Accès ouvert
2020
article
OpenAlex
Markos L. Leggas, Xiuling Lu, Philip M. Potter, Melissa D. Howard et autres
The pre-administration of the anti-inflammatory drugs dexamethasone (DEX) and cortisone acetate reduces toxicity and enhances efficacy of anticancer agents in murine models and in human clinical trials (1–5). We previously reported on the formulation of the lipophilic dexamethasone palmitate ester (DEX-P) in …
2015
article
OpenAlex
Kimberly R. Doherty, Dominique R. Talbert, Patricia B. Trusk, Scott A. Shell et autres
us
(code pays fourni par la source)
2015
conference-abstract
OpenAlex
Dominique R. Talbert, Kimberly R. Doherty, Patricia B. Trusk, Diarmuid Martin Moran et autres
Abstract The human epidermal growth factor receptor 2 (HER2) oncogene is amplified and overexpressed in 25 to 30% of breast cancers and is associated with poor prognosis. Currently, two HER2-targeting agents have been FDA-approved for the treatment of these breast cancers: trastuzumab …
us
(code pays fourni par la source)
2015
article
OpenAlex
Kimberly R. Doherty, Dominique R. Talbert, Patricia B. Trusk, Diarmuid Martin Moran et autres
us
(code pays fourni par la source)
Accès ouvert
2014
article
OpenAlex
Dominique R. Talbert, Kimberly R. Doherty, Patricia B. Trusk, Diarmuid Martin Moran et autres
Ponatinib, a multi-targeted TKI and potent pan-ABL inhibitor, approved for the treatment of Ph + ALL and CML, was temporarily withdrawn from the U.S. market due to severe vascular adverse events. Cardiac-specific toxicities including myocardial infarction, severe congestive heart failure, and cardiac …
gb, us
(code pays fourni par la source)
2014
conference-abstract
OpenAlex
Dominique R. Talbert, Kimberly R. Doherty, Patricia B. Trusk, Diarmuid Martin Moran et autres
Abstract Although tyrosine kinase inhibitors (TKI) have greatly improved the treatment and prognosis of multiple cancer types, unexpected clinical cardiotoxicity has occurred with some of these agents that was not predicted by standard preclinical toxicity assessment methods. Since cardiotoxicity with TKI are …
us
(code pays fourni par la source)
2013
conference-abstract
OpenAlex
Dominique R. Talbert, Kimberly R. Doherty, Diarmuid Martin Moran, Robert Wappell et autres
Abstract Tyrosine Kinase Inhibitors (TKI) have greatly improved the treatment and prognosis of multiple cancer types. However unexpected clinical cardiotoxicity has been shown with some of these agents that was not wholly predicted by current preclinical toxicity assessment methods. Since cardiotoxicity with …
us
(code pays fourni par la source)
2013
article
OpenAlex
Kimberly R. Doherty, Robert L. Wappel, Dominique R. Talbert, Patricia B. Trusk et autres
us
(code pays fourni par la source)
2013
conference-abstract
OpenAlex
Dominique R. Talbert, Robert L. Wappel, Diarmuid Martin Moran, Scott A. Shell et autres
Abstract In recent years histone deacetylase inhibitors (HDACi's) have emerged as promising therapeutics for cancer. While favorable responses to HDACi's as single agents have been shown in several hematological malignancies, very little efficacy has been demonstrated in solid tumors. c-Myc (Myc), an …
us
(code pays fourni par la source)
2013
conference-abstract
OpenAlex
Kimberly R. Doherty, Robert L. Wappel, Dominique R. Talbert, Patricia B. Trusk et autres
Abstract Tyrosine kinase inhibitors (TKi) have greatly improved the treatment and prognosis of multiple cancer types. However, unexpected cardiotoxicity has arisen that was not wholly predicted by current FDA mandated pre-clinical tests. Thus a more robust tool to predict the cardiotoxic potential …
us
(code pays fourni par la source)
Accès ouvert
2013
article
OpenAlex
Dominique R. Talbert, Robert L. Wappel, Diarmuid Martin Moran, Scott A. Shell et autres
In recent years histone deacetylase inhibitors (HDACi’s) have emerged as promising therapeutics for cancer. While favorable responses to HDACi’s as single agents have been shown in several hematological malignancies, very little efficacy has been demonstrated in solid tumors. c-Myc (Myc), an oncoprotein …
us
(code pays fourni par la source)
2011
conference-abstract
OpenAlex
Dominique R. Talbert, Xiaodong Peng, Scott A. Shell, Sarah S. Bacus
Abstract miR-17∼92 is an oncogenic polycistronic cluster encoding six mature miRNAs (MIR-17, MIR-20A, MIR-18A, MIR-19A, MIR-19B, and MIR-92A). This oncogenic cluster is driven by MYC activity and is highly-expressed in many tumor types where it has been shown to promote tumorigenesis through …
us
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