Association between genetic variant rs2267716 of

Alleles Case-Control Studies Colorectal Neoplasms / genetics Corticotropin-Releasing Hormone / genetics Cross-Sectional Studies Genetic Predisposition to Disease Humans Polymorphism, Single Nucleotide / genetics Receptors, Corticotropin-Releasing Hormone / genetics
carcinogenesis colorectal neoplasms genetic polymorphism restriction fragment length

Journal

Journal of investigative medicine : the official publication of the American Federation for Clinical Research
ISSN: 1708-8267
Titre abrégé: J Investig Med
Pays: England
ID NLM: 9501229

Informations de publication

Date de publication:
04 2022
Historique:
accepted: 24 11 2021
pubmed: 1 1 2022
medline: 14 4 2022
entrez: 31 12 2021
Statut: ppublish

Résumé

Colorectal cancer (CRC) is the third most common cancer and one of the main causes of death around the world. Multiple lines of evidence have suggested the role of the corticotropin-releasing hormone (CRH) family in CRC induction, including the low expression of corticotropin-releasing hormone receptor 2 (

Identifiants

DOI: 10.1136/jim-2021-002047 PMID: 34969780
pubmed: 34969780
pii: jim-2021-002047
doi: 10.1136/jim-2021-002047
doi:

Substances chimiques

CRF receptor type 2 0
Receptors, Corticotropin-Releasing Hormone 0
Corticotropin-Releasing Hormone 9015-71-8

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

947-952

Informations de copyright

© American Federation for Medical Research 2022. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: None declared.

Auteurs

Angélica Araceli Ramírez-Guerrero (AA)

Facultad de Medicina, Universidad de Colima, Colima, Mexico.

Christian Octavio González-Villaseñor (CO)

Laboratorio de Genética Humana, Universidad de Guadalajara Campus Centro Universitario del Sur, Ciudad Guzmán, Mexico.

Evelia Leal-Ugarte (E)

Facultad de Medicina, Universidad Autónoma de Tamaulipas Facultad de Ingeniería y Ciencias, Matamoros, Tamaulipas, Mexico.

Melva Gutiérrez-Angulo (M)

Ciencias de la Salud, Universidad de Guadalajara-Centro Universitario Los Altos, Tepatitlan de Morelos, Mexico.

Mario Ramírez-Flores (M)

Facultad de Medicina, Universidad de Colima, Colima, Mexico.

Iván Delgado-Enciso (I)

Facultad de Medicina, Universidad de Colima, Colima, Mexico.

Nelly Margarita Macías-Gómez (NM)

Laboratorio de Genética Humana, Universidad de Guadalajara Campus Centro Universitario del Sur, Ciudad Guzmán, Mexico nellymacias_2000@yahoo.com.mx.
ORCID: 0000-0002-0878-2401

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Classifications MeSH

questionsmedicales.fr › Phénomènes génétiques › Structures génétiques › Génome › Composants de génome › Gènes › Allèles › Association between genetic variant rs2267716 of
questionsmedicales.fr › Environnement et santé publique › Santé publique › Méthodes épidémiologiques › Caractéristiques des études épidémiologiques › Études épidémiologiques › Études cas-témoins › Association between genetic variant rs2267716 of
questionsmedicales.fr › Maladies de l'appareil digestif › Maladies gastro-intestinales › Maladies intestinales › Maladies du rectum › Tumeurs colorectales › Association between genetic variant rs2267716 of
questionsmedicales.fr › Acides aminés, peptides et protéines › Protéines › Protéines de tissu nerveux › Neuropeptides › Hormones hypothalamiques › Hormones hypophysiotropes libératrices › Corticolibérine › Association between genetic variant rs2267716 of
questionsmedicales.fr › Environnement et santé publique › Santé publique › Méthodes épidémiologiques › Caractéristiques des études épidémiologiques › Études épidémiologiques › Études transversales › Association between genetic variant rs2267716 of
questionsmedicales.fr › Phénomènes génétiques › Génotype › Prédisposition génétique à une maladie › Association between genetic variant rs2267716 of
questionsmedicales.fr › Eucaryotes › Animaux › Chordés › Vertébrés › Mammifères › Eutheria › Primates › Haplorhini › Catarrhini › Hominidae › Humains › Association between genetic variant rs2267716 of
questionsmedicales.fr › Phénomènes génétiques › Variation génétique › Polymorphisme génétique › Polymorphisme de nucléotide simple › Association between genetic variant rs2267716 of
questionsmedicales.fr › Acides aminés, peptides et protéines › Protéines › Protéines membranaires › Récepteurs de surface cellulaire › Récepteurs peptidiques › Récepteur hormones hypothalamiques hypophysotropes régulatrices › Récepteur CRH › Association between genetic variant rs2267716 of