PI3K/AKT/mTOR signaling transduction pathway and targeted therapies in cancer

A Glaviano, ASC Foo, HY Lam, KCH Yap, W Jacot… - Molecular cancer, 2023 - Springer
Abstract The PI3K/AKT/mTOR (PAM) signaling pathway is a highly conserved signal
transduction network in eukaryotic cells that promotes cell survival, cell growth, and cell …

[HTML][HTML] Small molecules in targeted cancer therapy: advances, challenges, and future perspectives

L Zhong, Y Li, L Xiong, W Wang, M Wu… - Signal transduction and …, 2021 - nature.com
Due to the advantages in efficacy and safety compared with traditional chemotherapy drugs,
targeted therapeutic drugs have become mainstream cancer treatments. Since the first …

BTK inhibitors in the treatment of hematological malignancies and inflammatory diseases: mechanisms and clinical studies

A Alu, H Lei, X Han, Y Wei, X Wei - Journal of Hematology & Oncology, 2022 - Springer
Bruton's tyrosine kinase (BTK) is an essential component of multiple signaling pathways that
regulate B cell and myeloid cell proliferation, survival, and functions, making it a promising …

PI3K inhibitors in cancer: clinical implications and adverse effects

R Mishra, H Patel, S Alanazi, MK Kilroy… - International journal of …, 2021 - mdpi.com
The phospatidylinositol-3 kinase (PI3K) pathway is a crucial intracellular signaling pathway
which is mutated or amplified in a wide variety of cancers including breast, gastric, ovarian …

Managing toxicities of Bruton tyrosine kinase inhibitors

A Lipsky, N Lamanna - Hematology 2014, the American Society …, 2020 - ashpublications.org
Inhibition of Bruton's tyrosine kinase (BTK) has revolutionized the treatment landscape for
patients with chronic lymphocytic leukemia (CLL). By targeting this critical kinase in proximal …

Bruton tyrosine kinase inhibitors in B-cell malignancies: their use and differential features

M Shirley - Targeted oncology, 2022 - Springer
Starting with the first-in-class agent ibrutinib, the development of Bruton tyrosine kinase
(BTK) inhibitors has led to dramatic improvements in the management of B-cell …

Tirabrutinib: first approval

S Dhillon - Drugs, 2020 - Springer
Tirabrutinib (Velexbru®) is an orally administered, small molecule, Bruton's tyrosine kinase
(BTK) inhibitor being developed by Ono Pharmaceutical and its licensee Gilead Sciences for …

PI3K inhibitors in chronic lymphocytic leukemia: where do we go from here?

SS Skånland, JR Brown - Haematologica, 2022 - pmc.ncbi.nlm.nih.gov
Phosphatidylinositol 3-kinase (PI3K) inhibitors are effective in chronic lymphocytic leukemia
(CLL). However, the severe toxicity profile associated with the first-generation inhibitors …

Pathogenesis of chronic lymphocytic leukemia and the development of novel therapeutic strategies

Y Kikushige - Journal of clinical and experimental hematopathology, 2020 - jstage.jst.go.jp
Chronic lymphocytic leukemia (CLL) is the most common adult leukemia in Western
countries and is characterized by the clonal expansion of mature CD5+ B cells. There have …

Next generation BTK inhibitors in CLL: evolving challenges and new opportunities

AM Frustaci, M Deodato, G Zamprogna, R Cairoli… - Cancers, 2023 - mdpi.com
Simple Summary Chronic lymphocytic leukemia (CLL) treatment scenario is rapidly
evolving. As a consequence of longer observation, despite remarkable clinical results …