[HTML][HTML] Tumor microenvironment and immune evasion in head and neck squamous cell carcinoma

A Elmusrati, J Wang, CY Wang - International journal of oral science, 2021 - nature.com
Head and neck squamous cell carcinoma (HNSCC), an aggressive malignancy, is
characterized by high morbidity and low survival rates with limited therapeutic options …

Advances in targeting 'undruggable'transcription factors with small molecules

MJ Henley, AN Koehler - Nature Reviews Drug Discovery, 2021 - nature.com
Transcription factors (TFs) represent key biological players in diseases including cancer,
autoimmunity, diabetes and cardiovascular disease. However, outside nuclear receptors …

Synthesis and applications of mirror-image proteins

K Harrison, AS Mackay, L Kambanis… - Nature Reviews …, 2023 - nature.com
The homochirality of biomolecules in nature, such as DNA, RNA, peptides and proteins, has
played a critical role in establishing and sustaining life on Earth. This chiral bias has also …

[HTML][HTML] Apoptosis as anticancer mechanism: function and dysfunction of its modulators and targeted therapeutic strategies

G Pistritto, D Trisciuoglio, C Ceci, A Garufi… - Aging (albany …, 2016 - ncbi.nlm.nih.gov
Apoptosis is a form of programmed cell death that results in the orderly and efficient removal
of damaged cells, such as those resulting from DNA damage or during development …

The p53 pathway: origins, inactivation in cancer, and emerging therapeutic approaches

AC Joerger, AR Fersht - Annual review of biochemistry, 2016 - annualreviews.org
Inactivation of the transcription factor p53, through either direct mutation or aberrations in
one of its many regulatory pathways, is a hallmark of virtually every tumor. In recent years …

Discovery of MD-224 as a first-in-class, highly potent, and efficacious proteolysis targeting chimera murine double minute 2 degrader capable of achieving complete …

Y Li, J Yang, A Aguilar, D McEachern… - Journal of medicinal …, 2018 - ACS Publications
Human murine double minute 2 (MDM2) protein is a primary endogenous cellular inhibitor
of the tumor suppressor p53 and has been pursued as an attractive cancer therapeutic …

Systematic identification of genomic markers of drug sensitivity in cancer cells

MJ Garnett, EJ Edelman, SJ Heidorn, CD Greenman… - Nature, 2012 - nature.com
Clinical responses to anticancer therapies are often restricted to a subset of patients. In
some cases, mutated cancer genes are potent biomarkers for responses to targeted agents …

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 …

Small-molecule inhibitors of the MDM2–p53 protein–protein interaction (MDM2 Inhibitors) in clinical trials for cancer treatment: miniperspective

Y Zhao, A Aguilar, D Bernard… - Journal of medicinal …, 2015 - ACS Publications
Design of small-molecule inhibitors (MDM2 inhibitors) to block the MDM2–p53 protein–
protein interaction has been pursued as a new cancer therapeutic strategy. In recent years …