Cytotoxic Evaluation, Molecular Docking, Molecular Dynamics, and ADMET Prediction of Isolupalbigenin Isolated from Erythrina subumbrans (Hassk). Merr. (Fabaceae) Stem Bark: Unveiling Its Anticancer Efficacy.

IF 2.7 4区 医学 Q3 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
OncoTargets and therapy Pub Date : 2024-10-17 eCollection Date: 2024-01-01 DOI:10.2147/OTT.S482469
Tati Herlina, Abd Wahid Rizaldi Akili, Vicki Nishinarizki, Ari Hardianto, Allyn Pramudya Sulaeman, Shabarni Gaffar, Euis Julaeha, Tri Mayanti, Unang Supratman, Mohd Azlan Nafiah, Jalifah Binti Latip
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引用次数: 0

Abstract

Introduction: Erythrina subumbrans, a medical plant found in sub-Saharan Africa and the Western Ghats of India, shows promise as a potential source of bioactive compounds to treat cancer. In our ongoing research on folk medical plants, we report the isolation of flavonoid compound from the stem bark of E. subumbrans along with its cytotoxic activity against breast cancer (MCF-7 and T47D), and cervical cancer (HeLa) cell lines.

Purpose: This study aimed to isolate secondary metabolite from the stem bark of E. subumbrans and evaluate its cytotoxic activity to support the use of folk medicinal plants as alternative therapy against cancer.

Methods: Isolupalbigenin was isolated from the stem bark of E. subumbrans by column chromatography. Cytotoxic activity against breast cancer (MCF-7 and T47D) and cervical cancer (HeLa) cell lines was evaluated using the MTT assay, whereas the in silico study was evaluated using molecular docking and molecular dynamics against estrogen receptor alpha (ERα).

Results: The cytotoxic assay showed that isolupalbigenin inhibited the growth of MCF-7 cell with an IC50 of 31.62 µg∙mL-1, while showing no toxicity against normal human cells (Vero cell line). The molecular docking results suggested that isolupalbigenin can bind to ERα with a lower binding affinity than estradiol, whereas the stability of the isolupalbigenin-ERα complex was confirmed by molecular dynamic simulation with a median Root Mean Square Deviation (RMSD) of 2.80 Å. Toxicity prediction suggested that isolupalbigenin was less likely to cause hepatotoxicity or carcinogenicity, whereas pharmacokinetic prediction suggested that isolupalbigenin has high intestinal absorption with medium Caco2 permeability. In addition, isolupalbigenin was predicted to have a medium volume of distribution (Vd).

Conclusion: Isolupalbigenin isolated from the stem bark of E. subumbrans with cytotoxic activity supports further development of plants from the genus Erythrina as a medicinal plant for alternative therapy against cancer.

从 Erythrina subumbrans (Hassk).Merr.(豆科)茎皮中分离出的 Isolupalbigenin:揭示其抗癌功效。
简介Erythrina subumbrans 是一种生长在撒哈拉以南非洲和印度西高止山脉的药用植物,有望成为治疗癌症的生物活性化合物的潜在来源。在我们正在进行的有关民间药用植物的研究中,我们报告了从 E. subumbrans 茎皮中分离出的黄酮类化合物及其对乳腺癌(MCF-7 和 T47D)和宫颈癌(HeLa)细胞系的细胞毒性活性:方法:采用柱层析法从 E. subumbrans 的茎皮中分离出 Isolupalbigenin。方法:通过柱层析从 E subumbrans 的茎皮中分离出 Isolupalbigenin,并使用 MTT 法评估其对乳腺癌(MCF-7 和 T47D)和宫颈癌(HeLa)细胞系的细胞毒活性,同时使用分子对接和分子动力学方法评估其对雌激素受体α(ERα)的作用:细胞毒性试验表明,isolupalbigenin抑制MCF-7细胞生长的IC50为31.62 µg∙mL-1,而对正常人细胞(Vero细胞系)无毒性。分子对接结果表明,isolupalbigenin与ERα的结合亲和力低于雌二醇,而分子动力学模拟证实了isolupalbigenin-ERα复合物的稳定性,其中位数均方根偏差(RMSD)为2.80 Å。此外,预计isolupalbigenin的分布容积(Vd)适中:结论:从 E. subumbrans 茎皮中分离出的具有细胞毒性活性的 isolupalbigenin 支持将 Erythrina 属植物进一步开发为抗癌替代疗法的药用植物。
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来源期刊
OncoTargets and therapy
OncoTargets and therapy BIOTECHNOLOGY & APPLIED MICROBIOLOGY-ONCOLOGY
CiteScore
9.70
自引率
0.00%
发文量
221
审稿时长
1 months
期刊介绍: OncoTargets and Therapy is an international, peer-reviewed journal focusing on molecular aspects of cancer research, that is, the molecular diagnosis of and targeted molecular or precision therapy for all types of cancer. The journal is characterized by the rapid reporting of high-quality original research, basic science, reviews and evaluations, expert opinion and commentary that shed novel insight on a cancer or cancer subtype. Specific topics covered by the journal include: -Novel therapeutic targets and innovative agents -Novel therapeutic regimens for improved benefit and/or decreased side effects -Early stage clinical trials Further considerations when submitting to OncoTargets and Therapy: -Studies containing in vivo animal model data will be considered favorably. -Tissue microarray analyses will not be considered except in cases where they are supported by comprehensive biological studies involving multiple cell lines. -Biomarker association studies will be considered only when validated by comprehensive in vitro data and analysis of human tissue samples. -Studies utilizing publicly available data (e.g. GWAS/TCGA/GEO etc.) should add to the body of knowledge about a specific disease or relevant phenotype and must be validated using the authors’ own data through replication in an independent sample set and functional follow-up. -Bioinformatics studies must be validated using the authors’ own data through replication in an independent sample set and functional follow-up. -Single nucleotide polymorphism (SNP) studies will not be considered.
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