Natural and synthetic retinoids in preclinical colorectal cancer models

dc.contributor.authorAbdel-Samad, Rana
dc.contributor.authorAouad, Patrick
dc.contributor.authorDarwiche, Nadine D.
dc.contributor.departmentBiochemistry and Molecular Genetics
dc.contributor.facultyFaculty of Medicine (FM)
dc.contributor.institutionAmerican University of Beirut
dc.date.accessioned2025-01-24T11:37:59Z
dc.date.available2025-01-24T11:37:59Z
dc.date.issued2019
dc.description.abstractColorectal cancer (CRC) remains a leading cause of cancer-related morbidity and mortality worldwide. Although targeted therapy in combination with chemotherapy in CRC prolongs the overall survival of patients with metastatic disease, acquired resistance and relapse hinder their clinical benefits. Moreover, patients with some specific genetic profile are unlikely to benefit from targeted therapy, suggesting the need for safe and effective treatment strategies. Retinoids, comprising of natural and synthetic analogs, are a class of chemical compounds that regulate cellular proliferation, differentiation, and cell death. Retinoids have been used in the clinic for several leukemias and solid tumors, either as single agents or in combination therapy. Furthermore, retinoids have shown potent chemotherapeutic and chemopreventive properties in different cancer models, including CRC. In this review, we summarize the major preclinical findings in CRC in which natural and synthetic retinoids showed promising antitumor activities and stress on the proposed mechanisms of action. Understanding of the retinoids' antitumor mechanisms would provide insights to support and warrant their development in the management of CRC. © 2019 Lippincott Williams and Wilkins. All rights reserved.
dc.identifier.doihttps://doi.org/10.1097/CAD.0000000000000802
dc.identifier.eid2-s2.0-85069889442
dc.identifier.pmid31021825
dc.identifier.urihttp://hdl.handle.net/10938/28948
dc.language.isoen
dc.publisherLippincott Williams and Wilkins
dc.relation.ispartofAnti-Cancer Drugs
dc.sourceScopus
dc.subjectColorectal cancer
dc.subjectNatural retinoids
dc.subjectPreclinical models
dc.subjectRetinoic acid
dc.subjectSynthetic retinoids
dc.subjectAnimals
dc.subjectBiological products
dc.subjectCell proliferation
dc.subjectColorectal neoplasms
dc.subjectDrug evaluation, preclinical
dc.subjectHumans
dc.subjectRetinoids
dc.subject2 (carboxyphenyl)retinamide
dc.subject6 oh 11 o hydroxyphenanthrene
dc.subject6 [3 (1 adamantyl) 4 hydroxyphenyl] 2 naphthoic acid
dc.subjectAdarotene
dc.subjectBexarotene
dc.subjectButenolide
dc.subjectMofarotene
dc.subjectPeretinoin
dc.subjectPhenanthrene derivative
dc.subjectRetinoid
dc.subjectRetinoid x receptor
dc.subjectRetinoidal
dc.subjectUnclassified drug
dc.subjectBiological product
dc.subjectAntineoplastic activity
dc.subjectDrug efficacy
dc.subjectDrug mechanism
dc.subjectNonhuman
dc.subjectPreclinical study
dc.subjectPriority journal
dc.subjectReview
dc.subjectAnimal
dc.subjectColorectal tumor
dc.subjectHuman
dc.subjectPathology
dc.titleNatural and synthetic retinoids in preclinical colorectal cancer models
dc.typeReview

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