Green Seaweed Caulerpa racemosa as a Novel Non-Small Cell Lung Cancer Inhibitor in Overcoming Tyrosine Kinase Inhibitor Resistance: An Analysis Employing Network Pharmacology, Molecular Docking, and In Vitro Research

Lau, Vincent and Nurkolis, Fahrul and Park, Moon-nyeo and Heriyanto, Didik Setyo and Taslim, Nurpudji Astuti and Tallei, Trina Ekawati and Permatasari, Happy Kurnia and Tjandrawinata, Raymond R. and Moon, Seungjoon and Kim, Bonglee (2024) Green Seaweed Caulerpa racemosa as a Novel Non-Small Cell Lung Cancer Inhibitor in Overcoming Tyrosine Kinase Inhibitor Resistance: An Analysis Employing Network Pharmacology, Molecular Docking, and In Vitro Research. Marine Drugs, 22 (6). ISSN 16603397

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Abstract

The marine environment provides a rich source of distinct creatures containing potentially revolutionary bioactive chemicals. One of these organisms is Caulerpa racemosa, a type of green algae known as green seaweed, seagrapes, or green caviar. This organism stands out because it has great promise for use in medicine, especially in the study of cancer. Through the utilization of computational modeling (in silico) and cellular laboratory experiments (in vitro), the chemical components included in the green seaweed C. racemosa were effectively analyzed, uncovering its capability to treat non-small cell lung cancer (NSCLC). The study specifically emphasized blocking SRC, STAT3, PIK3CA, MAPK1, EGFR, and JAK1 using molecular docking and in vitro. These proteins play a crucial role in the EGFR Tyrosine Kinase Inhibitor Resistance pathway in NSCLC. The chemical Caulersin (C2) included in C. racemosa extract (CRE) has been identified as a potent and effective agent in fighting against non-small cell lung cancer (NSCLC), both in silico and in vitro. CRE and C2 showed a level of inhibition similar to that of osimertinib (positive control/NSCLC drug). © 2024 Elsevier B.V., All rights reserved.

Item Type: Article
Additional Information: Cited by: 10; All Open Access; Gold Open Access; Green Final Open Access; Green Open Access
Uncontrolled Keywords: ageratriol; antineoplastic agent; caulerpenyne; caulerpin; caulersin; epidermal growth factor receptor; hexadecanamide; icosapentaenoic acid; Janus kinase 1; mitogen activated protein kinase 1; natural product; oclacitinib; oleamide; osimertinib; phosphatidylinositol 4 phosphate kinase; protein tyrosine kinase inhibitor; racemosin; STAT3 protein; unclassified drug; acrylamide derivative; plant extract; protein kinase inhibitor; Article; Bryopsidales; Caulerpa racemosa; Caulerpaceae; computer model; controlled study; data base; drug analysis; EGFR signaling; estimated glomerular filtration rate; green alga; high performance liquid chromatography; human; human cell; in vitro study; molecular docking; non small cell lung cancer; nonhuman; seaweed; systems pharmacology; toxicity; Viridiplantae; Caulerpa; chemistry; drug effect; drug resistance; drug therapy; lung tumor; tumor cell line; Acrylamides; Antineoplastic Agents; Carcinoma, Non-Small-Cell Lung; Cell Line, Tumor; Drug Resistance, Neoplasm; ErbB Receptors; Humans; Lung Neoplasms; Molecular Docking Simulation; Network Pharmacology; Plant Extracts; Protein Kinase Inhibitors; Seaweed; Tyrosine Kinase Inhibitors
Subjects: R Medicine > RB Pathology
Divisions: Faculty of Medicine, Public Health and Nursing > Non Surgical Divisions
Depositing User: Ani PURWANDARI
Date Deposited: 08 Oct 2025 06:53
Last Modified: 08 Oct 2025 06:53
URI: https://ir.lib.ugm.ac.id/id/eprint/22358

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