Targeting telomerase for its advent in cancer therapeutics

S Bajaj, MS Kumar, GJ Peters… - Medicinal Research …, 2020 - Wiley Online Library
Telomerase has emerged as an important primary target in anticancer therapy. It is a
distinctive reverse transcriptase enzyme, which extends the length of telomere at the 3 …

Covalent binding design strategy: A prospective method for discovery of potent targeted anticancer agents

L Wang, J Zhao, Y Yao, C Wang, J Zhang, X Shu… - European journal of …, 2017 - Elsevier
Cancer remains the most serious disease that threatens human health. Molecularly targeted
cancer therapies, specifically small-molecule protein kinase inhibitors, form an important …

Self-optimisation of the final stage in the synthesis of EGFR kinase inhibitor AZD9291 using an automated flow reactor

N Holmes, GR Akien, AJ Blacker… - Reaction Chemistry & …, 2016 - pubs.rsc.org
Self-optimising flow reactors combine online analysis with evolutionary feedback algorithms
to rapidly achieve optimum conditions. This technique has been applied to the final bond …

Recent advances in cancer therapeutics

N Chessum, K Jones, E Pasqua, M Tucker - Progress in medicinal …, 2015 - Elsevier
In the past 20 years, cancer therapeutics has undergone a paradigm shift away from the
traditional cytotoxic drugs towards the targeting of proteins intimately involved in driving the …

The potential of panHER inhibition in cancer

X Wang, KM Batty, PJ Crowe, D Goldstein… - Frontiers in …, 2015 - frontiersin.org
Purpose: Hyper-activation of the HER (erbB) family receptors, HER 1-4, leads to up-
regulation of the three vital signaling pathways: mitogen activated protein kinase …

Secondary resistant mutations to small molecule inhibitors in cancer cells

AB Hamid, RC Petreaca - Cancers, 2020 - mdpi.com
Secondary resistant mutations in cancer cells arise in response to certain small molecule
inhibitors. These mutations inevitably cause recurrence and often progression to a more …

Inhibitory effect of 1, 4, 5, 6-tetrahydroxy-7, 8-diprenylxanthone against NSCLC with L858R/T790M/C797S mutant EGFR

J Wang, Y Wang, S Zhang, Y Qu, R Zhang, X Wang… - Scientific Reports, 2024 - nature.com
Epidermal growth factor receptor (EGFR)-activating mutations are critical factors in the
development of EGFR-driven non-small-cell lung cancer (NSCLC), and molecular targeted …

Inhibiting epidermal growth factor receptor at a distance

JKL Sinclair, EV Denton… - Journal of the American …, 2014 - ACS Publications
The epidermal growth factor receptor (EGFR) tyrosine kinase is implicated in a large number
of human cancers. Most EGFR inhibitors target the extracellular, growth factor-binding …

Re-treatment with EGFR-TKIs in NSCLC patients who developed acquired resistance

WS Wu, YM Chen - Journal of Personalized Medicine, 2014 - mdpi.com
In the era of personalized medicine, epidermal growth factor receptor (EGFR) inhibition with
tyrosine kinase inhibitor (TKI) has been a mainstay of treatment for non-small cell lung …

The changing world of oncology drug development—a global pharmaceutical company's perspective

S Galbraith - Chinese Clinical Oncology, 2014 - cco.amegroups.org
Recent approvals for oncology drugs have seen an increasing proportion directed to specific
genetic targets identified with an associated companion diagnostic test. In addition, there is …