[HTML][HTML] Anti-angiogenic agents for the treatment of solid tumors: potential pathways, therapy and current strategies–a review

AM Al-Abd, AJ Alamoudi, AB Abdel-Naim… - Journal of advanced …, 2017 - Elsevier
Recent strategies for the treatment of cancer, other than just tumor cell killing have been
under intensive development, such as anti-angiogenic therapeutic approach. Angiogenesis …

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 …

Targeting cancer cell integrins using gold nanorods in photothermal therapy inhibits migration through affecting cytoskeletal proteins

MRK Ali, Y Wu, Y Tang, H Xiao… - Proceedings of the …, 2017 - National Acad Sciences
Metastasis is responsible for most cancer-related deaths, but the current clinical treatments
are not effective. Recently, gold nanoparticles (AuNPs) were discovered to inhibit cancer cell …

Vascular disrupting agents in cancer therapy

R Smolarczyk, J Czapla, M Jarosz-Biej… - European Journal of …, 2021 - Elsevier
Tumor blood vessel formation is a key process for tumor expansion. Tumor vessels are
abnormal and differ from normal vessels in architecture and components. Besides oxygen …

βIII-tubulin overexpression in cancer: Causes, consequences, and potential therapies

A Kanakkanthara, JH Miller - Biochimica et Biophysica Acta (BBA)-Reviews …, 2021 - Elsevier
Class III β-tubulin (βIII-tubulin) is frequently overexpressed in human tumors and is
associated with resistance to microtubule-targeting agents, tumor aggressiveness, and poor …

Optimization of benzamide derivatives as potent and orally active tubulin inhibitors targeting the colchicine binding site

S Lin, T Du, J Zhang, D Wu, H Tian… - Journal of medicinal …, 2022 - ACS Publications
Targeting the colchicine binding site on tubulin is a promising strategy to develop cancer
therapeutics. Herein, we describe our systematic structure–activity relationship studies of …

Heterocyclic-fused pyrimidines as novel tubulin polymerization inhibitors targeting the colchicine binding site: structural basis and antitumor efficacy

S Banerjee, KE Arnst, Y Wang, G Kumar… - Journal of medicinal …, 2018 - ACS Publications
We report the design, synthesis, and biological evaluation of heterocyclic-fused pyrimidines
as tubulin polymerization inhibitors targeting the colchicine binding site with significantly …

Oxygen-and sulphur-containing heterocyclic compounds as potential anticancer agents

H Sachdeva, S Khaturia, M Saquib, N Khatik… - Applied Biochemistry …, 2022 - Springer
Oxygen-and sulphur-based heterocycles form the core structure of many biologically active
molecules as well as US FDA-approved drugs. Moreover, they possess broad range of …

Targeting tubulin-colchicine site for cancer therapy: inhibitors, antibody-drug conjugates and degradation agents

Y Duan, W Liu, L Tian, Y Mao… - Current Topics in …, 2019 - ingentaconnect.com
Microtubules are essential for the mitotic division of cells and have been an attractive target
for antitumour drugs due to the increased incidence of cancer and significant mitosis rate of …

Design, synthesis and bioevaluation of 6-aryl-1-(3, 4, 5-trimethoxyphenyl)-1H-benzo [d] imidazoles as tubulin polymerization inhibitors

R Liu, M Huang, S Zhang, L Li, M Li, J Sun, L Wu… - European Journal of …, 2021 - Elsevier
A series of new 6-aryl-1-(3, 4, 5-trimethoxyphenyl)-1H-benzo [d] imidazoles as tubulin
polymerization inhibitors targeting the colchicine-binding site were designed to restrict …