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 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 …
[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 …
Recent progress on microtubule degradation agents
C Zhang, M Zhao, G Wang, Y Li - Journal of Medicinal Chemistry, 2023 - ACS Publications
Targeted protein degradation (TPD) has emerged as the most promising approach for the
specific knockdown of disease-associated proteins and is achieved by exploiting the cellular …
specific knockdown of disease-associated proteins and is achieved by exploiting the cellular …
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 …
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 …
Design, synthesis, and antitumor efficacy of substituted 2-amino [1, 2, 4] triazolopyrimidines and related heterocycles as dual inhibitors for microtubule polymerization …
L Chen, Y Hu, Z Lu, Z Lin, L Li, JQ Wu… - Journal of Medicinal …, 2023 - ACS Publications
Preclinical and clinical studies have demonstrated the synergistic effect of microtubule-
targeting agents in combination with Janus kinase 2 (JAK2) inhibitors, prompting the …
targeting agents in combination with Janus kinase 2 (JAK2) inhibitors, prompting the …
Discovery of a novel stilbene derivative as a microtubule targeting agent capable of inducing cell ferroptosis
J Zhou, Y Pang, W Zhang, F OuYang… - Journal of Medicinal …, 2022 - ACS Publications
Microtubule targeting agents (MTAs) are used as clinically effective chemotherapies for
cancer treatment but might be limited by the acquired or intrinsic resistance of cancer cells to …
cancer treatment but might be limited by the acquired or intrinsic resistance of cancer cells to …
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 …