Genome-wide screen identifies cullin-RING ligase machinery required for lenalidomide-dependent CRL4CRBN activity

QL Sievers, JA Gasser, GS Cowley… - Blood, The Journal …, 2018 - ashpublications.org
Lenalidomide mediates the ubiquitination and degradation of Ikaros family zinc finger
protein 1 (IKZF1), IKZF3, and casein kinase 1α (CK1α) by facilitating their interaction with …

The landscape of signaling pathways and proteasome inhibitors combinations in multiple myeloma

T Paradzik, C Bandini, E Mereu, M Labrador, E Taiana… - Cancers, 2021 - mdpi.com
Simple Summary In the last decade, proteasome inhibitors (PIs) have become a standard for
the treatment of multiple myeloma (MM). As a consequence of the pleiotropic effects of PIs …

Emerging protein kinase inhibitors for the treatment of multiple myeloma

J Lind, F Czernilofsky, S Vallet… - Expert Opinion on …, 2019 - Taylor & Francis
Introduction: Significant advances have been made during the last two decades in terms of
new therapeutic options but also of innovative approaches to diagnosis and management of …

Development of photolenalidomide for cellular target identification

Z Lin, Y Amako, F Kabir, HA Flaxman… - Journal of the …, 2022 - ACS Publications
The thalidomide analogue lenalidomide (Len) is a clinical therapeutic that alters the
substrate engagement of cereblon (CRBN), a substrate receptor for the CRL4 E3 ubiquitin …

Redefining CD56 as a biomarker and therapeutic target in multiple myeloma

F Cottini, J Rodriguez, T Hughes, N Sharma… - Molecular Cancer …, 2022 - AACR
Multiple myeloma cells aberrantly express surface antigens compared with normal plasma
cells. Among others, CD56 is present at variable levels in approximately 70% of patients …

RSK2 protects human breast cancer cells under endoplasmic reticulum stress through activating AMPKα2-mediated autophagy

LY Li, XS Chen, KS Wang, YD Guan, XC Ren, DS Cao… - Oncogene, 2020 - nature.com
Autophagy can protect stressed cancer cell by degradation of damaged proteins and
organelles. However, the regulatory mechanisms behind this cellular process remain …

[HTML][HTML] Kinase inhibitors as potential agents in the treatment of multiple myeloma

HN Abramson - Oncotarget, 2016 - ncbi.nlm.nih.gov
Recent years have witnessed a dramatic increase in the number of therapeutic options
available for the treatment of multiple myeloma (MM)-from immunomodulating agents to …

Epigenetic repression of miR‐375 is the dominant mechanism for constitutive activation of the PDPK 1/RPS 6 KA 3 signalling axis in multiple myeloma

S Tatekawa, Y Chinen, M Ri, T Narita… - British Journal of …, 2017 - Wiley Online Library
Cytogenetic/molecular heterogeneity is the hallmark of multiple myeloma (MM). However,
we recently showed that the serine/threonine kinase PDPK 1 and its substrate RPS 6 KA 3 …

RSK2 promotes melanoma cell proliferation and vemurafenib resistance via upregulating cyclin D1

HZ Wu, LY Li, SL Jiang, YZ Li, XM Shi… - Frontiers in …, 2022 - frontiersin.org
BRAF inhibitors are commonly used in targeted therapies for melanoma patients harboring
BRAFV600E mutant. Despite the benefit of vemurafenib therapy, acquired resistance during …

A short peptide LINC00665_18aa encoded by lncRNA LINC00665 suppresses the proliferation and migration of osteosarcoma cells through the regulation of the …

J Pan, M Liu, X Duan, D Wang - Plos one, 2023 - journals.plos.org
Long noncoding RNAs (lncRNAs) encompass short open reading frames (sORFs) that can
be translated into small peptides. Here, we investigated the encoding potential of lncRNA …