Network Pharmacology and Pathway Enrichment Analysis of Murraya koenigii Phytochemicals Reveals Multitarget Potential Against Breast Cancer

Murraya koenigii (curry leaf) is a medicinal plant traditionally used in South Asian medicine and known to contain bioactive carbazole alkaloids with reported anticancer potential. This study aimed to evaluate the molecular mechanisms and multi-target potential of five key phytochemicals from M. koenigii such as: Koenimbine, Koenidine, Mahanimbine, Murrayazoline, and O-methylmurrayamine A, in the context of breast cancer, using a network pharmacology and pathway enrichment approach. Target prediction was performed using SwissTargetPrediction, and breast cancer–associated genes were retrieved from the GeneCards database. Intersection analysis revealed 21 overlapping genes, including major oncogenic drivers such as EGFR, ERBB2, PIK3CA, AKT1, CDK2, and AR. These targets are known to play central roles in tumor cell proliferation, hormone receptor signaling, survival, and therapeutic resistance. Functional pathway enrichment using ShinyGO demonstrated that the overlapping genes were significantly enriched in key breast cancer–related pathways, including PI3K-Akt signaling, MAPK signaling, endocrine resistance, ErbB signaling, and cell cycle control. Network visualization in Cytoscape further revealed that the phytochemicals engage interconnected targets, supporting the hypothesis of a polypharmacological mechanism. Taken together, these findings suggest that M. koenigii phytochemicals possess the potential to modulate multiple hallmarks of breast cancer through simultaneous interaction with diverse but functionally convergent targets. The study provides a systems-level framework for understanding the therapeutic promise of M. koenigii and establishes a strong foundation for further experimental validation in breast cancer models, particularly those resistant to conventional monotherapies. Keywords: breast cancer, Murraya koenigii, network pharmacology, phytochemicals, target prediction.

Authors

Institutions

Publication Details

Journal
International Journal of Research and Review
Published
2025-06-17
DOI
https://doi.org/10.52403/ijrr.20250639
Primary Topic
Synthesis and biological activity
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Network Pharmacology and Pathway Enrichment Analysis of Murraya koenigii Phytochemicals Reveals Multitarget Potential Against Breast Cancer

Puspa Hening, Andini Kusuma Putri, Nurina Tahta Afwi Maulina
International Journal of Research and Review
Synthesis and biological activity
article

Network Pharmacology and Pathway Enrichment Analysis of Murraya koenigii Phytochemicals Reveals Multitarget Potential Against Breast Cancer

Puspa Hening, Andini Kusuma Putri, Nurina Tahta Afwi Maulina
article en

Abstract

Murraya koenigii (curry leaf) is a medicinal plant traditionally used in South Asian medicine and known to contain bioactive carbazole alkaloids with reported anticancer potential. This study aimed to evaluate the molecular mechanisms and multi-target potential of five key phytochemicals from M. koenigii such as: Koenimbine, Koenidine, Mahanimbine, Murrayazoline, and O-methylmurrayamine A, in the context of breast cancer, using a network pharmacology and pathway enrichment approach. Target prediction was performed using SwissTargetPrediction, and breast cancer–associated genes were retrieved from the GeneCards database. Intersection analysis revealed 21 overlapping genes, including major oncogenic drivers such as EGFR, ERBB2, PIK3CA, AKT1, CDK2, and AR. These targets are known to play central roles in tumor cell proliferation, hormone receptor signaling, survival, and therapeutic resistance. Functional pathway enrichment using ShinyGO demonstrated that the overlapping genes were significantly enriched in key breast cancer–related pathways, including PI3K-Akt signaling, MAPK signaling, endocrine resistance, ErbB signaling, and cell cycle control. Network visualization in Cytoscape further revealed that the phytochemicals engage interconnected targets, supporting the hypothesis of a polypharmacological mechanism. Taken together, these findings suggest that M. koenigii phytochemicals possess the potential to modulate multiple hallmarks of breast cancer through simultaneous interaction with diverse but functionally convergent targets. The study provides a systems-level framework for understanding the therapeutic promise of M. koenigii and establishes a strong foundation for further experimental validation in breast cancer models, particularly those resistant to conventional monotherapies. Keywords: breast cancer, Murraya koenigii, network pharmacology, phytochemicals, target prediction.

International Journal of Research and ReviewVol. 12(6)
Diponegoro University (ID)
Good health and well-being
Openalex Percentile: Top 89%
Synthesis and biological activity
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.