{"id":17282,"date":"2021-12-14T18:59:36","date_gmt":"2021-12-14T18:59:36","guid":{"rendered":"https:\/\/cancercentertec100.com\/?p=17282"},"modified":"2021-12-14T19:08:12","modified_gmt":"2021-12-14T19:08:12","slug":"noti-genetica-cancer-hereditario","status":"publish","type":"post","link":"https:\/\/cancercentertec100.com\/en\/noti-genetica\/noti-genetica-cancer-hereditario\/","title":{"rendered":"NOTI-GEN\u00c9TICA: ESTUDIOS GEN\u00c9TICOS III"},"content":{"rendered":"<p class=\"has-color-8-color has-text-color\">P<strong>or el Dr. Gildardo F. Zafra de la Rosa<\/strong><\/p>\n\n\n\n<p>Una de las razones por las que no se identifican mutaciones, en una familia con c\u00e1ncer hereditario, se debe a limitantes en las pruebas utilizadas, cuando no se usan todos los m\u00e9todos de laboratorio indicados, por ejemplo, solo una regi\u00f3n de los genes involucrados o solamente su secuenciaci\u00f3n y no MLPA. Muchos genes muestran deleciones o duplicaciones que no se detectan por el m\u00e9todo de secuenciaci\u00f3n, debido a que este m\u00e9todo analiza la secuencia de ambas cadenas de ADN o ARN y no detecta que a una le falta una regi\u00f3n porque compensa registrando a la cadena normal, graficando la secuencia como si estuviera completa.<\/p>\n\n\n\n<p>El M\u00e9todo de MLPA es de gran utilidad para demostrar alteraciones en el n\u00famero de copias de la secuencia del ADN. Este m\u00e9todo puede detectar hasta 50 secuencias gen\u00f3micas diferentes de ADN o de ARN.<\/p>\n\n\n\n<figure class=\"wp-block-image size-large\"><img loading=\"lazy\" decoding=\"async\" width=\"1024\" height=\"576\" src=\"https:\/\/cancercentertec100.com\/wp-content\/uploads\/2021\/12\/cancer_hereditario_2-1024x576.jpg\" alt=\"\" class=\"wp-image-17285\" srcset=\"https:\/\/cancercentertec100.com\/wp-content\/uploads\/2021\/12\/cancer_hereditario_2-1024x576.jpg 1024w, https:\/\/cancercentertec100.com\/wp-content\/uploads\/2021\/12\/cancer_hereditario_2-300x169.jpg 300w, https:\/\/cancercentertec100.com\/wp-content\/uploads\/2021\/12\/cancer_hereditario_2-768x432.jpg 768w, https:\/\/cancercentertec100.com\/wp-content\/uploads\/2021\/12\/cancer_hereditario_2-580x326.jpg 580w, https:\/\/cancercentertec100.com\/wp-content\/uploads\/2021\/12\/cancer_hereditario_2-860x484.jpg 860w, https:\/\/cancercentertec100.com\/wp-content\/uploads\/2021\/12\/cancer_hereditario_2-1160x653.jpg 1160w, https:\/\/cancercentertec100.com\/wp-content\/uploads\/2021\/12\/cancer_hereditario_2.jpg 1200w\" sizes=\"auto, (max-width: 1024px) 100vw, 1024px\" \/><\/figure>\n\n\n\n<p>El m\u00e9todo de MLPA es una amplificaci\u00f3n m\u00faltiple de material gen\u00e9tico dependiente del ligamiento de sondas, consiste en amplificar diferentes fragmentos de ADN (sondas ligadas) en una misma reacci\u00f3n. Con ello es posible determinar la dosis g\u00e9nica en pacientes con grandes deleciones o amplificaciones y delimitar la extensi\u00f3n del rearreglo y los puntos de ruptura de la cadena de ADN. En la reacci\u00f3n, cada secuencia del ADN blanco es reconocida por una sonda conformada por dos mitades, si la secuencia tiene complementariedad, ambas sondas se encontrar\u00e1n, interpret\u00e1ndose como \u00edntegra, en cambio si falta un segmento de material gen\u00e9tico, las sondas no se encontrar\u00e1n y se interpretar\u00e1 como un deleci\u00f3n; o una amplificaci\u00f3n en caso que las sondas se encuentren en trayectos m\u00e1s largos.<\/p>\n\n\n\n<p>En el caso del c\u00e1ncer de mama, por ejemplo, se emplea el m\u00e9todo de MLPA debido a que en ciertas poblaciones hasta un 20% puede deberse a deleciones.<\/p>","protected":false},"excerpt":{"rendered":"<p>Por el Dr. Gildardo F. Zafra de la Rosa Una de las razones por las que no se identifican mutaciones, en una familia con c\u00e1ncer hereditario, se debe a limitantes en las pruebas utilizadas, cuando no se usan todos los m\u00e9todos de laboratorio indicados, por ejemplo, solo una regi\u00f3n de los genes involucrados o solamente&#8230;<\/p>","protected":false},"author":1,"featured_media":17286,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[293],"tags":[26,36,295,294],"class_list":["post-17282","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-noti-genetica","tag-cancer","tag-cancer-center-tec-100","tag-hereditario","tag-notigenetica"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.4 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>NOTI-GEN\u00c9TICA: ESTUDIOS GEN\u00c9TICOS III<\/title>\n<meta name=\"description\" content=\"Por el Dr. Gildardo F. 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