A review of progress in o-aminobenzamide-based HDAC inhibitors with dual targeting capabilities for cancer therapy

WX Zhang, J Huang, XY Tian, YH Liu, MQ Jia… - European Journal of …, 2023 - Elsevier
Histone deacetylases, as a new class of anticancer targets, could maintain homeostasis by
catalyzing histone deacetylation and play important roles in regulating the expression of …

[HTML][HTML] Novel immune modulators used in hematology: impact on NK cells

S Krieg, E Ullrich - Frontiers in immunology, 2013 - frontiersin.org
There is a wide range of important pharmaceuticals used in treatment of cancer. Besides
their known effects on tumor cells, there is growing evidence for modulation of the immune …

Discovery of 7H-Pyrrolo [2, 3-d] pyrimidine Derivatives as potent hematopoietic progenitor kinase 1 (HPK1) inhibitors

F Wu, H Li, Q An, Y Sun, J Yu, W Cao, P Sun… - European Journal of …, 2023 - Elsevier
Abstract Hematopoietic progenitor kinase 1 (HPK1) is predominantly expressed in
hematopoietic cells and is a negative regulator of T cell receptor (TCR) signaling. Recent …

NF2 and canonical Hippo-YAP pathway define distinct tumor subsets characterized by different immune deficiency and treatment implications in human pleural …

H Yang, SRR Hall, B Sun, L Zhao, Y Gao, RA Schmid… - Cancers, 2021 - mdpi.com
Simple Summary It is a long-held notion that loss-of-function mutations in negative
regulators of the Hippo-YAP pathway, such as NF2, LATS1/2, have a similar potential to …

Inhibition of glycosphingolipid biosynthesis reverts multidrug resistance by differentially modulating ABC transporters in chronic myeloid leukemias

EJ Salustiano, KM da Costa, L Freire-de-Lima… - Journal of Biological …, 2020 - ASBMB
Multidrug resistance (MDR) in cancer arises from cross-resistance to structurally-and
functionally-divergent chemotherapeutic drugs. In particular, MDR is characterized by …

[HTML][HTML] NKT-like (CD3+ CD56+) cells in chronic myeloid leukemia patients treated with tyrosine kinase inhibitors

JS Almeida, P Couceiro, N López-Sejas… - Frontiers in …, 2019 - frontiersin.org
Therapy with Tyrosine Kinase Inhibitors (TKI) aiming stable deep molecular response is the
gold standard to treat Chronic Myeloid Leukemia (CML). NKT-like cells (CD3+ CD56+) …

Interferon γ is a STAT1-dependent direct inducer of BCL6 expression in imatinib-treated chronic myeloid leukemia cells

HS Madapura, N Nagy, D Ujvari, T Kallas… - Oncogene, 2017 - nature.com
Abstract B-cell CLL/lymphoma 6 (BCL6) exerts oncogenic effects in several human
hematopoietic malignancies including chronic myeloid leukemia (CML), where BCL6 …

[HTML][HTML] Killer-cell immunoglobulin-like receptor gene profile predicts good molecular response to dasatinib therapy in chronic myeloid leukemia

A Kreutzman, T Jaatinen, D Greco, E Vakkila… - Experimental …, 2012 - Elsevier
Tyrosine kinase inhibitors have greatly improved the prognosis of chronic myeloid leukemia
(CML). In addition to direct kinase inhibition, their effects can also be mediated through …

An essential role for the immune system in the mechanism of tumor regression following targeted oncogene inactivation

SC Casey, Y Li, DW Felsher - Immunologic research, 2014 - Springer
Tumors are genetically complex and can have a multitude of mutations. Consequently, it is
surprising that the suppression of a single oncogene can result in rapid and sustained tumor …

BCR:: ABL1 tyrosine kinase inhibitors hamper the therapeutic efficacy of blinatumomab in vitro

J Kauer, M Märklin, M Pflügler, S Hörner… - Journal of Cancer …, 2022 - Springer
Purpose Acute B-lymphoblastic leukemia (B-ALL) is a malignant disease characterized by
accumulation of clonal immature lymphocytes in the bone marrow and peripheral blood. The …