[HTML][HTML] Angiogenic signaling pathways and anti-angiogenic therapy for cancer

ZL Liu, HH Chen, LL Zheng, LP Sun… - Signal transduction and …, 2023 - nature.com
Angiogenesis, the formation of new blood vessels, is a complex and dynamic process
regulated by various pro-and anti-angiogenic molecules, which plays a crucial role in tumor …

[HTML][HTML] Molecular bases of VEGFR-2-mediated physiological function and pathological role

X Wang, AM Bove, G Simone, B Ma - Frontiers in Cell and …, 2020 - frontiersin.org
The vascular endothelial growth factors (VEGFs) and their receptors (VEGFRs) play crucial
roles in vasculogenesis and angiogenesis. Angiogenesis is an important mechanism in …

[HTML][HTML] Inflammation-mediated angiogenesis in ischemic stroke

H Zhu, Y Zhang, Y Zhong, Y Ye, X Hu, L Gu… - Frontiers in Cellular …, 2021 - frontiersin.org
Stroke is the leading cause of disability and mortality in the world, but the pathogenesis of
ischemic stroke (IS) is not completely clear and treatments are limited. Mounting evidence …

Design, synthesis, and anti-proliferative evaluation of new quinazolin-4 (3H)-ones as potential VEGFR-2 inhibitors

K El-Adl, AGA El-Helby, RR Ayyad, HA Mahdy… - Bioorganic & Medicinal …, 2021 - Elsevier
Inhibiting VEGFR-2 has been set up as a therapeutic strategy for treatment of cancer. Thus,
nineteen new quinazoline-4 (3H)-one derivatives were designed and synthesized …

[HTML][HTML] Modified benzoxazole-based VEGFR-2 inhibitors and apoptosis inducers: design, synthesis, and anti-proliferative evaluation

A Elwan, AE Abdallah, HA Mahdy, MA Dahab… - Molecules, 2022 - mdpi.com
This work is one of our efforts to discover potent anticancer agents. We modified the most
promising derivative of our previous work concerned with the development of VEGFR-2 …

Phthalazine‐based VEGFR‐2 inhibitors: Rationale, design, synthesis, in silico, ADMET profile, docking, and anticancer evaluations

F Khedr, MK Ibrahim, IH Eissa… - Archiv der …, 2021 - Wiley Online Library
In the designed compounds, a new linker was inserted in the form of fragments with verified
VEGFR‐2 inhibitory potential, including an α, β‐unsaturated ketonic fragment, pyrazole, and …

[HTML][HTML] miR-539 activates the SAPK/JNK signaling pathway to promote ferropotosis in colorectal cancer by directly targeting TIPE

Y Yang, Z Lin, Z Han, Z Wu, J Hua, R Zhong… - Cell Death …, 2021 - nature.com
Colorectal cancer (CRC) is a common tumor that harms human health with a high
recurrence rate. It has been reported that the expression of microRNA-539 (miR-539) is low …

[HTML][HTML] Mechanism and application of ferroptosis in colorectal cancer

L Yang, Y Zhang, Y Zhang, Z Fan - Biomedicine & Pharmacotherapy, 2023 - Elsevier
Colorectal cancer (CRC) is the third most common malignant tumor in the world. CRC has
high morbidity and mortality rates and it is a serious threat to human health. Ferroptosis is a …

Design, synthesis, docking, ADMET profile, and anticancer evaluations of novel thiazolidine‐2, 4‐dione derivatives as VEGFR‐2 inhibitors

K El‐Adl, H Sakr, SSA El‐Hddad… - Archiv der …, 2021 - Wiley Online Library
The anticancer activity of novel thiazolidine‐2, 4‐diones was evaluated against HepG2, HCT‐
116, and MCF‐7 cells. Among the tested cancer cell lines, HCT‐116 was the most sensitive …

[HTML][HTML] FAK regulates VEGFR2 expression and promotes angiogenesis in triple-negative breast cancer

JP Shiau, CC Wu, SJ Chang, MR Pan, W Liu… - Biomedicines, 2021 - mdpi.com
Triple-negative breast cancer (TNBC) remains a significant clinical challenge because of its
high vascularity and metastatic and recurrent rates. Tumor angiogenesis is considered an …