygote ; Humans ; Infant ; Male ; Mexico ; Phosphotransferases (Alcohol Group Acceptor)/genetics ; Polymorphism, Single Nucleotide ; Precursor Cell Lymphoblastic Leukemia-Lymphoma/genetics ; Risk ; Transcription Factors/genetics
    Chemical Substances ARID5B protein, human ; CCAAT-Enhancer-Binding Proteins ; DNA-Binding Proteins ; Transcription Factors ; CEBPE protein, human (142805-41-2) ; PIP4K2A protein, human (EC 2.7.1.-) ; Phosphotransferases (Alcohol Group Acceptor) (EC 2.7.1.-)
    Language English
    Publishing date 2017-05-04
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 1156844-6
    ISSN 1873-5487 ; 0188-4409 ; 0188-0128
    ISSN (online) 1873-5487
    ISSN 0188-4409 ; 0188-0128
    DOI 10.1016/j.arcmed.2016.12.003
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Identification and Characterization of Novel Fusion Genes with Potential Clinical Applications in Mexican Children with Acute Lymphoblastic Leukemia.

    Mata-Rocha, Minerva / Rangel-López, Angelica / Jiménez-Hernández, Elva / Morales-Castillo, Blanca Angélica / González-Torres, Carolina / Gaytan-Cervantes, Javier / Álvarez-Olmos, Enrique / Núñez-Enríquez, Juan Carlos / Fajardo-Gutiérrez, Arturo / Martín-Trejo, Jorge Alfonso / Solís-Labastida, Karina Anastacia / Medina-Sansón, Aurora / Flores-Lujano, Janet / Sepúlveda-Robles, Omar Alejandro / Peñaloza-González, José Gabriel / Espinoza-Hernández, Laura Eugenia / Núñez-Villegas, Nora Nancy / Espinosa-Elizondo, Rosa Martha / Cortés-Herrera, Beatriz /
    Torres-Nava, José Refugio / Flores-Villegas, Luz Victoria / Merino-Pasaye, Laura Elizabeth / Bekker-Méndez, Vilma Carolina / Velázquez-Aviña, Martha Margarita / Pérez-Saldívar, María Luisa / Bautista-Martínez, Benito Alejandro / Amador-Sánchez, Raquel / González-Avila, Ana Itamar / Jiménez-Morales, Silvia / Duarte-Rodríguez, David Aldebarán / Santillán-Juárez, Jessica Denisse / García-Velázquez, Alejandra Jimena / Rosas-Vargas, Haydeé / Mejía-Aranguré, Juan Manuel

    International journal of molecular sciences

    2019  Volume 20, Issue 10

    Abstract: Acute lymphoblastic leukemia is the most common type of childhood cancer worldwide. Mexico City has one of the highest incidences and mortality rates of this cancer. It has previously been recognized that chromosomal translocations are important in ... ...

    Abstract Acute lymphoblastic leukemia is the most common type of childhood cancer worldwide. Mexico City has one of the highest incidences and mortality rates of this cancer. It has previously been recognized that chromosomal translocations are important in cancer etiology. Specific fusion genes have been considered as important treatment targets in childhood acute lymphoblastic leukemia (ALL). The present research aimed at the identification and characterization of novel fusion genes with potential clinical implications in Mexican children with acute lymphoblastic leukemia. The RNA-sequencing approach was used. Four fusion genes not previously reported were identified:
    MeSH term(s) Adolescent ; Adult ; CREB-Binding Protein/genetics ; Child ; Child, Preschool ; Dyneins/genetics ; Female ; GTPase-Activating Proteins/genetics ; Gene Expression Regulation, Neoplastic ; Gene Rearrangement ; Humans ; Ikaros Transcription Factor/genetics ; Infant ; Male ; Mexico ; Nuclear Proteins/genetics ; Oncogene Proteins, Fusion/genetics ; Precursor Cell Lymphoblastic Leukemia-Lymphoma/genetics ; Prognosis ; Proto-Oncogene Proteins c-ets/genetics ; RNA Cap-Binding Proteins/genetics ; RNA-Binding Proteins/genetics ; Receptors, Cytoplasmic and Nuclear/genetics ; Repressor Proteins/genetics ; Translocation, Genetic/genetics ; Young Adult ; ETS Translocation Variant 6 Protein
    Chemical Substances GTPase-Activating Proteins ; IKZF1 protein, human ; NUFIP1 protein, human ; Nuclear Proteins ; Oncogene Proteins, Fusion ; Proto-Oncogene Proteins c-ets ; RNA Cap-Binding Proteins ; RNA-Binding Proteins ; Receptors, Cytoplasmic and Nuclear ; Repressor Proteins ; SNUPN protein, human ; SRGAP3 protein, human ; Ikaros Transcription Factor (148971-36-2) ; CREB-Binding Protein (EC 2.3.1.48) ; CREBBP protein, human (EC 2.3.1.48) ; DNAH14 protein, human (EC 3.6.4.2) ; Dyneins (EC 3.6.4.2)
    Language English
    Publishing date 2019-05-15
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2019364-6
    ISSN 1422-0067 ; 1422-0067 ; 1661-6596
    ISSN (online) 1422-0067
    ISSN 1422-0067 ; 1661-6596
    DOI 10.3390/ijms20102394
    Database MEDical Literature Analysis and Retrieval System OnLINE

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