The interactions of docetaxel with tumor microenvironment
R Gupta, MM Kadhim, AT Jalil, MQ Alasheqi… - International …, 2023 - Elsevier
There are several interactions within the tumor microenvironment (TME) that affect the
response of cancer cells to therapy. There are also a large number of cells and secretions in …
response of cancer cells to therapy. There are also a large number of cells and secretions in …
A review of progress in o-aminobenzamide-based HDAC inhibitors with dual targeting capabilities for cancer therapy
WX Zhang, J Huang, XY Tian, YH Liu, MQ Jia… - European Journal of …, 2023 - Elsevier
Histone deacetylases, as a new class of anticancer targets, could maintain homeostasis by
catalyzing histone deacetylation and play important roles in regulating the expression of …
catalyzing histone deacetylation and play important roles in regulating the expression of …
Discovery of novel N-benzylarylamide-dithiocarbamate based derivatives as dual inhibitors of tubulin polymerization and LSD1 that inhibit gastric cancers
XY Yuan, CH Song, XJ Liu, X Wang, MQ Jia… - European Journal of …, 2023 - Elsevier
In this work, N-benzylarylamide-dithiocarbamate based derivatives were designed,
synthesized, and their biological activities as anticancer agents were explored. Some of the …
synthesized, and their biological activities as anticancer agents were explored. Some of the …
Discovery of novel coumarin-indole derivatives as tubulin polymerization inhibitors with potent anti-gastric cancer activities
J Song, YF Guan, WB Liu, CH Song, XY Tian… - European Journal of …, 2022 - Elsevier
Novel coumarin-indole derivatives were designed, synthesized and evaluated as tubulin
polymerization inhibitors targeting the colchicine binding site. Among these compounds …
polymerization inhibitors targeting the colchicine binding site. Among these compounds …
Design and synthesis of new trimethoxylphenyl-linked combretastatin analogues loaded on diamond nanoparticles as a panel for ameliorated solubility and …
I Zaki, AMY Moustafa, BY Beshay… - Journal of enzyme …, 2022 - Taylor & Francis
A new series of vinyl amide-, imidazolone-, and triazinone-linked combretastatin A-4
analogues have been designed and synthesised. These compounds have been evaluated …
analogues have been designed and synthesised. These compounds have been evaluated …
An update on the recent advances and discovery of novel tubulin colchicine binding inhibitors
H Weng, J Li, H Zhu, KF Carver Wong… - Future Medicinal …, 2023 - Future Science
Microtubules, formed by α-and β-tubulin heterodimer, are considered as a major target to
prevent the proliferation of tumor cells. Microtubule-targeted agents have become …
prevent the proliferation of tumor cells. Microtubule-targeted agents have become …
[HTML][HTML] The microtubule cytoskeleton: An old validated target for novel therapeutic drugs
L Lafanechère - Frontiers in Pharmacology, 2022 - frontiersin.org
Compounds targeting microtubules are widely used in cancer therapy with a proven efficacy.
However, because they also target non-cancerous cells, their administration leads to …
However, because they also target non-cancerous cells, their administration leads to …
Indazole-based microtubule-targeting agents as potential candidates for anticancer drugs discovery
Tremendous research is focused on developing novel drug candidates targeting
microtubules to inhibit their function in several cellular processes, including cell division. In …
microtubules to inhibit their function in several cellular processes, including cell division. In …
Recent advances on the structural modification of parthenolide and its derivatives as anticancer agents
LIU Xingchen, W Xiaobing - Chinese Journal of Natural Medicines, 2022 - Elsevier
Parthenolide (PTL) is a sesquiterpene lactone derived from medicinal plant feverfew
(Tanacetum parthenium). Recent studies have demonstrated that it has multiple …
(Tanacetum parthenium). Recent studies have demonstrated that it has multiple …
The dual FAK-HDAC inhibitor MY-1259 displays potent activities in gastric cancers in vitro and in vivo
J Song, X Liu, YF Zhang, XY Tian, MY Deng… - Bioorganic …, 2023 - Elsevier
Epigenetic regulation and Focal adhesion kinase (FAK) are considered to be two important
targets for the development of antitumor drugs. Studies have shown that the combination of …
targets for the development of antitumor drugs. Studies have shown that the combination of …