Journals / Türk Biyokimya Dergisi / 2020 / Cilt: 45 - Sayı: 6

The effects of silibinin on oxidative stress and microRNA-10b expression in animal models of breast cancer

[Meme Kanseri Hayvan Modellerinde Silibininin Oksidatif Stres ve MicroRNA-10b Ekspresyonu Üzerine Etkileri]

Pages
707–714
Publication Date
2022-11-06
DOI
—
🏛️Bibliographic metadata and full text access for this article are provided via DergiPark.
DergiPark Record ↗
✨

AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

Data were analyzed using one-wayANOVA, Kruskal–Wallis, Mann–Whitney and t-test (p

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Background and aims: Among the factors associated withcancer are the oxidative stress and increased expression ofsome microRNA (miRs).
📊
Key Findings & Data:Silibinin has an anti-tumor effect.Therefore, this study evaluates the effects of silibinin onoxidative stress indices and miR-10b expression in theanimal models of breast cancer.Material and methods: In this study, 48 Balb/c mice weredivided into six groups (each group contains eight mice): thehealthy control, the cancer control, the healthy groupreceiving 20mg of silibinin, the cancer group receiving 20 mgof silibinin, the cancer group receiving 40mg of silibinin andthe cancer group receiving 80mg of silibinin for three weeks.In order to induce cancer, 4T1 cell line was used.
💡
Conclusion & Impact:Data were analyzed using one-wayANOVA, Kruskal–Wallis, Mann–Whitney and t-test (p
🔬Design:Modeling & Simulation
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Background and aims: Among the factors associated withcancer are the oxidative stress and increased expression ofsome microRNA (miRs). Silibinin has an anti-tumor effect.Therefore, this study evaluates the effects of silibinin onoxidative stress indices and miR-10b expression in theanimal models of breast cancer.Material and methods: In this study, 48 Balb/c mice weredivided into six groups (each group contains eight mice): thehealthy control, the cancer control, the healthy groupreceiving 20mg of silibinin, the cancer group receiving 20 mgof silibinin, the cancer group receiving 40mg of silibinin andthe cancer group receiving 80mg of silibinin for three weeks.In order to induce cancer, 4T1 cell line was used. Afterobtaining breast tumor samples, the levels of Malondialdehyde(MDA), superoxide dismutase (SOD), glutathioneperoxidase (GPX) and miR-10b expression in breast tumorbiopsy were evaluated. Data were analyzed using one-wayANOVA, Kruskal–Wallis, Mann–Whitney and t-test (p

Özet

Giriş ve Amaç: Oksidatif stres ve bazı artmış microRNA (miR’lerin) ekspresyonu kanserle ilişkili faktörler arasındadır. Silibininin bir anti-tümör etkisi vardır. Bu nedenle bu çalışmanın amacı, meme kanserinin hayvan modellerinde silibininin oksidatif stres indeksleri ve miR-10b ekspresyonu üzerindeki etkilerini değerlendirmektedir. Gereç ve Yöntemler: Bu çalışmada 48 Balb / c fare 6 gruba ayrıldı (her grup 8 fare içerir): sağlıklı kontrol, kanser kontrolü, 20 mg silibinin alan sağlıklı grup, 20 mg alan kanser grubu 40mg silibinin alan kanser grubu ve 3 hafta boyunca 80 mg silibinin alan kanser grubu. Kanseri indüklemek için 4T1 hücre hattı kullanıldı. Meme tümör örnekleri elde edildikten sonra, göğüs tümör biyopsisinde Malondialdehid (MDA), süperoksit dismutaz (SOD), glutatyon peroksidaz (GPX) ve miR-10b ekspresyon seviyeleri değerlendirildi. Veriler tek yönlü ANOVA, Kruskal–Wallis, Mann–Whitney ve T testi kullanılarak analiz edildi (p

🔖

Cite This Article

SOLEİMANİ, F., SHARİFİ, R., MAHMOODİ, M., KASSAEE, S. M. (2022). The effects of silibinin on oxidative stress and microRNA-10b expression in animal models of breast cancer. Türk Biyokimya Dergisi, Cilt: 45 - Sayı: 6, 707–714. https://ajindex.com/articles/620760

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (14)

  1. Nafissi N, Khayamzadeh M, Zeinali Z, Pazooki D, Hosseini M, Akbari ME. Epidemiology and histopathology of breast cancer in Iran vs. other Middle Eastern countries. Middle East J Cancer 2015; 6:243–51
  2. Nourazarian AR, Kangari P, Salmaninejad A. Roles of oxidative stress in the development and progression of breast cancer. Asian Pac J Cancer Prev 2014;15:4745–51
  3. Sharifi R, Nouri M, Eidi A, Noormohammadi Z, Dolatkhah H, Shirmohammadi M. Dietary PUFA increase apoptosis in stomach of patients with dyspeptic symptoms and infected with H. pylori. Lipids 2017;52:549–58
  4. Bjelakovic G, Nikolova D, Gluud C. Antioxidant supplements and mortality. Curr Opin Clin Nutr Metab Care 2014;17:40–4
  5. Wang Y, Branicky R, Noë A, Hekimi S. Superoxide dismutases: dual roles in controlling ROS damage and regulating ROS signaling. J Cell Biol 2018 Jun 4;217:1915–28
  6. Tan BL, Norhaizan ME, Liew W-P-P, Sulaiman Rahman H. Antioxidant and oxidative stress: a mutual interplay in agerelated diseases. Front Pharmacol 2018;9:1–28
  7. Rao S, Kumari S. Changes in plasma lipid peroxidation and the antioxidant system in women with breast cancer. IJBAS 2012;1: 429–38
  8. Zhang Y, Chan HF, Leong KW. Advanced materials and processing for drug delivery: the past and the future. Adv Drug Deliv Rev 2013;65:104–20
  9. Sheedy P, Medarova Z. The fundamental role of miR-10b in metastatic cancer. Am J Cancer Res 2018;8:1674–88. PMID: 30323962
  10. Zadeh MM, Motamed N, Ranji N, Majidi M, Falahi F. Silibinininduced apoptosis and downregulation of microRNA-21 and microRNA-155 in MCF-7 human breast cancer cells. J Breast Cancer 2016;19:45–52
  11. Pashaei-Asl F, Pashaei-Asl R, Khodadadi K, Akbarzadeh A, Ebrahimie E, Pashaiasl M. Enhancement of anticancer activity by silibinin and paclitaxel combination on the ovarian cancer. Artif Cells Nanomed Biotechnol 2018 Nov;46:1483–7
  12. Loguercio C, Festi D. Silybin and the liver: from basic research to clinical practice. World J Gastroenterol 2011;17:2288–301
  13. Soleimani N, Farhangi B, Mohabati MA, Etyabi F. VEGF and MMP-9 gene expression caused by treatment with helicobacter pylori neutrophilactivating recombinant protein in a breast cancer model. JBUMS 2015;17:13–9 (persian)
  14. Khan AQ, Khan R, Tahir M, Rehman MU, Lateef A, Ali F, et al. Silibinin inhibits tumor promotional triggers and tumorigenesis against chemically induced two-stage skin carcinogenesis in Swiss albino mice: possible role of oxidative stress and inflammation. Nutr Canc 66 2