Deciphering the Anticancer Arsenal of Piper longum: Network Pharmacology and Molecular Docking Unveil Phytochemical Targets Against Lung Cancer

被引:1
作者
Varadharajan, Venkatramanan [1 ]
Balu, Ashwath Kumar [1 ]
Shiju, Atul [1 ]
Muthuramalingam, Pandiyan [2 ]
Shin, Hyunsuk [2 ]
Venkidasamy, Baskar [3 ]
Alharbi, Naiyf S. [4 ]
Kadaikunnan, Shine [4 ]
Thiruvengadam, Muthu [5 ]
机构
[1] PSG Coll Technol, Dept Biotechnol, Coimbatore, India
[2] Gyeongsang Natl Univ, Coll Agr & Life Sci, Div Hort Sci, Jinju 52725, South Korea
[3] Saveetha Univ, Dept Oral & Maxillofacial Surg, Saveetha Dent Coll & Hosp, Saveetha Inst Med & Tech Sci SIMATS, Chennai 600077, India
[4] King Saud Univ, Coll Sci, Dept Bot & Microbiol, POB 2455, Riyadh 11451, Saudi Arabia
[5] Konkuk Univ, Coll Sanghuh Life Sci, Dept Crop Sci, Seoul, South Korea
来源
INTERNATIONAL JOURNAL OF MEDICAL SCIENCES | 2024年 / 21卷 / 10期
关键词
Computational screening; Drug discovery; Medicinal plant compounds; Bioactivity; Oncogenes; PREDICTION; PATHWAY; CATENIN; GENES; CELLS;
D O I
10.7150/ijms.98393
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction: Lung cancer, characterized by uncontrolled cellular proliferation within the lung tissues, is the predominant cause of cancer-related fatalities worldwide. The traditional medicinal herb Piper longum has emerged as a significant contender in oncological research because of its documented anticancer attributes, suggesting its potential for novel therapeutic development. Methods: This study adopted network pharmacology and omics methodology to elucidate the anti-lung cancer potential of P. longum by identifying its bioactive constituents and their corresponding molecular targets. Results: Through a comprehensive literature review and the Integrated Medicinal Plant Phytochemistry and Therapeutics database (IMPPAT), we identified 33 bioactive molecules from P. longum. . Subsequent analyses employing tools such as SwissTargetPrediction, SuperPred, and DIGEP-Pred facilitated the isolation of 676 potential targets, among which 72 intersected with 666 lung cancer-associated genetic markers identified through databases including the Therapeutic Target Database (TTD), Online Mendelian Inheritance in Man (OMIM), and GeneCards. Further validation through protein-protein interaction (PPI) networks, gene ontology, pathway analyses, boxplots, and overall survival metrics underscored the therapeutic potential of compounds such as 7-epi-eudesm-4(15)-ene-1 beta, demethoxypiplartine, methyl 3,4,5-trimethoxycinnamate, 6-alpha-diol, and aristolodione. Notably, our findings reaffirm the relevance of lung cancer genes, such as CTNNB1, STAT3, HIF1A, HSP90AA1, and ERBB2, integral to various cellular processes and pivotal in cancer genesis and advancement. Molecular docking assessments revealed pronounced affinity between 6-alpha-diol and HIF1A, underscoring their potential as therapeutic agents for lung cancer. Conclusion: This study not only highlights the bioactive compounds of P. longum but also reinforces the molecular underpinnings of its anticancer mechanism, paving the way for future lung cancer therapeutics.
引用
收藏
页码:1915 / 1928
页数:14
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