Fragile X syndrome and targeted treatment trials

R Hagerman, J Lauterborn, J Au… - Modeling fragile X …, 2012 - Springer
Work in recent years has revealed an abundance of possible new treatment targets for
fragile X syndrome (FXS). The use of animal models, including the fragile X knockout mouse …

Dual targeting of phosphoinositide 3-kinase and mammalian target of rapamycin using NVP-BEZ235 as a novel therapeutic approach in human ovarian carcinoma

C Santiskulvong, GE Konecny, M Fekete… - Clinical Cancer …, 2011 - AACR
Purpose: This study evaluates the effect of dual PI3K and mTOR inhibition using NVP-
BEZ235 in preclinical models of ovarian cancer as a potential novel therapeutic strategy …

Mechanisms of resistance to mTOR inhibitors

L Formisano, F Napolitano, R Rosa, V D'Amato… - Critical reviews in …, 2020 - Elsevier
In several tumors the PI3K/AKT/mTOR pathway is frequently disrupted, an event that results
in uncontrolled cell proliferation and tumor growth. Through the years, several compounds …

[PDF][PDF] Future directions of next-generation novel therapies, combination approaches, and the development of personalized medicine in myeloma

CS Mitsiades, FE Davies, JP Laubach… - Journal of clinical …, 2011 - academia.edu
Despite tangible progress in recent years, substantial therapeutic challenges remain in
multiple myeloma (MM), particularly for patients at high risk for early relapse or death and for …

A novel PI3K/mTOR dual inhibitor, CMG002, overcomes the chemoresistance in ovarian cancer

HJ Choi, JH Heo, JY Park, JY Jeong, HJ Cho… - Gynecologic …, 2019 - Elsevier
Objective Ovarian cancer is the leading cause of gynecologic-related mortality worldwide.
Despite successful initial treatment, overall survival rates are very low because tumors …

Active kinase profiling, genetic and pharmacological data define mTOR as an important common target in triple-negative breast cancer

JC Montero, A Esparís-Ogando, MF Re-Louhau… - Oncogene, 2014 - nature.com
Triple-negative breast cancer (TNBC) is an aggressive form of breast cancer. Despite
response to chemotherapy, relapses are frequent and resistance to available treatments is …

[HTML][HTML] The interaction of bortezomib with multidrug transporters: implications for therapeutic applications in advanced multiple myeloma and other neoplasias

R O'Connor, MG Ooi, J Meiller, J Jakubikova… - Cancer chemotherapy …, 2013 - Springer
Purpose Bortezomib is an important agent in multiple myeloma treatment, but resistance in
cell lines and patients has been described. The main mechanisms of resistance described in …

Induction of autophagy by PI3K/MTOR and PI3K/MTOR/BRD4 inhibitors suppresses HIV-1 replication

GR Campbell, RS Bruckman, SD Herns, S Joshi… - Journal of Biological …, 2018 - ASBMB
In this study, we investigated the effects of the dual phosphatidylinositol 3-
kinase/mechanistic target of rapamycin (PI3K/MTOR) inhibitor dactolisib (NVP-BEZ235), the …

The PP242 mammalian target of rapamycin (mTOR) inhibitor activates extracellular signal-regulated kinase (ERK) in multiple myeloma cells via a target of rapamycin …

B Hoang, A Benavides, Y Shi, Y Yang, P Frost… - Journal of Biological …, 2012 - ASBMB
Activation of PI3-K-AKT and ERK pathways is a complication of mTOR inhibitor therapy.
Newer mTOR inhibitors (like pp242) can overcome feedback activation of AKT in multiple …

The susceptibility of trypanosomatid pathogens to PI3/mTOR kinase inhibitors affords a new opportunity for drug repurposing

R Diaz-Gonzalez, FM Kuhlmann… - PLoS neglected …, 2011 - journals.plos.org
Background Target repurposing utilizes knowledge of “druggable” targets obtained in one
organism and exploits this information to pursue new potential drug targets in other …