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Unveiling the multifaceted antiproliferative efficacy of Cichorium endivia root extract by dual modulation of apoptotic and inflammatory genes, inducing cell cycle arrest, and targeting COX-2.
Alzahrani, Abdullah R; Hosny, Nora; Mohamed, Doaa I; Abo Nahas, Hebatallah H; Albogami, Abdulaziz; Al-Hazani, Tahani Mohamed Ibrahim; Ibrahim, Ibrahim Abdel Aziz; Falemban, Alaa Hisham; Bamagous, Ghazi A; Saied, Essa M.
Afiliação
  • Alzahrani AR; Department of Pharmacology and Toxicology, Faculty of Medicine, Umm Al-Qura University Makkah Saudi Arabia aralzahrani@uqu.edu.sa iamustafa@uqu.edu.sa ahfalemban@uqu.edu.sa gabamagous@uqu.edu.sa.
  • Hosny N; Medical Biochemistry and Molecular Biology Department, Faculty of Medicine, Suez Canal University Ismailia 41522 Egypt Ahmedn@umn.edu.
  • Mohamed DI; Center of Excellence in Molecular and Cellular Medicine, Faculty of Medicine, Suez Canal University Ismailia Egypt.
  • Abo Nahas HH; Department of Clinical Pharmacology and Therapeutics, Faculty of Medicine, Ain Shams University Cairo 11566 Egypt doaapharma@med.asu.edu.eg.
  • Albogami A; Zoology Department, Faculty of Science, Port Said University Port Said 42526 Egypt hebatallah_hassan@science.suez.edu.eg.
  • Al-Hazani TMI; Biology Department, Faculty of Science, Al-Baha University Al Aqiq Saudi Arabia aalbogami@bu.edu.sa.
  • Ibrahim IAA; Biology Department, College of Science and Humanities, Prince Sattam bin Abdulaziz University P. O. Box: 83 Al-Kharj 11940 Saudi Arabia t.alhazani@psau.edu.sa.
  • Falemban AH; Department of Pharmacology and Toxicology, Faculty of Medicine, Umm Al-Qura University Makkah Saudi Arabia aralzahrani@uqu.edu.sa iamustafa@uqu.edu.sa ahfalemban@uqu.edu.sa gabamagous@uqu.edu.sa.
  • Bamagous GA; Department of Pharmacology and Toxicology, Faculty of Medicine, Umm Al-Qura University Makkah Saudi Arabia aralzahrani@uqu.edu.sa iamustafa@uqu.edu.sa ahfalemban@uqu.edu.sa gabamagous@uqu.edu.sa.
  • Saied EM; Department of Pharmacology and Toxicology, Faculty of Medicine, Umm Al-Qura University Makkah Saudi Arabia aralzahrani@uqu.edu.sa iamustafa@uqu.edu.sa ahfalemban@uqu.edu.sa gabamagous@uqu.edu.sa.
RSC Adv ; 14(27): 19400-19427, 2024 Jun 12.
Article em En | MEDLINE | ID: mdl-38887636
ABSTRACT
Chicory (Cichorium endivia L. divaricatum) is a renowned medicinal plant traditionally used for various ailments, yet the pharmacological potential of its roots, particularly in terms of antitumor activity, remains elusive. In the present study, we explore, for the first time, the metabolomic profile of ethanolic extract from Cichorium endivia roots (CIR) and further unveil its antiproliferative potential. The untargeted phytochemical analysis UPLC/T-TOF-MS/MS identified 131 metabolites in the CIR extract, covering acids, amino acids, flavonoids, alkaloids, nucleotides, and carbohydrates. The antiproliferative activity of the CIR extract was tested in 14 cancer cell lines, revealing significant cytotoxicity (IC50 2.85-29.15 µg mL-1) and a high selectivity index. Among the cells examined, the CIR extract recorded the most potent antiproliferative activity and selectivity toward HepG2 and Panc-1 cells, with an IC50 of 2.85 µg mL-1 and 3.86 µg mL-1, respectively, and SI > 10. Insights into the mode of action of the antiproliferative activity revealed that CIR extract induces cell arrest in the S phase while diminishing cell distribution in the G0/G1 and G2/M phases in HepG-2 and Panc-1 cells. Flow cytometric and RT-PCR analysis revealed that the CIR extract significantly triggers apoptosis and modulates the expression of pro-apoptotic and anti-apoptotic genes. Furthermore, the CIR extract exhibited a pronounced anti-inflammatory activity, as evidenced by down-regulating key cytokines in LPS-induced RAW 264.7 cells and selectively inhibiting the COX-2 enzyme. Finally, the CIR extract showed a robust total antioxidant capacity, together with potent free radicals and metal scavenging properties, highlighting its role in alleviating oxidative stress. Taken together, this study highlights the multifaceted therapeutic potential of CIR extract as a natural-based antitumor supplement.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article