Polimorfismos genéticos de interleucinas IL-1B-511, IL-1RN, IL-10, factor de necrosis tumoral α-308 e infección por Helicobacter pylori CagA positivo en cáncer gástrico y úlcera duodenal en diferentes poblaciones en Colombia

Autores/as

  • Teresa Martínez Instituto Nacional de Cancerología
  • Gustavo Hernández Instituto Nacional de Cancerología
  • María M. Bravo Instituto Nacional de Cancerología
  • Esperanza Trujillo Instituto Nacional de Cancerología
  • Andrés Quiroga Instituto Nacional de Cancerología
  • Juan C. Robayo Fundación Santa Fe
  • Jesús Pérez Clínica General del Norte
  • Juan C. Bravo Fundación Valle del Lili
  • Margarita Camorlinga Instituto Mexicano de Seguros Sociales

Palabras clave:

Interleucinas 1B, 10, factor de necrosis tumoral alpha, Helicobacter pylori, proteína cagA, neoplasias de estomago, ulcera duodenal

Resumen

Objetivo: Determinar la asociación entre los polimorfismos IL-1B-511, IL-1RN, TNF-α-308, IL-10-819 e IL-101082 y la infección por Helicobacter pylori CagA positivo en un grupo de pacientes con cáncer gástrico y úlcera duodenal en diferentes poblaciones en Colombia.
Métodos: Estudio de casos y controles con 341 pacientes: con gastritis no atrófica, 194; con cáncer gástrico, 58; úlcera duodenal con lesiones preneoplásicas, 54; y con úlcera duodenal, 35. La genotipificación de los polimorfismos se hizo por discriminación alélica usando PCR en tiempo real, y la del IL-1RN, por PCR convencional y electroforesis en agarosa. La infección por Helicobacter pylori CagA se determinó mediante ELISA. Se utilizó la regresión logística en el análisis estadístico.
Resultados: Ser portador del genotipo IL-1B-511TT (OR=4,69; IC 95% 1,22-18,09) y tener una infección por Helicobacter pylori CagA positivo (OR=4,43; IC 95% 1,72-11,4) se asociaron a cáncer gástrico. Tener una infección por Helicobacter pylori CagA positivo (OR=4,39; IC95% 1,82-10,59) se asoció a la presencia de úlcera duodenal con lesiones preneoplásicas, y ser portador del genotipo IL-1B-511CT se asoció a úlcera duodenal (OR=0,30; IC 95% 0,10-0,91).
Conclusión: Los resultados sugieren que la respuesta pro-inflamatoria y la genética virulenta de la bacteria son factores relacionados con los diferentes desenlaces ocasionados por la infección por Helicobacter pylori en la población estudiada; así, el polimorfismo IL-1B-511 es un factor relacionado con cáncer gástrico y úlcera duodenal, y la infección por Helicobacter pylori CagA positivo es un factor asociado a cáncer gástrico y úlcera duodenal con lesiones preneoplásicas.

Biografía del autor/a

Teresa Martínez, Instituto Nacional de Cancerología

Grupo de Investigación Epidemiológica del Cáncer, Instituto Nacional de Cancerología, Bogotá D.C., Colombia

Gustavo Hernández, Instituto Nacional de Cancerología

Grupo de Investigación Epidemiológica del Cáncer, Instituto Nacional de Cancerología, Bogotá D.C., Colombia

María M. Bravo, Instituto Nacional de Cancerología

Grupo de Biología del Cáncer, Instituto Nacional de Cancerología, Bogotá D.C., Colombia

Esperanza Trujillo, Instituto Nacional de Cancerología

Grupo de Biología del Cáncer, Instituto Nacional de Cancerología, Bogotá D.C., Colombia

Andrés Quiroga, Instituto Nacional de Cancerología

Grupo de Biología del Cáncer, Instituto Nacional de Cancerología, Bogotá D.C., Colombia

Juan C. Robayo, Fundación Santa Fe

Departamento de Gastroenterología, Fundación Santa Fe, Bogotá D. C., Colombia

Jesús Pérez, Clínica General del Norte

Grupo de investigación, Clínica General del Norte, Barranquilla, Colombia

Juan C. Bravo, Fundación Valle del Lili

Departamento de Patología, Fundación Valle del Lili, Cali, Valle, Colombia

Margarita Camorlinga, Instituto Mexicano de Seguros Sociales

Hospital de Pediatría CMN Siglo XXI, Instituto Mexicano de Seguros Sociales, Ciudad de México, México

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Cómo citar

[1]
Martínez, T. et al. 2011. Polimorfismos genéticos de interleucinas IL-1B-511, IL-1RN, IL-10, factor de necrosis tumoral α-308 e infección por Helicobacter pylori CagA positivo en cáncer gástrico y úlcera duodenal en diferentes poblaciones en Colombia. Revista Colombiana de Cancerología. 15, 2 (jun. 2011), 85–97.

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