Design, eco-friendly synthesis, molecular modeling and anticancer evaluation of thiazol-5 (4 H)-ones as potential tubulin polymerization inhibitors targeting the …

AM El-Naggar, IH Eissa, A Belal, AA El-Sayed - RSC advances, 2020 - pubs.rsc.org
In recent years, suppressing tubulin polymerization has been developed as a therapeutic
approach for cancer treatment. Thus, new derivatives based on thiazol-5 (4H)-ones have …

[HTML][HTML] Metabolic reprogramming in epithelial ovarian cancer

C Nantasupha, C Thonusin… - American journal of …, 2021 - ncbi.nlm.nih.gov
Cancer cells usually show adaptations to their metabolism that facilitate their growth,
invasiveness, and metastasis. Therefore, reprogramming the energy metabolism is one of …

Metronomic chemotherapy: anti-tumor pathways and combination with immune checkpoint inhibitors

E Muraro, L Vinante, E Fratta, A Bearz, D Höfler… - Cancers, 2023 - mdpi.com
Simple Summary Metronomic chemotherapy, a continuous administration of a lowered dose
of drugs without long breaks, is currently considered an alternative approach for the …

Human cancer-associated fibroblasts enhance glutathione levels and antagonize drug-induced prostate cancer cell death

EH Cheteh, M Augsten, H Rundqvist, J Bianchi… - Cell death & …, 2017 - nature.com
Drug resistance is a major problem in cancer therapy. A growing body of evidence
demonstrates that the tumor microenvironment, including cancer-associated fibroblasts …

The many facets of Notch signaling in breast cancer: toward overcoming therapeutic resistance

A Nandi, R Chakrabarti - Genes & development, 2020 - genesdev.cshlp.org
Breast cancer is the second leading cause of cancer-related death in women and is a
complex disease with high intratumoral and intertumoral heterogeneity. Such heterogeneity …

[HTML][HTML] Development of a new vesicular formulation for delivery of Ifosfamide: evidence from in vitro, in vivo, and in silico experiments

MR Hajinezhad, S Shahraki, Z Nikfarjam… - Arabian Journal of …, 2023 - Elsevier
Ifosfamide (IFO) is a member of the oxazaphosphorine family of alkylating drugs that exhibits
anticancer and immunoregulatory properties. The toxicity of IFO is dose-limited because of …

Cytotoxicity of trans-chalcone and licochalcone A against breast cancer cells is due to apoptosis induction and cell cycle arrest

LFB Bortolotto, FR Barbosa, G Silva… - Biomedicine & …, 2017 - Elsevier
Chalcones are precursors of flavonoids that exhibit structural heterogeneity and potential
antitumor activity. The objective of this study was to characterize the cytotoxicity of trans …

Enhanced histone H3 acetylation of the PD-L1 promoter via the COP1/c-Jun/HDAC3 axis is required for PD-L1 expression in drug-resistant cancer cells

H Wang, C Fu, J Du, H Wang, R He, X Yin, H Li… - Journal of Experimental …, 2020 - Springer
Background Drug resistance is a major obstacle to treating cancers because it desensitizes
cancer cells to chemotherapy. Recently, attention has been focused on changes in the tumor …

pH/NIR-responsive polypyrrole-functionalized fibrous localized drug-delivery platform for synergistic cancer therapy

AP Tiwari, TI Hwang, JM Oh, B Maharjan… - … applied materials & …, 2018 - ACS Publications
Localized drug-delivery systems (LDDSs) are a promising approach for cancer treatment
because they decrease systematic toxicity and enhance the therapeutic effect of the drugs …

HOXA9 transcription factor is a double-edged sword: from development to cancer progression

US Shenoy, D Adiga, F Alhedyan… - Cancer and Metastasis …, 2023 - Springer
The HOXA9 transcription factor serves as a molecular orchestrator in cancer stemness,
epithelial-mesenchymal transition (EMT), metastasis, and generation of the tumor …