CDK9 inhibitors in multiple myeloma: a review of progress and perspectives

J Borowczak, K Szczerbowski, N Ahmadi, Ł Szylberg - Medical oncology, 2022 - Springer
Currently, multiple myeloma is not yet considered a curable disease. Despite the recent
advances in therapy, the average patient lifespan is still unsatisfactory. Recently, CDK9 …

[HTML][HTML] TG02, an oral CDK9-inhibitor, in combination with carfilzomib demonstrated objective responses in carfilzomib refractory multiple myeloma patients

CC Hofmeister, JG Berdeja, DH Vesole… - Blood, 2015 - Elsevier
Introduction: TG02 is an orally-bioavailable, multikinase inhibitor where the primary
mechanism of action is through CDK9-dependent depletion of oncoproteins such as Mcl-1 …

CDK5 inhibition in vitro and in vivo induces cell death in myeloma and overcomes the obstacle of bortezomib resistance

H Tang, L Xu, X Cen, L Yang… - International …, 2020 - spandidos-publications.com
The emergence of new drugs is a major feature of the treatment history of multiple myeloma
(MM), which also reflects the current incurability of MM. As a unique member of cyclin …

Novel therapeutics in multiple myeloma

AK Stewart - Hematology, 2012 - Taylor & Francis
Most myeloma patients still experience recurrent relapse and eventually become resistant
and/or intolerant of effective agents such as corticosteroids, alkylating agents, immune …

[PDF][PDF] Level of cdk5 expression predicts the survival of relapsed multiple myeloma patients

Z Levacque, JL Rosales, KY Lee - Cell Cycle, 2012 - Taylor & Francis
* Correspondence to: Ki-Young Lee; Email: kylee@ ucalgary. ca Submitted: 07/30/12;
Accepted: 08/20/12 http://dx. doi. org/10.4161/cc. 21886 investigate the link between the …

Discovery of novel and orally bioavailable CDK 4/6 inhibitors with high kinome selectivity, low toxicity and long-acting stability for the treatment of multiple myeloma

K Yuan, W Kuang, W Chen, M Ji, W Min, Y Zhu… - European Journal of …, 2022 - Elsevier
Multiple myeloma (MM) ranks second in malignant hematopoietic cancers, and the most
common anti-MM drugs easily generate resistance. CDK4/6 have been validated to play …

Novel targets for the treatment of relapsing multiple myeloma

N Giuliani, F Accardi, V Marchica… - Expert Review of …, 2019 - Taylor & Francis
Introduction: Multiple myeloma (MM) is characterized by the high tendency to relapse and
develop drug resistance. Areas covered: This review focused on the main novel targets …

Phase I and pharmacologic study of SNS-032, a potent and selective Cdk2, 7, and 9 inhibitor, in patients with advanced chronic lymphocytic leukemia and multiple …

WG Tong, R Chen, W Plunkett, D Siegel… - Journal of clinical …, 2010 - ascopubs.org
Purpose SNS-032 is a highly selective and potent inhibitor of cyclin-dependent kinases
(Cdks) 2, 7, and 9, with in vitro growth inhibitory effects and ability to induce apoptosis in …

Potent antimyeloma activity of a novel ERK5/CDK inhibitor

S Álvarez-Fernández, MJ Ortiz-Ruiz, T Parrott… - Clinical cancer …, 2013 - AACR
Purpose: To analyze the antimyeloma potential of TG02, an ERK5/CDK inhibitory drug.
Experimental Design: Utilizing different multiple myeloma cell lines we determined the effect …

Carfilzomib plus dexamethasone in patients with relapsed and refractory multiple myeloma: a retro‐prospective observational study

ML Del Giudice, A Gozzetti, E Antonioli… - European Journal of …, 2022 - Wiley Online Library
Objective We investigate safety and efficacy in common clinical practice of the combination
of carfilzomib and dexamethasone (Kd56) approved for the ENDEAVOR trial for the …