Efecto de IGF2 sobre el panorama de metilación del ADN y la expresión de ARNm asociada en la línea celular HTR-8/SVneo

ilustraciones, gráficas, tablas

Autores:
López González, David Alejandro
Tipo de recurso:
Fecha de publicación:
2021
Institución:
Universidad Nacional de Colombia
Repositorio:
Universidad Nacional de Colombia
Idioma:
spa
OAI Identifier:
oai:repositorio.unal.edu.co:unal/80620
Acceso en línea:
https://repositorio.unal.edu.co/handle/unal/80620
https://repositorio.unal.edu.co/
Palabra clave:
570 - Biología::572 - Bioquímica
Oncogenes
Metilación de ADN
Receptor IGF Tipo 2
Oncogenes
DNA Methylation
Receptor, IGF Type 2
Cáncer
Metilación del DNA
Placenta
Factor de crecimiento
Epigenética
Cancer
IGF signaling system
Epigenetics
Genomic instability
Genic expression
Malignant transformation
Rights
openAccess
License
Atribución-NoComercial-CompartirIgual 4.0 Internacional
id UNACIONAL2_1abc612225c87985c86faab72eecdeb0
oai_identifier_str oai:repositorio.unal.edu.co:unal/80620
network_acronym_str UNACIONAL2
network_name_str Universidad Nacional de Colombia
repository_id_str
dc.title.spa.fl_str_mv Efecto de IGF2 sobre el panorama de metilación del ADN y la expresión de ARNm asociada en la línea celular HTR-8/SVneo
dc.title.translated.eng.fl_str_mv Effect of IGF2 on the DNA methylation landscape and associated mRNA expression in HTR-8/SVneo cell line
title Efecto de IGF2 sobre el panorama de metilación del ADN y la expresión de ARNm asociada en la línea celular HTR-8/SVneo
spellingShingle Efecto de IGF2 sobre el panorama de metilación del ADN y la expresión de ARNm asociada en la línea celular HTR-8/SVneo
570 - Biología::572 - Bioquímica
Oncogenes
Metilación de ADN
Receptor IGF Tipo 2
Oncogenes
DNA Methylation
Receptor, IGF Type 2
Cáncer
Metilación del DNA
Placenta
Factor de crecimiento
Epigenética
Cancer
IGF signaling system
Epigenetics
Genomic instability
Genic expression
Malignant transformation
title_short Efecto de IGF2 sobre el panorama de metilación del ADN y la expresión de ARNm asociada en la línea celular HTR-8/SVneo
title_full Efecto de IGF2 sobre el panorama de metilación del ADN y la expresión de ARNm asociada en la línea celular HTR-8/SVneo
title_fullStr Efecto de IGF2 sobre el panorama de metilación del ADN y la expresión de ARNm asociada en la línea celular HTR-8/SVneo
title_full_unstemmed Efecto de IGF2 sobre el panorama de metilación del ADN y la expresión de ARNm asociada en la línea celular HTR-8/SVneo
title_sort Efecto de IGF2 sobre el panorama de metilación del ADN y la expresión de ARNm asociada en la línea celular HTR-8/SVneo
dc.creator.fl_str_mv López González, David Alejandro
dc.contributor.advisor.spa.fl_str_mv Umaña Pérez, Yadi Adriana
dc.contributor.author.spa.fl_str_mv López González, David Alejandro
dc.contributor.researchgroup.spa.fl_str_mv Grupo de Investigación en Hormonas
dc.subject.ddc.spa.fl_str_mv 570 - Biología::572 - Bioquímica
topic 570 - Biología::572 - Bioquímica
Oncogenes
Metilación de ADN
Receptor IGF Tipo 2
Oncogenes
DNA Methylation
Receptor, IGF Type 2
Cáncer
Metilación del DNA
Placenta
Factor de crecimiento
Epigenética
Cancer
IGF signaling system
Epigenetics
Genomic instability
Genic expression
Malignant transformation
dc.subject.decs.spa.fl_str_mv Oncogenes
Metilación de ADN
Receptor IGF Tipo 2
dc.subject.decs.eng.fl_str_mv Oncogenes
DNA Methylation
Receptor, IGF Type 2
dc.subject.proposal.spa.fl_str_mv Cáncer
Metilación del DNA
Placenta
Factor de crecimiento
Epigenética
dc.subject.proposal.eng.fl_str_mv Cancer
IGF signaling system
Epigenetics
Genomic instability
Genic expression
Malignant transformation
description ilustraciones, gráficas, tablas
publishDate 2021
dc.date.accessioned.none.fl_str_mv 2021-10-27T14:11:50Z
dc.date.available.none.fl_str_mv 2021-10-27T14:11:50Z
dc.date.issued.none.fl_str_mv 2021-07-28
dc.type.spa.fl_str_mv Trabajo de grado - Maestría
dc.type.driver.spa.fl_str_mv info:eu-repo/semantics/masterThesis
dc.type.version.spa.fl_str_mv info:eu-repo/semantics/acceptedVersion
dc.type.content.spa.fl_str_mv Text
dc.type.redcol.spa.fl_str_mv http://purl.org/redcol/resource_type/TM
status_str acceptedVersion
dc.identifier.uri.none.fl_str_mv https://repositorio.unal.edu.co/handle/unal/80620
dc.identifier.instname.spa.fl_str_mv Universidad Nacional de Colombia
dc.identifier.reponame.spa.fl_str_mv Repositorio Institucional Universidad Nacional de Colombia
dc.identifier.repourl.spa.fl_str_mv https://repositorio.unal.edu.co/
url https://repositorio.unal.edu.co/handle/unal/80620
https://repositorio.unal.edu.co/
identifier_str_mv Universidad Nacional de Colombia
Repositorio Institucional Universidad Nacional de Colombia
dc.language.iso.spa.fl_str_mv spa
language spa
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dc.format.extent.spa.fl_str_mv viii, 62 páginas
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dc.publisher.spa.fl_str_mv Universidad Nacional de Colombia
dc.publisher.program.spa.fl_str_mv Bogotá - Ciencias - Maestría en Ciencias - Bioquímica
dc.publisher.department.spa.fl_str_mv Departamento de Química
dc.publisher.faculty.spa.fl_str_mv Facultad de Ciencias
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dc.publisher.branch.spa.fl_str_mv Universidad Nacional de Colombia - Sede Bogotá
institution Universidad Nacional de Colombia
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spelling Atribución-NoComercial-CompartirIgual 4.0 Internacionalhttp://creativecommons.org/licenses/by-nc-sa/4.0/info:eu-repo/semantics/openAccesshttp://purl.org/coar/access_right/c_abf2Umaña Pérez, Yadi Adrianad652013090d46425f836051252c18e62López González, David Alejandro4fecb1c9885cec0383419bbf14e3e6d7Grupo de Investigación en Hormonas2021-10-27T14:11:50Z2021-10-27T14:11:50Z2021-07-28https://repositorio.unal.edu.co/handle/unal/80620Universidad Nacional de ColombiaRepositorio Institucional Universidad Nacional de Colombiahttps://repositorio.unal.edu.co/ilustraciones, gráficas, tablasEl proceso de implantación placentaria depende de una minuciosa regulación de la invasión de la decidua materna por parte del subtipo celular denominado trofoblasto extravelloso, la evasión del sistema inmune de la madre y la remodelación de la vasculatura local. Estos y otros procesos hacen que la implantación placentaria sea notablemente similar a la invasión tumoral. Las células de cáncer deben su origen a una pérdida de la identidad celular somática acompañada del desarrollo de un fenotipo aberrante que se alcanza como consecuencia de la reactivación de programas de desarrollo embrionario. Se cree que la pérdida de la identidad celular, así como la reactivación de los programas de desarrollo se deben en gran medida a una pérdida de la estabilidad genómica, que a su vez depende del panorama de metilación a nivel genómico. Se sabe que diversos estímulos extracelulares son capaces de promover una remodelación del panorama de metilación de células somáticas tal que contribuye a una transición maligna hacia un fenotipo altamente proliferativo e invasivo, que se debe tanto a la activación estocástica de oncogenes, como a un silenciamiento de genes supresores de tumores. Utilizando la línea celular derivada de trofoblasto, HTR-8/SVneo, por su fenotipo pseudomaligno y como modelo para el estudio de la biología placentaria y de la progresión tumoral, el propósito de este trabajo fue analizar la respuesta funcional de la línea ante un estímulo mitogénico con el péptido IGF2, y determinar cómo esta respuesta se relaciona con la variación en el panorama de metilación genómico y la expresión de RNA mensajero. A través de la interrogación del panorama de metilación genómico y la actividad transcripcional de la línea celular se identificaron variaciones que aparecen por efecto del estímulo y que ocurren de manera simultánea con un aumento de la actividad proliferativa, migratoria e invasiva de la línea celular. Muchos de los genes comprometidos en estas variaciones han sido descritos previamente en cáncer y más aún, hacen parte de vías de señalización a través de las cuales podría estar procediendo el estímulo con IGF2 y que además, son importantes para la adquisición de un fenotipo maligno en diversos tipos de cáncer. En conclusión, el péptido IGF2 tiene la capacidad de aumentar la actividad proliferativa, migratoria e invasiva de la línea celular, y estos cambios ocurren de manera paralela, y probablemente como consecuencia de alteraciones a nivel epigenético y transcripcional. (Texto tomado de la fuente)The process of placental implantation depends on a thorough regulation of the invasion of the maternal decidua by the cellular subtype known as extravillous trophoblast, invasion of the maternal immune system and remodeling of the local vasculature. These and other processes make the placental implantation remarkably similar to tumor invasion. Cancer cells owe their origin to a loss of somatic cellular identity, accompanied by the development of an aberrant phenotype achieved as a consequence of the stochastic reactivation of embryonic development programs. It is believed that this loss of cellular identity, as well as the reactivation of these programs is owed to a great extent to a loss of genomic stability, which in turn depends on the DNA methylation landscape at the genomic level. It has been observed that extracellular stimuli of diverse kinds are capable of promoting a remodeling of the DNA methylation landscape in somatic cell such that it contributes to a malignant transformation to a highly proliferative, migratory and invasive phenotype, which is owed both to a stochastic activation of oncogenes and a silencing of tumor-repressor genes. Using trophoblast-derived HTR-8/SVneo cell line because its pseudo malignant phenotype and as model for the study of placental biology and tumor progression, the purpose of this work was to analyze the functional response of the cell line as a response to a mitogenic stimulus with IGF2, and to determine how this response is related to the variation of the methylation landscape and the transcriptional activity of the cell line. Through interrogation of the genomic methylation landscape and the transcriptional activity of the cell line, some alterations were identified that appear as a consequence of the stimulus and that occur simultaneously with an increase of the proliferative, migratory and invasive activity of the cell line. Many of the genes compromised in these alterations have been previously described in cancer and moreover, take part in signaling pathways through which the IGF2 stimulus could be proceeding and that are important for the acquisition of a malignant phenotype in several types of cancer. In conclusion, IGF2 peptide has the capacity of promoting the proliferative, migratory and invasive capacities of the cell line and these changes happen simultaneously, and probably as a consequence of alterations at epigenetic and transcriptional levels.MaestríaMagíster en Ciencias - BioquímicaFactores de crecimiento, diferenciación y cáncerviii, 62 páginasapplication/pdfspaUniversidad Nacional de ColombiaBogotá - Ciencias - Maestría en Ciencias - BioquímicaDepartamento de QuímicaFacultad de CienciasBogotá, ColombiaUniversidad Nacional de Colombia - Sede Bogotá570 - Biología::572 - BioquímicaOncogenesMetilación de ADNReceptor IGF Tipo 2OncogenesDNA MethylationReceptor, IGF Type 2CáncerMetilación del DNAPlacentaFactor de crecimientoEpigenéticaCancerIGF signaling systemEpigeneticsGenomic instabilityGenic expressionMalignant transformationEfecto de IGF2 sobre el panorama de metilación del ADN y la expresión de ARNm asociada en la línea celular HTR-8/SVneoEffect of IGF2 on the DNA methylation landscape and associated mRNA expression in HTR-8/SVneo cell lineTrabajo de grado - Maestríainfo:eu-repo/semantics/masterThesisinfo:eu-repo/semantics/acceptedVersionTexthttp://purl.org/redcol/resource_type/TMBurrows, T. 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Nature. 417, 949–954Ministerio de Ciencia, Tecnología e InnovaciónInvestigadoresPúblico generalLICENSElicense.txtlicense.txttext/plain; charset=utf-83964https://repositorio.unal.edu.co/bitstream/unal/80620/1/license.txtcccfe52f796b7c63423298c2d3365fc6MD51ORIGINAL1013638215.2021.pdf1013638215.2021.pdfTesis de Maestría en Ciencias - Bioquímicaapplication/pdf1903587https://repositorio.unal.edu.co/bitstream/unal/80620/3/1013638215.2021.pdf16497d7e774c86057593af1a23adca53MD53THUMBNAIL1013638215.2021.pdf.jpg1013638215.2021.pdf.jpgGenerated Thumbnailimage/jpeg4860https://repositorio.unal.edu.co/bitstream/unal/80620/4/1013638215.2021.pdf.jpgf655ee719b7970a7287528d030c85b70MD54unal/80620oai:repositorio.unal.edu.co:unal/806202023-07-29 23:04:00.682Repositorio Institucional Universidad Nacional de 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GVyZWNob3MgZGUgYXV0b3IgcXVlIGNvbmxsZXZlIGxhIGRpc3RyaWJ1Y2nDs24gZGUgZXN0b3MgYXJjaGl2b3MgeSBtZXRhZGF0b3MuCkFsIGhhY2VyIGNsaWMgZW4gZWwgc2lndWllbnRlIGJvdMOzbiwgdXN0ZWQgaW5kaWNhIHF1ZSBlc3TDoSBkZSBhY3VlcmRvIGNvbiBlc3RvcyB0w6lybWlub3MuCgpVTklWRVJTSURBRCBOQUNJT05BTCBERSBDT0xPTUJJQSAtIMOabHRpbWEgbW9kaWZpY2FjacOzbiAyNy8yMC8yMDIwCg==