Evidence map›Paper›PMID 40552160›Full record

ArticleFrontiers in pharmacology2025

Structure-based molecular screening and dynamic simulation of phytocompounds targeting VEGFR-2: a novel therapeutic approach for papillary thyroid carcinoma.

Shuai Wang, Lingqian Zhang, Wenjun Zhang, Xiong Zeng, Jie Mei, Weidong Xiao, Lijie Yang

Abstract read
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Article in Frontiers in pharmacology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Shuai Wang *Department of General Surgery, Xinqiao Hospital, The Army Medical University, Chongqing, China.
Lingqian Zhang *Department of Hematology-Oncology, Chongqing University Cancer Hospital, Chongqing, China.
Wenjun ZhangDepartment of Hematology-Oncology, Chongqing University Cancer Hospital, Chongqing, China.
Xiong ZengDepartment of General Surgery, Xinqiao Hospital, The Army Medical University, Chongqing, China.
Jie MeiDepartment of General Surgery, Xinqiao Hospital, The Army Medical University, Chongqing, China.
Weidong XiaoDepartment of General Surgery, Xinqiao Hospital, The Army Medical University, Chongqing, China.
Lijie YangDepartment of General Surgery, Xinqiao Hospital, The Army Medical University, Chongqing, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Papillary thyroid carcinoma (PTC) is the most prevalent type of thyroid cancer, with aggressive variants presenting major therapeutic challenges. Vascular endothelial growth factor receptor-2 (VEGFR-2) is a key regulator of tumor angiogenesis and is highly expressed in PTC, making it a promising target for therapeutic intervention. This highlights the potential of VEGFR-2 inhibition as an effective strategy for managing PTC. In this study, we employed virtual drug screening, molecular dynamics simulations, and binding free energy calculations to identify potential VEGFR-2 inhibitors from the African natural product database (AfroDb). Our virtual drug screening identified three lead compounds SA_0090, 17.3.1.7.8 and BMC_0005 with a docking scores of -9.04 kcal/mol, -8.96 kcal/mol, and -8.33 kcal/mol respectively, surpassing the control compound (-8.39 kcal/mol). Molecular dynamics simulation analysis confirmed the dynamic stability, structural compactness, and minimal residual fluctuations of the 17.3.1.7.8 and BMC_0005 compounds-VEGFR2 complexes. The binding free energy calculations further supported the strong interactions, with values recorded as -60.3861 ± 0.39 kcal/mol for the control, -52.2732 ± 0.37 kcal/mol for SA_0090, -52.7797 ± 0.62 kcal/mol for 17.3.1.7.8, and -61.476 ± 0.59 kcal/mol for BMC_0005. Additionally, the selected compounds exhibited highly favorable ADMET properties, including optimal water solubility, efficient gastrointestinal absorption, and a non-hepatotoxic profile, all aligning with Lipinski's rule of five. In conclusion, these findings highlight 17.3.1.7.8 and BMC_0005 compounds as compelling candidates for VEGFR-2 inhibition, offering a promising therapeutic avenue for papillary thyroid carcinoma, warranting further

Indexed as

angiogenesismolecular dynamic simulationpapillary thyroid carcinomaVEGFR-2virtual drug screening

Identifiers

PMID40552160
PMCPMC12183223

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.