In silico assessment of coriander leaf extract active compound to resensitize oxaliplatin resistance in colorectal cancer mediated by ABCG2 and UPF1 proteins

Colorectal cancer is, and continues to be, one of the most important global health burdens due to its notorious high mortality rate and continuous resilience to traditional modes of treatment, specifically chemotherapeutic agents such as oxaliplatin. The resistance is mediated through specified genes highly involved in survival and resistant mechanisms in cancerous cells, like ABCG2 and UPF1 genes. Given the challenge, this study focuses on the coriander leaf extract as a new strategy for overcoming oxaliplatin resistance in colorectal cancer. In the present study, the authors examined the anticancer activities of the extracts from coriander leaves, which exerted inhibitory activity toward ABCG2 and UPF1 proteins believed to be involved in chemoresistance. Molecular docking analysis was done by PyRx software to evaluate the binding properties of the target genes with the 31 compounds in coriander leaf extract to find the best compound that may give an efficient way of overcoming resistance against oxaliplatin. Out of all the compounds screened, rutin came out to be the potential candidate. The binding affinities were highly impressive, about -8.4 kcal/mol for UPF1 and -7.8 kcal/mol for ABCG2. These values are especially important because they exceed the conventional affinity of known chemotherapy inhibitors, such as Ko143 and actinomycin D, which served as positive controls in this study. The higher binding affinity of rutin indicates that it may potentiate chemotherapy by specifically targeting ABCG2 and UPF1 in colorectal cancer cells. This strategic approach could limit the resistance to oxaliplatin and increase the treatment success rate in colorectal cancer patients. The observations of this work open up new perspectives in the study of natural products as adjuvants or alternatives to traditional chemotherapy that, in the future, could give rise to more efficient and less toxic strategies against colorectal cancer.

Authors

Institutions

Publication Details

Journal
Notulae Scientia Biologicae
Published
2024-12-18
DOI
https://doi.org/10.55779/nsb16412125
Primary Topic
Drug Transport and Resistance Mechanisms
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

In silico assessment of coriander leaf extract active compound to resensitize oxaliplatin resistance in colorectal cancer mediated by ABCG2 and UPF1 proteins

Arli Aditya Parikesit, Sánchez Gómez Jessica, Sandra B. FILEMON, Sharron SANTOSA et al.
Notulae Scientia Biologicae
Drug Transport and Resistance Mechanisms
article

In silico assessment of coriander leaf extract active compound to resensitize oxaliplatin resistance in colorectal cancer mediated by ABCG2 and UPF1 proteins

Arli Aditya Parikesit, Sánchez Gómez Jessica, Sandra B. FILEMON, Sharron SANTOSA, Stephani C. MAHARANI
article en

Abstract

Colorectal cancer is, and continues to be, one of the most important global health burdens due to its notorious high mortality rate and continuous resilience to traditional modes of treatment, specifically chemotherapeutic agents such as oxaliplatin. The resistance is mediated through specified genes highly involved in survival and resistant mechanisms in cancerous cells, like ABCG2 and UPF1 genes. Given the challenge, this study focuses on the coriander leaf extract as a new strategy for overcoming oxaliplatin resistance in colorectal cancer. In the present study, the authors examined the anticancer activities of the extracts from coriander leaves, which exerted inhibitory activity toward ABCG2 and UPF1 proteins believed to be involved in chemoresistance. Molecular docking analysis was done by PyRx software to evaluate the binding properties of the target genes with the 31 compounds in coriander leaf extract to find the best compound that may give an efficient way of overcoming resistance against oxaliplatin. Out of all the compounds screened, rutin came out to be the potential candidate. The binding affinities were highly impressive, about -8.4 kcal/mol for UPF1 and -7.8 kcal/mol for ABCG2. These values are especially important because they exceed the conventional affinity of known chemotherapy inhibitors, such as Ko143 and actinomycin D, which served as positive controls in this study. The higher binding affinity of rutin indicates that it may potentiate chemotherapy by specifically targeting ABCG2 and UPF1 in colorectal cancer cells. This strategic approach could limit the resistance to oxaliplatin and increase the treatment success rate in colorectal cancer patients. The observations of this work open up new perspectives in the study of natural products as adjuvants or alternatives to traditional chemotherapy that, in the future, could give rise to more efficient and less toxic strategies against colorectal cancer.

Notulae Scientia BiologicaeVol. 16(4)
Indonesia International Institute for Life Sciences (ID)
Good health and well-being
Openalex Percentile: Top 59%
Drug Transport and Resistance Mechanisms
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.