C. Cabello

发表

The experimental chemotherapeutic N6-furfuryladenosine (kinetin-riboside) induces rapid ATP depletion, genotoxic stress, and CDKN1A(p21) upregulation in human cancer cell lines.

G. Wondrak, Sarah D. Lamore, S. Ley, 2009, Biochemical pharmacology.

DCPIP (2,6-dichlorophenolindophenol) as a genotype-directed redox chemotherapeutic targeting NQO1*2 breast carcinoma

G. Wondrak, Sarah D. Lamore, C. Cabello, 2011, Free radical research.

The malondialdehyde-derived fluorophore DHP-lysine is a potent sensitizer of UVA-induced photooxidative stress in human skin cells.

K. Uchida, G. Wondrak, Sarah D. Lamore, 2010, Journal of photochemistry and photobiology. B, Biology.

Design of novel melanotropin agonists and antagonists with high potency and selectivity for human melanocortin receptors

M. Staňková, Jinfa Ying, V. Hruby, 2005, Peptides.

GLO1 overexpression in human malignant melanoma

K. Uchida, G. Wondrak, Alexandra S. Bause, 2010, Melanoma research.

Cinnamoyl-based Nrf2-activators targeting human skin cell photo-oxidative stress.

Donna D. Zhang, Zheng Sun, G. Wondrak, 2008, Free radical biology & medicine.

Antimelanoma activity of the redox dye DCPIP (2,6-dichlorophenolindophenol) is antagonized by NQO1.

G. Wondrak, Alexandra S. Bause, C. Cabello, 2009, Biochemical pharmacology.

Biological and conformational study of beta-substituted prolines in MT-II template: steric effects leading to human MC5 receptor selectivity.

C. Xiong, V. Hruby, M. Cai, 2004, The journal of peptide research : official journal of the American Peptide Society.

A Topical Zinc Ionophore Blocks Tumorigenic Progression in UV‐exposed SKH‐1 High‐risk Mouse Skin

G. Wondrak, M. Fazel, C. Cabello, 2017, Photochemistry and photobiology.

The topical antimicrobial zinc pyrithione is a heat shock response inducer that causes DNA damage and PARP-dependent energy crisis in human skin cells

G. Wondrak, Sarah D. Lamore, C. Cabello, 2010, Cell Stress and Chaperones.

An Unusual Conformation of MSH Analogues Leads to a Selective Human Melanocortin 1 Receptor Antagonist for Targeting Melanoma Cells

M. Staňková, V. Hruby, M. Cai, 2013 .

d-Penicillamine targets metastatic melanoma cells with induction of the unfolded protein response (UPR) and Noxa (PMAIP1)-dependent mitochondrial apoptosis

G. Wondrak, Sarah D. Lamore, C. Cabello, 2012, Apoptosis.

Thiostrepton is an inducer of oxidative and proteotoxic stress that impairs viability of human melanoma cells but not primary melanocytes.

G. Wondrak, Sarah D. Lamore, C. Cabello, 2012, Biochemical pharmacology.

The cinnamon-derived Michael acceptor cinnamic aldehyde impairs melanoma cell proliferation, invasiveness, and tumor growth.

G. Wondrak, Sarah D. Lamore, S. Ley, 2009, Free radical biology & medicine.

The redox antimalarial dihydroartemisinin targets human metastatic melanoma cells but not primary melanocytes with induction of NOXA-dependent apoptosis

G. Wondrak, Sarah D. Lamore, C. Cabello, 2012, Investigational New Drugs.

Repurposing the Electron Transfer Reactant Phenazine Methosulfate (PMS) for the Apoptotic Elimination of Malignant Melanoma Cells through Induction of Lethal Oxidative and Mitochondriotoxic Stress

G. Wondrak, C. Cabello, A. Hua, 2019, Cancers.

Novel cyclic templates of alpha-MSH give highly selective and potent antagonists/agonists for human melanocortin-3/4 receptors.

Paolo Grieco, Jinfa Ying, Jinfa Ying, 2002, Journal of medicinal chemistry.

An unusual conformation of γ-melanocyte-stimulating hormone analogues leads to a selective human melanocortin 1 receptor antagonist for targeting melanoma cells.

M. Staňková, V. Hruby, M. Cai, 2013, Biochemistry.

Experimental therapeutics: targeting the redox Achilles heel of cancer.

G. Wondrak, C. Cabello, W. Bair, 2007, Current opinion in investigational drugs.

Phenotypic Identification of the Redox Dye Methylene Blue as an Antagonist of Heat Shock Response Gene Expression in Metastatic Melanoma Cells

G. Wondrak, C. Cabello, S. Azimian, 2013, International journal of molecular sciences.

The tryptophan-derived endogenous arylhydrocarbon receptor ligand 6-formylindolo[3,2-b]carbazole (FICZ) is a nanomolar UVA-photosensitizer in epidermal keratinocytes

G. Wondrak, Joshua D. Williams, C. Cabello, 2014, The Journal of investigative dermatology.

d-Penicillamine targets metastatic melanoma cells with induction of the unfolded protein response (UPR) and Noxa (PMAIP1)-dependent mitochondrial apoptosis

G. Wondrak, Sarah D. Lamore, C. Cabello, 2012, Apoptosis.

Novel 3D Pharmacophore of α-MSH/γ-MSH Hybrids Leads to Selective Human MC1R and MC3R Analogues†

M. Staňková, V. Hruby, M. Cai, 2005 .

The Quinone Methide Aurin Is a Heat Shock Response Inducer That Causes Proteotoxic Stress and Noxa-dependent Apoptosis in Malignant Melanoma Cells*

G. Wondrak, Montserrat Rojo de la Vega, V. Gokhale, 2014, The Journal of Biological Chemistry.

Novel 3D pharmacophore of alpha-MSH/gamma-MSH hybrids leads to selective human MC1R and MC3R analogues.

M. Staňková, V. Hruby, M. Cai, 2005, Journal of medicinal chemistry.

Novel MTII/AGRP Hybrid Analogs that Lead to Selective Ligands for the Human Melanocortin Receptors

V. Hruby, M. Cai, K. Chandler, 2006 .

HMGB1-directed drug discovery targeting cutaneous inflammatory dysregulation.

G. Wondrak, Sarah D. Lamore, C. Cabello, 2010, Current drug metabolism.