Indole-3-Carbinol, a Phytochemical Aryl Hydrocarbon Receptor-Ligand, Induces the mRNA Overexpression of UBE2L3 and Cell Proliferation Arrest

Cervical cancer (CC) is one of the most common cancers in women, and is linked to human papillomavirus (HPV) infection. The virus oncoprotein E6 binds to p53, resulting in its degradation and allowing uncontrolled cell proliferation. Meanwhile, the HPV E7 protein maintains host cell differentiation...

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Veröffentlicht in:Current issues in molecular biology 2022-05, Vol.44 (5), p.2054-2068
Hauptverfasser: Arellano-Gutiérrez, Claudia Vanessa, Quintas-Granados, Laura Itzel, Cortés, Hernán, González Del Carmen, Manuel, Leyva-Gómez, Gerardo, Bustamante-Montes, Lilia Patricia, Rodríguez-Morales, Miguel, López-Reyes, Israel, Padilla-Mendoza, Juan Ramón, Rodríguez-Páez, Lorena, Figueroa-González, Gabriela, Reyes-Hernández, Octavio Daniel
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Sprache:eng
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Zusammenfassung:Cervical cancer (CC) is one of the most common cancers in women, and is linked to human papillomavirus (HPV) infection. The virus oncoprotein E6 binds to p53, resulting in its degradation and allowing uncontrolled cell proliferation. Meanwhile, the HPV E7 protein maintains host cell differentiation by targeting retinoblastoma tumor suppressor. The host cell can ubiquitinate E6 and E7 through UBE2L3, whose expression depends on the interaction between the aryl hydrocarbon receptor (AhR) with Xenobiotic Responsive Elements (XREs) located in the gene promoter. In this study, we used cell culture to determine the effect of indole-3-carbinol (I3C) over cellular viability, apoptosis, cell proliferation, and mRNA levels of and In addition, patients' samples were used to determine the mRNA levels of and genes. We found that I3C promotes the activation of AhR and decreases cell proliferation, possibly through mRNA induction, which would result in the ubiquitination of HPV E7. Since there is a strong requirement for selective and cost-effective cancer treatments, natural AhR ligands such as I3C could represent a novel strategy for cancer treatment.
ISSN:1467-3045
1467-3037
1467-3045
DOI:10.3390/cimb44050139