[HTML][HTML] MDM2/X inhibitors under clinical evaluation: perspectives for the management of hematological malignancies and pediatric cancer

V Tisato, R Voltan, A Gonelli, P Secchiero… - Journal of hematology & …, 2017 - Springer
The two murine double minute (MDM) family members MDM2 and MDMX are at the center
of an intense clinical assessment as molecular target for the management of cancer. Indeed …

[HTML][HTML] p53 and metabolism: from mechanism to therapeutics

FM Simabuco, MG Morale, ICB Pavan, AP Morelli… - Oncotarget, 2018 - ncbi.nlm.nih.gov
The tumor cell changes itself and its microenvironment to adapt to different situations,
including action of drugs and other agents targeting tumor control. Therefore, metabolism …

The role of autophagy in targeted therapy for acute myeloid leukemia

W Du, A Xu, Y Huang, J Cao, H Zhu, B Yang, X Shao… - Autophagy, 2021 - Taylor & Francis
Although molecular targeted therapies have recently displayed therapeutic effects in acute
myeloid leukemia (AML), limited response and acquired resistance remain common …

Cell survival and cell death at the intersection of autophagy and apoptosis: Implications for current and future cancer therapeutics

N Bata, NDP Cosford - ACS pharmacology & translational science, 2021 - ACS Publications
Autophagy and apoptosis are functionally distinct mechanisms for cytoplasmic and cellular
turnover. While these two pathways are distinct, they can also regulate each other, and …

[HTML][HTML] Resistance mechanisms to inhibitors of p53-MDM2 interactions in cancer therapy: can we overcome them?

L Haronikova, O Bonczek, P Zatloukalova… - Cellular & molecular …, 2021 - Springer
Since the discovery of the first MDM2 inhibitors, we have gained deeper insights into the
cellular roles of MDM2 and p53. In this review, we focus on MDM2 inhibitors that bind to the …

Therapeutics targeting Bcl-2 in hematological malignancies

A Ruefli-Brasse, JC Reed - Biochemical Journal, 2017 - portlandpress.com
Members of the B-cell lymphoma 2 (BCL-2) gene family are attractive targets for cancer
therapy as they play a key role in promoting cell survival, a long-since established hallmark …

[HTML][HTML] Interruption of p53-MDM2 interaction by Nutlin-3a in human lymphoma cell models initiates a cell-dependent global effect on transcriptome and proteome …

K Psatha, L Kollipara, E Drakos, E Deligianni… - Cancers, 2023 - mdpi.com
Simple Summary The activation of wild-type p53 protein in human lymphoma is a promising
therapeutic strategy. A precise interruption of a protein–protein interaction, such as the p53 …

CopA3 peptide inhibits MDM2-p53 complex stability in colorectal cancers and activates p53 mediated cell death machinery

DK Dey, C Sharma, Y Vadlamudi, SC Kang - Life Sciences, 2023 - Elsevier
The diverse expression patterns of the tumor suppressor p53 in cancer cells reflect the
regulatory efficiency of multiple cellular pathways. By contrast, many human tumors are …

[HTML][HTML] Pharmacological activation of wild-type p53 in the therapy of leukemia

K Kojima, J Ishizawa, M Andreeff - Experimental hematology, 2016 - Elsevier
Highlights•MDM2 and MDMX are direct, negative regulators of the tumor suppressor
p53.•MDM2 and MDMX represent important therapeutic targets in leukemias.•MDM2 …

p53-Mdm2 interaction inhibitors as novel nongenotoxic anticancer agents

SK Nayak, GL Khatik, R Narang… - Current cancer drug …, 2018 - ingentaconnect.com
Background: Cancer is a major global health problem with high mortality rate. Most of the
clinically used anticancer agents induce apoptosis through genotoxic stress at various …