Targeting cell cycle regulation in cancer therapy
S Diaz-Moralli, M Tarrado-Castellarnau… - Pharmacology & …, 2013 - Elsevier
Cell proliferation is an essential mechanism for growth, development and regeneration of
eukaryotic organisms; however, it is also the cause of one of the most devastating diseases …
eukaryotic organisms; however, it is also the cause of one of the most devastating diseases …
Current advances of tubulin inhibitors as dual acting small molecules for cancer therapy
KE Arnst, S Banerjee, H Chen, S Deng… - Medicinal research …, 2019 - Wiley Online Library
Microtubule (MT)‐targeting agents are highly successful drugs as chemotherapeutic agents,
and this is attributed to their ability to target MT dynamics and interfere with critical cellular …
and this is attributed to their ability to target MT dynamics and interfere with critical cellular …
Lanatoside C induces G2/M cell cycle arrest and suppresses cancer cell growth by attenuating MAPK, Wnt, JAK-STAT, and PI3K/AKT/mTOR signaling pathways
Cardiac glycosides (CGs) are a diverse family of naturally derived compounds having a
steroid and glycone moiety in their structures. CG molecules inhibit the α-subunit of …
steroid and glycone moiety in their structures. CG molecules inhibit the α-subunit of …
Kinase inhibitors of marine origin
The ocean occupies three-fourths of the Earth's surface and hosts approximately 80% of all
living species. In fact, some areas of the sea such as coral reefs possess a biodiversity …
living species. In fact, some areas of the sea such as coral reefs possess a biodiversity …
Structural insights of cyclin dependent kinases: implications in design of selective inhibitors
There are around 20 Cyclin-dependent kinases (CDKs) known till date, and various
research groups have reported their role in different types of cancer. The X-ray structures of …
research groups have reported their role in different types of cancer. The X-ray structures of …
Peruvoside targets apoptosis and autophagy through MAPK Wnt/β-catenin and PI3K/AKT/mTOR signaling pathways in human cancers
Aim To investigate the cytotoxic effect of Peruvoside and mechanism of action in human
cancers. Main methods Cell viability was measured by MTT assay and the cell cycle arrest …
cancers. Main methods Cell viability was measured by MTT assay and the cell cycle arrest …
Insights on structural characteristics and ligand binding mechanisms of CDK2
Y Li, J Zhang, W Gao, L Zhang, Y Pan, S Zhang… - International journal of …, 2015 - mdpi.com
Cyclin-dependent kinase 2 (CDK2) is a crucial regulator of the eukaryotic cell cycle.
However it is well established that monomeric CDK2 lacks regulatory activity, which needs …
However it is well established that monomeric CDK2 lacks regulatory activity, which needs …
Marine-derived lead fascaplysin: pharmacological activity, total synthesis, and structural modification
C Wang, S Wang, H Li, Y Hou, H Cao, H Hua, D Li - Marine Drugs, 2023 - mdpi.com
Fascaplysin is a planar structure pentacyclic alkaloid isolated from sponges, which can
effectively induce the apoptosis of cancer cells. In addition, fascaplysin has diverse …
effectively induce the apoptosis of cancer cells. In addition, fascaplysin has diverse …
Selective CDK9 inhibition by natural compound toyocamycin in cancer cells
Simple Summary By combining drug screens, transcriptomic studies, and in vitro assays, our
study identified the natural product toyocamycin as a potent and selective CDK9 inhibitor …
study identified the natural product toyocamycin as a potent and selective CDK9 inhibitor …
A survey of marine natural compounds and their derivatives with anti-cancer activity reported in 2011
Cancer continues to be a major public health problem despite the efforts that have been
made in the search for novel drugs and treatments. The current sources sought for the …
made in the search for novel drugs and treatments. The current sources sought for the …