Author

Cheril Tapia‐Rojas

Fundación Ciencia and VidaORCID 0000-0002-7084-0318Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Research Focus:cancer & tumor microenvironment· 1 Research Focus:cell type annotation· 1 Research Focus:differential expression· 1 Organism:human· 1 Assay:imaging· 1 Assay:metabolomics· 1 Organism:mouse· 1

Frequent Co-Authors

Claudia JaraiD· 2 shared Alejandra Aránguiz· 1 shared Alejandro GodoyiD· 1 shared Alejandro Pinilla· 1 shared Alejandro San MartíniD· 1 shared Alfonso GonzáleziD· 1 shared Andrea SozaiD· 1 shared Ariel Vivero· 1 shared

Activity by Year

2025-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 25 mutual co-author links

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2 shared papersCell Biology

Claudia JaraORCID

Mutual co-authors in cluster

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2 papers

Recent·Most cited

Galectin-8 regulates primary cilium in hypothalamic neurons through anL-type calcium channel/Aurora kinaseA/HDAC6 pathway impacting body energy balance

Cristian Herrera-Cid, María Paz Hernández‐Cáceres, Daniela Rodrigues Pinto, Alejandra Aránguiz, Francisca Pérez-Molina, Ariel Vivero, Daniela Cortés-Díaz, Claudia Jara, Sofía Espinoza, Andrea Soza, Cheril Tapia‐Rojas, Bredford Kerr, Eugenia Morselli, Alfonso González

This study shows Gal-8 regulates primary cilium structure and leptin signaling in hypothalamic neurons via L-type calcium channels and the Aurora kinase A/HDAC6 pathway, affecting energy balance and glucose homeostasis.

bioRxiv · Apr 16, 2026 · PreprintCell Biology

Metabolic Adaptations of Prostate Cancer Cells Under Chronic Fructose Stimulation

Carolina E. Echeverría, Vanessa I. Oyarzún, Claudia Jara, Emilia Flores-Faúndez, Catalina Ramírez, Verónica A. Torres-Estay, Cheril Tapia‐Rojas, Jorge Díaz, Manuel F. Meneses, Jorge Cancino, Alejandro Pinilla, Alejandro San Martín, Spencer R. Rosario, Alejandro Godoy

This study examines how chronic fructose exposure alters metabolism in prostate cancer cells, revealing cell-type-specific metabolic shifts and identifying Glut-5 and lipid pathways as potential therapeutic targets.

bioRxiv · Jul 7, 2025 · PreprintCell Biology