[HTML][HTML] Targeting mutant p53 for cancer therapy: Direct and indirect strategies

J Hu, J Cao, W Topatana… - … of hematology & …, 2021 - jhoonline.biomedcentral.com
TP53 is a critical tumor-suppressor gene that is mutated in more than half of all human
cancers. Mutations in TP53 not only impair its antitumor activity, but also confer mutant p53 …

Polo-like kinase 1 inhibitors in human cancer therapy: development and therapeutic potential

J Zhang, L Zhang, J Wang, L Ouyang… - Journal of medicinal …, 2022 - ACS Publications
Polo-like kinase 1 (PLK1) plays an important role in a variety of cellular functions, including
the regulation of mitosis, DNA replication, autophagy, and the epithelial–mesenchymal …

Reversible centriole depletion with an inhibitor of Polo-like kinase 4

YL Wong, JV Anzola, RL Davis, M Yoon, A Motamedi… - Science, 2015 - science.org
Centrioles are ancient organelles that build centrosomes, the major microtubule-organizing
centers of animal cells. Extra centrosomes are a common feature of cancer cells. To …

TRIM37 controls cancer-specific vulnerability to PLK4 inhibition

F Meitinger, M Ohta, KY Lee, S Watanabe, RL Davis… - Nature, 2020 - nature.com
Centrosomes catalyse the formation of microtubules needed to assemble the mitotic spindle
apparatus. Centrosomes themselves duplicate once per cell cycle, in a process that is …

[PDF][PDF] BUB1 and CENP-U, primed by CDK1, are the main PLK1 kinetochore receptors in mitosis

P Singh, ME Pesenti, S Maffini, S Carmignani… - Molecular Cell, 2021 - cell.com
Reflecting its pleiotropic functions, Polo-like kinase 1 (PLK1) localizes to various sub-cellular
structures during mitosis. At kinetochores, PLK1 contributes to microtubule attachments and …

Aurora-PLK1 cascades as key signaling modules in the regulation of mitosis

V Joukov, A De Nicolo - Science signaling, 2018 - science.org
Mitosis is controlled by reversible protein phosphorylation involving specific kinases and
phosphatases. A handful of major mitotic protein kinases, such as the cyclin B–CDK1 …

Progress in natural compounds/siRNA co-delivery employing nanovehicles for cancer therapy

M Ashrafizadeh, A Zarrabi, K Hushmandi… - ACS combinatorial …, 2020 - ACS Publications
Chemotherapy using natural compounds, such as resveratrol, curcumin, paclitaxel,
docetaxel, etoposide, doxorubicin, and camptothecin, is of importance in cancer therapy …

53BP1 and USP28 mediate p53 activation and G1 arrest after centrosome loss or extended mitotic duration

F Meitinger, JV Anzola, M Kaulich, A Richardson… - Journal of Cell …, 2016 - rupress.org
In normal human cells, centrosome loss induced by centrinone—a specific centrosome
duplication inhibitor—leads to irreversible, p53-dependent G1 arrest by an unknown …

[HTML][HTML] The role of TBK1 in cancer pathogenesis and anticancer immunity

AP Runde, R Mack, PB SJ, J Zhang - Journal of Experimental & Clinical …, 2022 - Springer
The TANK-binding kinase 1 (TBK1) is a serine/threonine kinase belonging to the non-
canonical inhibitor of nuclear factor-κB (IκB) kinase (IKK) family. TBK1 can be activated by …

[HTML][HTML] TP53 Mutations in Acute Myeloid Leukemia: Still a Daunting Challenge?

M Molica, C Mazzone, P Niscola… - Frontiers in oncology, 2021 - frontiersin.org
TP53 is a key tumor suppressor gene with protean functions associated with preservation of
genomic balance, including regulation of cellular senescence, apoptotic pathways …