[HTML][HTML] Tumor suppressor p53: Biology, signaling pathways, and therapeutic targeting

LJH Borrero, WS El-Deiry - Biochimica et Biophysica Acta (BBA)-Reviews …, 2021 - Elsevier
TP53 is the most commonly mutated gene in human cancer with over 100,000 literature
citations in PubMed. This is a heavily studied pathway in cancer biology and oncology with a …

p53 modifications: exquisite decorations of the powerful guardian

Y Liu, O Tavana, W Gu - Journal of molecular cell biology, 2019 - academic.oup.com
The last 40 years have witnessed how p53 rose from a viral binding protein to a central
factor in both stress responses and tumor suppression. The exquisite regulation of p53 …

[HTML][HTML] Role of p53 in breast cancer progression: An insight into p53 targeted therapy

C Marvalim, A Datta, SC Lee - Theranostics, 2023 - ncbi.nlm.nih.gov
The transcription factor p53 is an important regulator of a multitude of cellular processes. In
the presence of genotoxic stress, p53 is activated to facilitate DNA repair, cell cycle arrest …

MDM2, MDMX and p53 in oncogenesis and cancer therapy

M Wade, YC Li, GM Wahl - Nature Reviews Cancer, 2013 - nature.com
The MDM2 and MDMX (also known as HDMX and MDM4) proteins are deregulated in many
human cancers and exert their oncogenic activity predominantly by inhibiting the p53 tumour …

Drugging the p53 pathway: understanding the route to clinical efficacy

KH Khoo, CS Verma, DP Lane - Nature reviews Drug discovery, 2014 - nature.com
The tumour suppressor p53 is the most frequently mutated gene in human cancer, with more
than half of all human tumours carrying mutations in this particular gene. Intense efforts to …

Clinical overview of MDM2/X-targeted therapies

A Burgess, KM Chia, S Haupt, D Thomas… - Frontiers in …, 2016 - frontiersin.org
MDM2 and MDMX are the primary negative regulators of p53, which under normal
conditions maintain low intracellular levels of p53 by targeting it to the proteasome for rapid …

PAINS in the assay: chemical mechanisms of assay interference and promiscuous enzymatic inhibition observed during a sulfhydryl-scavenging HTS

JL Dahlin, JWM Nissink, JM Strasser… - Journal of medicinal …, 2015 - ACS Publications
Significant resources in early drug discovery are spent unknowingly pursuing artifacts and
promiscuous bioactive compounds, while understanding the chemical basis for these …

Inhibition of p53 inhibitors: progress, challenges and perspectives

G Sanz, M Singh, S Peuget… - Journal of molecular cell …, 2019 - academic.oup.com
Abstract p53 is the major tumor suppressor and the most frequently inactivated gene in
cancer. p53 could be disabled either by mutations or by upstream negative regulators …

The roles of MDM2 and MDMX in cancer

O Karni-Schmidt, M Lokshin… - Annual Review of …, 2016 - annualreviews.org
For more than 25 years, MDM2 and its homolog MDMX (also known as MDM4) have been
shown to exert oncogenic activity. These two proteins are best understood as negative …

p53 as a target for the treatment of cancer

MJ Duffy, NC Synnott, PM McGowan, J Crown… - Cancer treatment …, 2014 - Elsevier
Abstract TP53 (p53) is the most frequently mutated gene in cancer, being altered in
approximately 50% of human malignancies. In most, if not all, cancers lacking mutation, wild …