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Campo DCValorLengua/Idioma
dc.creatorPartida Pérez, Miriam-
dc.creatorAyala Madrigal, María  de la Luz-
dc.creatorPeregrina Sandoval, Jorge-
dc.creatorMacías Gómez, Nelly-
dc.creatorMoreno Ortiz, José-
dc.creator Leal Ugarte, Evelia-
dc.creatorCárdenas Meza, Mario-
dc.creatorCenteno Flores, Manuel-
dc.creatorMaciel Gutiérrez, Víctor-
dc.creatorCabrales, Enrique-
dc.creatorCervantes Ortiz, Sergio-
dc.creatorGutiérrez Angulo, Melva-
dc.date2015-08-17T14:34:45Z-
dc.date2015-08-17T14:34:45Z-
dc.date2010-
dc.date.accessioned2019-04-07T23:48:11Z-
dc.date.available2019-04-07T23:48:11Z-
dc.identifier1574-0153 (P)-
dc.identifier1875-8592 (E)-
dc.identifierDOI: 10.3233/CBM-2010-0154-
dc.identifierhttp://repositorio.cualtos.udg.mx:8080/jspui/handle/123456789/376-
dc.identifier.urihttps://hdl.handle.net/20.500.12104/72568-
dc.descriptionLeptin and adiponectin are cytokines produced by adipose tissue with opposite effects on tumor growth: the former stimulate whereas the latter inhibit it. The objective was to analyze the association of LEP A19G and ADIPOQ+45 T/G and +276 G/T polymorphisms in Mexican patients with colorectal cancer (CRC). 68 unrelated patients with CRC (study group) and 102 blood donors (control group); all subjects were Mestizos from western Mexico. The polymorphisms were established by PCR-RFLP on DNA samples obtained from peripheral blood. The LEP A19G polymorphism showed significant differences between CRC patients and control group (p= 0.01 for G/A genotype and p= 0.02 for the recessive model G/G +G/A); yet, in the analysis stratified by gender, this difference remained significant only in males. The ADIPOQ polymorphisms did not shown any significant differences. Our results suggest that the A19G LEP polymorphism is associated with CRC in Mexican patients.-
dc.descriptionInstituto de Genética Humana, CUCS, Universidad de Guadalajara.-
dc.languageen-
dc.relationCancer Biomarkers;vol. 7, no. 3, 2010, pp. 117-121-
dc.titleAssociation of LEP and ADIPOQ common variants with colorectal cancer in Mexican patients.-
dc.typeArticle-
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