Y. Maxuitenko

发表

Comparative Response of SC CAKI-1 Renal Tumor to Treatment with Doxorubicin HCl and Doxorubicin Orotate

G. Gorman, R. Karmali, Y. Maxuitenko, 2014 .

Vascular endothelial growth factor reduces tamoxifen efficacy and promotes metastatic colonization and desmoplasia in breast tumors.

Rongbao Li, A. Roy, F. Kern, 2008, Cancer research.

Colon Tumor Cell Growth–Inhibitory Activity of Sulindac Sulfide and Other Nonsteroidal Anti-Inflammatory Drugs Is Associated with Phosphodiesterase 5 Inhibition

H. Tinsley, B. Gary, G. Piazza, 2010, Cancer Prevention Research.

A Novel Sulindac Derivative That Does Not Inhibit Cyclooxygenases but Potently Inhibits Colon Tumor Cell Growth and Induces Apoptosis with Antitumor Activity

H. Tinsley, B. Gary, G. Piazza, 2009, Cancer Prevention Research.

Transient intervention with oltipraz protects against aflatoxin-induced hepatic tumorigenesis.

A. Muñoz, J. Groopman, T. Kensler, 1993, Cancer research.

Identification of dithiolethiones with better chemopreventive properties than oltipraz.

T. Kensler, B. Roebuck, A. Libby, 1998, Carcinogenesis.

Protection against aflatoxin B1-induced hepatic toxicity as short-term screen of cancer chemopreventive dithiolethiones.

T. Kensler, B. Roebuck, Y. Maxuitenko, 1996, Fundamental and Applied Toxicology.

Protection against Aflatoxin B1-Induced Hepatic Toxicity as a Short-Term Screen of Cancer Chemopreventive Dithiolethiones

T. Kensler, B. Roebuck, Y. Maxuitenko, 1996 .

2 – Biochemical Mechanisms and Biological Implications of the Toxicity of Aflatoxins as Related to Aflatoxin Carcinogenesis

D. Eaton, J. Groopman, B. Roebuck, 1993 .

Combinatorial treatment with carboxyamidotriazole- orotate and temozolomide in sc-implanted human LOX IMVI melanoma xenografts

G. Gorman, R. Karmali, Y. Maxuitenko, 2012 .

Rese Col Sulf Is A

B. Gary, G. Piazza, Yonghe Li, 2010 .

Evaluation of the post-initiation effects of oltipraz on aflatoxin B1-induced preneoplastic foci in a rat model of hepatic tumorigenesis.

T. Kensler, B. Roebuck, Y. Maxuitenko, 1993, Carcinogenesis.

Aflatoxin-induced Hepatic Tumorigenesis Transient Intervention with Oltipraz Protects against

J. Groopman, T. Kensler, B. Roebuck, 2006 .

Treatment with Paclitaxel Orotate and Carboxyamidotriazole Orotate in SC-Implanted OVCAR-5 Human Ovarian Tumor Xenografts

G. Gorman, R. Karmali, Y. Maxuitenko, 2013 .

From Celecoxib to a Novel Class of Phosphodiesterase 5 Inhibitors: Trisubstituted Pyrazolines as Novel Phosphodiesterase 5 Inhibitors with Extremely High Potency and Phosphodiesterase Isozyme Selectivity.

R. Hartmann, A. Abadi, G. Piazza, 2021, Journal of medicinal chemistry.

Pharmacological inhibition of ABCC3 slows tumour progression in animal models of pancreatic cancer

G. Piazza, K. Linton, V. de Laurenzi, 2019, Journal of Experimental & Clinical Cancer Research.

Novel DNA methyltransferase-1 (DNMT1) depleting anticancer nucleosides, 4′-thio-2′-deoxycytidine and 5-aza-4′-thio-2′-deoxycytidine

M. Hollingshead, W. Parker, J. Thottassery, 2014, Cancer Chemotherapy and Pharmacology.

Novel Non-Cyclooxygenase Inhibitory Derivative of Sulindac Inhibits Breast Cancer Cell Growth In Vitro and Reduces Mammary Tumorigenesis in Rats

X. Chen, H. Tinsley, B. Gary, 2023, Cancers.

Suppression of Colon Tumorigenesis in Mutant Apc Mice by a Novel PDE10 Inhibitor that Reduces Oncogenic β-Catenin

Ashley S. Lindsey, G. Piazza, H. Cooper, 2021, Cancer Prevention Research.

PDE5 and PDE10 inhibition activates cGMP/PKG signaling to block Wnt/β-catenin transcription, cancer cell growth, and tumor immunity.

M. Boyd, G. Piazza, A. Keeton, 2020, Drug discovery today.

Sorafenib is efficacious and tolerated in combination with cytotoxic or cytostatic agents in preclinical models of human non-small cell lung carcinoma

P. Vincent, Christopher A. Carter, Charles Chen, 2006, Cancer Chemotherapy and Pharmacology.

Establishment of a mammary carcinoma cell line from Syrian hamsters treated with N-methyl-N-nitrosourea.

J. Mathis, Benjamin D. L. Li, E. Orchard, 2011, Cancer letters.

Inhibition of the Lysophosphatidylinositol Transporter ABCC1 Reduces Prostate Cancer Cell Growth and Sensitizes to Chemotherapy

G. Piazza, K. Linton, M. Broggini, 2020, Cancers.

Pan-RAS inhibitors: Hitting multiple RAS isozymes with one stone.

G. Piazza, A. Keeton, D. Buchsbaum, 2022, Advances in cancer research.

Carboxyamidotriazole Orotate and Cytotoxic Chemotherapy have a Synergistic Effect on Tumor Inhibition in Glioblastoma and Colon Xenograft Mouse Models

G. Gorman, R. Karmali, Y. Maxuitenko, 2011 .

Enhancing anticancer activity of checkpoint immunotherapy by targeting RAS

G. Piazza, A. Keeton, T. Randall, 2020, MedComm.

Exploiting RAS Nucleotide Cycling as a Strategy for Drugging RAS-Driven Cancers

G. Piazza, A. Keeton, Xi Chen, 2019, International journal of molecular sciences.

A novel polyamine analog (SL-11093) inhibits growth of human prostate tumor xenografts in nude mice

L. Marton, C. Porter, N. Kisiel, 2003, Cancer Chemotherapy and Pharmacology.

Novel Pan-RAS Inhibitor ADT-007 Induces Tumor Regression in Mouse Models of GI Cancer

M. Boyd, G. Piazza, I. Babic, 2023, bioRxiv.

Cyclopropane-containing polyamine analogues are efficient growth inhibitors of a human prostate tumor xenograft in nude mice.

G. Wilding, L. Marton, D. Church, 2003, Journal of medicinal chemistry.

Abstract 2707: A novel RAS inhibitor, MCI-062, inhibits colon tumor growth in vivo and activates antitumor immunity

M. Boyd, G. Piazza, K. Berry, 2019, Immunology.

Targeting cGMP/PKG signaling for the treatment or prevention of colorectal cancer with novel sulindac derivatives lacking cyclooxygenase inhibitory activity

G. Piazza, A. Keeton, D. Buchsbaum, 2020 .

Novel sulindac derivatives for colorectal cancer chemoprevention that target cGMP phosphodiesterases to suppress Wnt/β-catenin transcriptional activity

G. Piazza, A. Keeton, Y. Maxuitenko, 2023, Cancer Insight.

Urinary taurine as a non-invasive marker of aflatoxin B1-induced hepatotoxicity: success and failure.

B. Roebuck, W. North, Y. Maxuitenko, 1997, Toxicology.