Recent advances in the development of protein–protein interactions modulators: mechanisms and clinical trials

H Lu, Q Zhou, J He, Z Jiang, C Peng, R Tong… - Signal transduction and …, 2020 - nature.com
Protein–protein interactions (PPIs) have pivotal roles in life processes. The studies showed
that aberrant PPIs are associated with various diseases, including cancer, infectious …

Targeting protein–protein interactions as an anticancer strategy

AA Ivanov, FR Khuri, H Fu - Trends in pharmacological sciences, 2013 - cell.com
The emergence and convergence of cancer genomics, targeted therapies, and network
oncology have significantly expanded the landscape of protein–protein interaction (PPI) …

Targeting the ubiquitin pathway for cancer treatment

J Liu, S Shaik, X Dai, Q Wu, X Zhou, Z Wang… - Biochimica et Biophysica …, 2015 - Elsevier
Proteasome-mediated degradation is a common mechanism by which cells renew their
intracellular proteins and maintain protein homeostasis. In this process, the E3 ubiquitin …

Structure-based design of high affinity peptides inhibiting the interaction of p53 with MDM2 and MDMX

J Phan, Z Li, A Kasprzak, B Li, S Sebti, W Guida… - Journal of Biological …, 2010 - ASBMB
MDM2 and MDMX function as key regulators of p53 by binding to its N terminus, inhibiting its
transcriptional activity, and promoting degradation. MDM2 and MDMX overexpression or …

Targeting p53-MDM2-MDMX loop for cancer therapy

Q Zhang, SX Zeng, H Lu - Mutant p53 and MDM2 in Cancer, 2014 - Springer
The tumor suppressor p53 plays a central role in anti-tumorigenesis and cancer therapy. It
has been described as “the guardian of the genome”, because it is essential for conserving …

Medicinal chemistry strategies to disrupt the p53–MDM2/MDMX interaction

A Lemos, M Leao, J Soares, A Palmeira… - Medicinal research …, 2016 - Wiley Online Library
The growth inhibitory activity of p53 tumor suppressor is tightly regulated by interaction with
two negative regulatory proteins, murine double minute 2 (MDM2) and X (MDMX), which are …

Abrogating the interaction between p53 and mortalin (Grp75/HSPA9/mtHsp70) for cancer therapy: the story so far

A Elwakeel - Frontiers in Cell and Developmental Biology, 2022 - frontiersin.org
p53 is a transcription factor that activates the expression of a set of genes that serve as a
critical barrier to oncogenesis. Inactivation of p53 is the most common characteristic in …

Triapine analogues and their copper (II) complexes: Synthesis, characterization, solution speciation, redox activity, cytotoxicity, and mR2 RNR inhibition

I Besleaga, I Stepanenko, TV Petrasheuskaya… - Inorganic …, 2021 - ACS Publications
Three new thiosemicarbazones (TSCs) HL 1–HL 3 as triapine analogues bearing a redox-
active phenolic moiety at the terminal nitrogen atom were prepared. Reactions of HL 1–HL 3 …

Small-molecule inhibitors of p53-MDM2 interaction: the 2006-2010 update

M Millard, D Pathania, F Grande, S Xu… - Current …, 2011 - ingentaconnect.com
Increasing knowledge of the relationship between p53 and MDM2 has led to development of
potential small molecule inhibitors useful for clinical studies. Herein, we discuss the …

Potential Metabolite Nymphayol Isolated from Water Lily (Nymphaea stellata) Flower Inhibits MCF-7 Human Breast Cancer Cell Growth via Upregulation of Cdkn2a …

LN Al-Harbi, P Subash-Babu, MA Binobead… - Metabolites, 2020 - mdpi.com
Controlled production of cyclin dependent kinases (CDK) and stabilization of tumor
suppressor genes are the most important factors involved in preventing carcinogenesis. The …