[HTML][HTML] Novel proteasome inhibitors and histone deacetylase inhibitors: progress in myeloma therapeutics

S Chhabra - Pharmaceuticals, 2017 - mdpi.com
The unfolded protein response is responsible for the detection of misfolded proteins and the
coordination of their disposal and is necessary to maintain the cellular homoeostasis …

The novel AKT inhibitor afuresertib shows favorable safety, pharmacokinetics, and clinical activity in multiple myeloma

A Spencer, SS Yoon, SJ Harrison… - Blood, The Journal …, 2014 - ashpublications.org
Abstract The PI3K/AKT pathway is constitutively active in hematologic malignancies,
providing proliferative and antiapoptotic signals and possibly contributing to drug resistance …

[HTML][HTML] Targeting the mitochondrial apoptotic pathway: a preferred approach in hematologic malignancies?

K Brinkmann, H Kashkar - Cell death & disease, 2014 - nature.com
Acquired resistance toward apoptosis represents one of the hallmarks of human cancer and
a major cause of the inefficacy of most anticancer treatment regimens. Based on its ability to …

Profiling bortezomib resistance identifies secondary therapies in a mouse myeloma model

HAF Stessman, LB Baughn, A Sarver, T Xia… - Molecular cancer …, 2013 - AACR
Multiple myeloma is a hematologic malignancy characterized by the proliferation of
neoplastic plasma cells in the bone marrow. Although the first-to-market proteasome …

[HTML][HTML] “Direct to Drug” screening as a precision medicine tool in multiple myeloma

C Bonolo de Campos, N Meurice, JL Petit… - Blood cancer …, 2020 - nature.com
Seventy-six FDA-approved oncology drugs and emerging therapeutics were evaluated in 25
multiple myeloma (MM) and 15 non-Hodgkin's lymphoma cell lines and in 113 primary MM …

Endoplasmic reticulum stress plays a pivotal role in cell death mediated by the pan-deacetylase inhibitor panobinostat in human hepatocellular cancer cells

R Montalbano, P Waldegger, K Quint, S Jabari… - Translational …, 2013 - Elsevier
Panobinostat, a pan-deacetylase inhibitor, represents a novel therapeutic option for cancer
diseases. Besides its ability to block histone deacetylases (HDACs) by promoting histone …

Noncompetitive Modulation of the Proteasome by Imidazoline Scaffolds Overcomes Bortezomib Resistance and Delays MM Tumor Growth in Vivo

TA Lansdell, MA Hurchla, J Xiang, S Hovde… - ACS chemical …, 2013 - ACS Publications
Multiple myeloma (MM) is a malignant disorder of differentiated B-cells for which standard
care involves the inhibition of the proteasome. All clinically used proteasome inhibitors …

Unfolded protein response inducers tunicamycin and dithiothreitol promote myeloma cell differentiation mediated by XBP-1

H Jiang, J Zou, H Zhang, W Fu, T Zeng… - Clinical and …, 2015 - Springer
The unfolded protein response (UPR) is an essential pathway for both normal and malignant
plasma cells to maintain endoplasmic reticulum (ER) homeostasis in response to the large …

[HTML][HTML] Novel agents for the treatment of multiple myeloma: proteasome inhibitors and immunomodulatory agents

SE Kurtin, E Bilotti - Journal of the advanced practitioner in …, 2013 - ncbi.nlm.nih.gov
The integration of novel agents into the treatment of multiple myeloma (MM) has shifted the
focus from an incurable disease to one that is chronic, with a realistic hope of someday …

[HTML][HTML] Proteasome inhibitors prevent bi-directional HER2/estrogen-receptor cross-talk leading to cell death in endocrine and lapatinib-resistant HER2+/ER+ breast …

S Thaler, M Schmidt, S Roβwag, G Thiede, A Schad… - Oncotarget, 2017 - ncbi.nlm.nih.gov
Amplification and/or overexpression of the human epidermal growth factor 2 (HER2)
oncogene occurs in about 13–15% of invasive breast cancer and triggers breast cancer cell …