Targeting mutant p53 for efficient cancer therapy

VJN Bykov, SE Eriksson, J Bianchi… - Nature Reviews Cancer, 2018 - nature.com
The tumour suppressor gene TP53 is the most frequently mutated gene in cancer. Wild-type
p53 can suppress tumour development by multiple pathways. However, mutation of TP53 …

Exploring the multiple roles of guardian of the genome: P53

W Feroz, AMA Sheikh - Egyptian Journal of Medical Human Genetics, 2020 - Springer
Background Cells have evolved balanced mechanisms to protect themselves by initiating a
specific response to a variety of stress. The TP53 gene, encoding P53 protein, is one of the …

p53 family and cellular stress responses in cancer

J Pflaum, S Schlosser, M Müller - Frontiers in oncology, 2014 - frontiersin.org
p53 is an important tumor suppressor gene, which is stimulated by cellular stress like
ionizing radiation, hypoxia, carcinogens, and oxidative stress. Upon activation, p53 leads to …

[HTML][HTML] Mutant p53 reactivation by small molecules makes its way to the clinic

VJN Bykov, KG Wiman - FEBS letters, 2014 - Elsevier
The TP53 tumor suppressor gene is mutated in many human tumors, including common
types of cancer such as colon and ovarian cancer. This illustrates the key role of p53 as …

Structural and drug targeting insights on mutant p53

AS Gomes, H Ramos, A Inga, E Sousa, L Saraiva - Cancers, 2021 - mdpi.com
Simple Summary The tumor suppressor protein p53 is frequently mutated in human cancers,
and its reactivation represents an encouraging hope for precision anticancer therapy …

Targeted therapies in bladder cancer: an overview of in vivo research

KEM Van Kessel, TCM Zuiverloon, AR Alberts… - Nature reviews …, 2015 - nature.com
Survival of patients with muscle-invasive bladder cancer is poor and new therapies are
needed. Currently, none of the targeted agents that are approved for cancer therapy have …

2-Styryl-4-aminoquinazoline derivatives as potent DNA-cleavage, p53-activation and in vivo effective anticancer agents

XW Wei, JM Yuan, WY Huang, NY Chen, XJ Li… - European Journal of …, 2020 - Elsevier
Forty-eight analogues of CP-31398, an antitumor agent modulated the mutant p53 gene
were synthesized and their cytotoxicities against four cancer cell lines with different p-53 …

Recent synthetic approaches towards small molecule reactivators of p53

JL Silva, CGS Lima, LP Rangel, GDS Ferretti, FP Pauli… - Biomolecules, 2020 - mdpi.com
The tumor suppressor protein p53 is often called “the genome guardian” and controls the
cell cycle and the integrity of DNA, as well as other important cellular functions. Its main …

Redox sensitive cysteine residues as crucial regulators of wild-type and mutant p53 isoforms

E Butturini, G Butera, R Pacchiana, A Carcereri de Prati… - Cells, 2021 - mdpi.com
The wild-type protein p53 plays a key role in preventing the formation of neoplasms by
controlling cell growth. However, in more than a half of all cancers, the TP53 gene has …

Multikinase inhibitor motesanib enhances the antitumor effect of cisplatin in cisplatin-resistant human bladder cancer cells via apoptosis and the PI3K/Akt pathway

JN Ho, SS Byun, SE Lee, JI Youn… - Oncology …, 2019 - spandidos-publications.com
Motesanib (AMG 706) is a small organic molecule that acts as a multi-targeted tyrosine
kinase inhibitor of VEGF, PDGF and stem cell factor receptor. It exhibits a potent antitumor …