Efecto del extracto de semillas de Brassica nigra contra la proliferación hepatocelular inducida por fenobarbital como agente promotor de tumors

Autores/as

  • Ibtehal Naseer Salman
  • Bahir Abdul Razzaq Mshimesh
  • Dalya Basil Hanna
  • Ghaith Ali Jasim

Palabras clave:

Proliferación hepatocelular, Fenobarbital, Semillas de Brassica.

Resumen

La proliferación hepatocelular es una de las principales causas de carcinoma hepatocelular (HCC) y es un tipo de muerte relacionada con el cáncer ampliamente distribuido. Existen desafíos considerables en el tratamiento del carcinoma hepatocelular, incluida la ineficacia, los efectos adversos y la resistencia a los medicamentos disponibles. Se ha establecido que un alto consumo de vegetales Brassica está relacionado con un menor riesgo de muchos tipos de cáncer. En el estudio se extrajeron semillas de Brassica nigra; Se realizó un análisis fitoquímico del extracto, incluidas pruebas de selección fitoquímica y análisis de cromatografía de gases-espectrometría de masas (GC-MS). La actividad antiproliferativa del extracto hidroalcohólico de semillas de Brassica se estudió a 800 mg/kg y se comparó con el grupo de control (administrado con solución salina normal), el grupo de fenobarbital (fenobarbital 75 mg/kg) y el grupo combinado (extracto de Brassica 800 mg/kg + fenobarbital 75 mg/kg). El análisis GC-MS reveló la presencia del compuesto de isotiocianato. En comparación con el grupo de fenobarbital, la combinación de grupos pretratados con semillas de Brassica nigra durante 14 días y fenobarbital durante siete días provocó una reducción significativa en la expresión de Ki67 y Bcl2 que fue evidente en los portaobjetos inmunohistoquímicos. Además, los grupos de combinación mostraron una disminución sustancial en el nivel de expresión de genes relacionados con el ciclo celular, incluidos los genes de mantenimiento de minicromosomas 2 (Mcm2) y ciclina A2 (Ccna2), y una reducción significativa en el nivel de expresión de Citocromo P450, incluidos CYP2B10 y CYP2C29 en comparación con el grupo fenobarbital. El extracto de semillas de Brassica nigra mostró efectos antiproliferativos y apoptóticos en el tejido hepático, lo que sugiere que tiene un impacto beneficioso para minimizar el riesgo de cáncer de hígado.

Descargas

Los datos de descargas todavía no están disponibles.

Citas

Issues CC. Current Clinical Issues Liver Cancer on the Rise TO. 2005;1029–32.‏

Yoon SK. Molecular mechanism of hepatocellular carcinoma. Hepatoma Res. 2018;4(8):42.

Bialecki ES, Di Bisceglie AM. Diagnosis of hepatocellular carcinoma. Hpb. 2005;7(1):26–34.

Sukowati CHC, Rosso N, Crocè LS, Tiribelli C. Hepatic cancer stem cells and drug resistance: Relevance in targeted therapies for hepatocellular carcinoma. World J Hepatol. 2010;2(3):114–26.

Llovet JM, Kelley RK, Villanueva A, Singal AG, Pikarsky E, Roayaie S, et al. Hepatocellular carcinoma. Nat Rev Dis Prim [Internet]. 2021;7(1). Available from: http://dx.doi.org/10.1038/s41572-020-00240-3

de Rosamel L, Blanc JF. Emerging tyrosine kinase inhibitors for the treatment of hepatocellular carcinoma. Expert Opin Emerg Drugs [Internet]. 2017;22(2):175–90. Available from: https://doi.org/10.1080/14728214.2017.1336538

Wege H, Li J, Ittrich H. Treatment Lines in Hepatocellular Carcinoma. Visc Med. 2019;35(4):266–72.

London SJ, Yuan JM, Chung FL, Gao YT, Coetzee GA, Ross RK, et al. Isothiocyanates, glutathione S-transferase M1 and T1 polymorphisms, and lung-cancer risk: A prospective study of men in Shanghai, China. Lancet. 2000;356(9231):724–9.

Smith TK, Lund EK, Clarke RG, Bennett RN, Johnson IT. Effects of Brussels sprout juice on the cell cycle and adhesion of human colorectal carcinoma cells (HT29) in vitro. J Agric Food Chem. 2005;53(10):3895–901.

Van Poppel G, Verhoeven DTH, Verhagen H, Goldbohm RA. Brassica vegetables and cancer prevention: Epidemiology and mechanisms. Adv Exp Med Biol. 2000;472:159–68.

Giovannucci E, Rimm EB, Liu Y, Stampfer MJ, Willett WC. A Prospective Study of Cruciferous Vegetables and Prostate Cancer. Cancer Epidemiol Biomarkers Prev. 2003;12(12):1403–9.

Abbaoui B, Lucas CR, Riedl KM, Clinton SK, Mortazavi A. Cruciferous Vegetables, Isothiocyanates, and Bladder Cancer Prevention. Mol Nutr Food Res. 2018;62(18):1–14.

Zhao H, Lin J, Grossman HB, Hernandez LM, Dinney CP, Wu X. Dietary isothiocyanates, GSTM1, GSTT1, NAT2 polymorphisms and bladder cancer risk. Int J Cancer. 2007;120(10):2208–13.

Mastuo T, Miyata Y, Yuno T, Mukae Y, Otsubo A, Mitsunari K, et al. Molecular mechanisms of the anti-cancer effects of isothiocyanates from cruciferous vegetables in bladder cancer. Molecules. 2020;25(3).

Omoja V, Ihedioha T, Eke G, PeterAjuzie I, Okezie S. Evaluation of the acute toxicity, phytochemical constituents and anti - ulcer properties of methanolic leaf extract of Annona muricata in mice. J Intercult Ethnopharmacol. 2014;3(1):37.

Evans W.C. Trease and Evan's Pharmacognosy. Haroourt Publishers,London, ISBN: 0702026174, 336-337.

Harborne J.B. Phytochemicsal methods: A Guide to Modern Techniques of Plant Analysis. London, Chapman and Hall, 2007; ISBN: 81-8128-410-4, 1-34.

Khalaf HA, Mahdi MF, and Abaas IS. Preliminary Phytochemical and GC-MS analysis of chemical constituents of Iraqi Plantago lanceoleta L. Al-Mustansiriyah Journal of Pharmaceutical Sciences (AJPS) (2018); 18.2: 114-121‏.‏

Anthony L. Junqueira’s Basic Histology text and atlas. Edition. McGraw-Hill Education. 2016

Alaa HO, Mshimesh BA, Mohsin RA. Studying the Toxicity of Hydroalcoholic Caraway Seeds Extract in Female Rats.Al-Mustansiriyah Journal of Pharmaceutical Sciences (AJPS) (2020); 20.2: 46-54.‏

Alzwaini A, Abbas WA, Alzubbaidi SH, Aljaleeli AN, Almugdadi SF. Vascular Endothelial Growth Factor (VEGF-C) Protein Expression Related with Lymphangiogensis in Iraqi Cervical Cancer Patients. Al-Mustansiriyah Journal of Pharmaceutical Sciences (AJPS) (2019); 19.4: 28-40.‏

Elabscience.Immunohistochemistry kit protocol.Aavailable from: techsupport@elabscience.comtechsupport@elabscience.com, other: www.elabscience.comwww.elabscience.com

Al-Ghamdi TH, Shafek Atta I. Efficacy of interleukin-6 in the induction of liver cell proliferation after hemi-hepatectomy: histopathologic and immunohistochemical study. Int J Clin Exp Pathol [Internet]. 2020;13(7):1540–9. Available from: www.ijcep.com/

Krajewska M, Krajewski S, Epstein JI, Shabaik A, Sauvageot J, Song K, et al. Immunohistochemical analysis of bcl-2, bax, bcl-X, and mcl-1 expression in prostate cancers. Am J Pathol. 1996;148(5):1567–76.

Trans,RNA extraction protocol, Available from: www.transgenbiotech.com, other info@ transgenbiotech.com

Trans,Transcript one step gDNA removal and cDNA synthesis protocol, Available from: www.transgenbiotech.com, other info@ transgenbiotech.com

Trans,qPCR protocol, Available from: www.transgenbiotech.com, other info@ transgenbiotech.com

Livak K, Piña A. Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT Method Related papers Analysis of Relat ive Gene Expression Dat a Using Real-T ime Quant it at ive PCR and t he 2 C T M…. Methods [Internet]. 2001;25(4):402–8. Available from: www.idealibrary.com

Balogh J, Iii DV, Gordon S, Li X, Ghobrial RM, Jr HPM. Jhc-3-041. J Hepatocell Carcinoma [Internet]. 2016; Volume 3:41–53. Available from: https://www.dovepress.com/hepatocellular-carcinoma-a-review-peer-reviewed-article-JHC.

Kim E, Viatour P. Hepatocellular carcinoma: old friends and new tricks. Exp Mol Med [Internet]. 2020;52(12):1898–907. Available from: http://dx.doi.org/10.1038/s12276-020-00527-1.‏

Mishra V, Mishra M, Chaudhari BP, Khanna R, Das M. Argemone Oil and Butter Yellow Induced Toxicity in Hepatic and Extra Hepatic Tissues. Bioenergetics 3: 111. doi: 10.4172/2167-7662.1000111 Page 2 of 7 Volume 3• Issue 1• 1000111 Bioenergetics ISSN: 2167-7662 BEG an open access journal adenine dinucleotide phosphate reduced (NADPH), bovine serum albumin (BSA) were purchased from Sigma Chemical Company, St. Louis, MO, USA. Argemone mexicana. 2014.

Verhoeven DTH, Goldbohm RA, Van Poppel G, Verhagen H, Van Den Brandt PA. Epidemiological studies on Brassica vegetables and cancer risk. Cancer Epidemiol Biomarkers Prev. 1996;5(9):733–48.

Kristal AR. Brassica vegetables and prostate cancer risk: A review of the epidemiologic evidence. Pharm Biol. 2002; 40(SUPPL.):55–8.

Nandini T, Ramya Sree D, Janbee S, Siva Sai Kiran K, Raveendra Babu G. Study of immunomodulatory effect of seeds of Brassica nigra and Cuminum cyminum in albino rats. Int J Pharm Clin Res. 2016;8(1):10–4.

Kinghorn AD, Ren Y, Li J, Sung CK. Cancer chemopreventive activity of higher plants. Plant Bioactives and Drug Discovery: Principles, Practice, and Perspectives. 2012 Apr 6:337-57.

Upwar N, Patel R, Waseem N, Mahobia N. In vitro anthelmintic activity of Brassica nigra Linn. seeds. (2011).

Anand P, Murali YK, Tandon V, Murthy PS, Chandra R. Insulinotropic effect of aqueous extract of Brassica nigra improves glucose homeostasis in streptozotocin induced diabetic rats. Exp Clin Endocrinol Diabetes. 2009;117(6):251–6.‏

Basha SN, Rekha R, Saleh S, Yemane S. Evaluation of invitro anthelmintic activities of Brassica nigra, Ocimum basilicum and Rumex abyssinicus. Pharmacogn J. 2011;3(20):88–92.

Radha Krishnan K, Azhagu Saravana Babu P, Babuskin S, Sivarajan M, Sukumar M. Modeling the Kinetics of Antioxidant Extraction from Origanum vulgare and Brassica nigra. Chem Eng Commun. 2015;202(12):1577–85.

Uddin MS, Millat MS, Islam MS, Hussain MS, Uddin MG, Siddiqui SA, et al. Exploration of in vitro thrombolytic, anthelminthic, cytotoxic and in vivo anxiolytic potentials with phytochemical screening of flowers of Brassica nigra. Futur J Pharm Sci. 2020;6(1).

Danlami U. Phytochemical, Nutritional and Antimicrobial Evaluations of the Aqueous Extract of Brassica Nigra (Brassicaceae) Seeds. 2016; 4(4):161.

Basha SN, Rekha R, Saleh S, Yemane S. Evaluation of invitro anthelmintic activities of Brassica nigra, Ocimum basilicum and Rumex abyssinicus. Pharmacogn J. 2011;3(20):88–92.

Sharma A, Rai PK, Prasad S. GC–MS detection and determination of major volatile compounds in Brassica juncea L. leaves and seeds. Microchem J [Internet]. 2018;138(2017):488–93. Available from: https://doi.org/10.1016/j.microc.2018.01.015

Shizu R, Benoki S, Numakura Y, Kodama S, Miyata M, Yamazoe Y, et al. Xenobiotic-Induced Hepatocyte Proliferation Associated with Constitutive Active/Androstane Receptor (CAR) or Peroxisome Proliferator-Activated Receptor α (PPARα) Is Enhanced by Pregnane X Receptor (PXR) Activation in Mice. PLoS One. 2013;8(4).

Dzulkifli FA, Mashor MY, Jaafar H. An overview of recent counting methods for Ki67 IHC staining. J Biomed Clin Sci. 2018;3(2):10–7.

Vrca I, Šćurla J, Kević N, Burčul F, Čulić FC, Bočina I, Blažević I, et al. Influence of isolation techniques on the composition of glucosinolate breakdown products, their antiproliferative activity and gastrointestinal stability of allyl isothiocyanate. Eur Food Res Technol (2022); 248, 567–576. https://doi.org/10.1007/s00217-021-03903-x

Sanders S, Thorgeirsson SS. Phenobarbital promotes liver growth in c-myc/TGF-α transgenic mice by inducing hypertrophy and inhibiting apoptosis. Carcinogenesis. 1999;20(1):41–9.

de Felippe Junior F. Isothiocyanates in cancer – Sulforaphane and their relatives. 2007;520–30

Jie M, Cheung WM, Yu V, Zhou Y, Tong PH, Ho JWS. Anti-proliferative activities of sinigrin on carcinogen-induced hepatotoxicity in rats. PLoS One. 2014;9(10):1–9.

Ahmed AG, Hussein UK, Ahmed AE, Kim KM, Mahmoud HM, Hammouda O, et al. Mustard Seed (Brassica nigra) Extract Exhibits Antiproliferative Effect against Human Lung Cancer Cells through Differential Regulation of Apoptosis, Cell Cycle, Migration, and Invasion. Molecules [Internet] 2020;25(9):2069. Available from: http://dx.doi.org/10.3390/molecules25092069

Tripathi K, Hussein UK, Anupalli R, Barnett R, Bachaboina L, Scalici J, et al. Allyl isothiocyanate induces replication-associated DNA damage response in NSCLC cells and sensitizes to ionizing radiation. Oncotarget. 2015;6(7):5237–52.

Zhang Y. Allyl isothiocyanate as a cancer chemopreventive phytochemical. Mol Nutr Food Res. 2010;54(1):127–35.‏

Li L, Bao X, Zhang QY, Negishi M, Ding X. Role of Cyp2b in phenobarbital-induced hepatocyte proliferation in mice. Drug Metab Dispos. 2017;45(8):977–81.

Cartea ME, Velasco P. Glucosinolates in Brassica foods: Bioavailability in food and significance for human health. Phytochem Rev. 2008;7(2):213–29.

Dusek J, Skoda J, Holas O, Horvatova A, Smutny T, Linhartova L, et al. Stilbene compound trans-3,4,5,4´-tetramethoxystilbene, a potential anticancer drug, regulates constitutive androstane receptor (Car) target genes, but does not possess proliferative activity in mouse liver. Toxicol Lett [Internet]. 2019;313(March):1–10. Available from: https://doi.org/10.1016/j.toxlet.2019.05.024

Qing Y, Debbie D, Laurence S. Characterization of mouse small intestinal cytochrome P450 expression. Drug Metabolism and Disposition November 2003, 31(11)1346-1351; DOI: https://doi.org/10.1124/dmd.31.11.1346

Hecht SS. Inhibition of carcinogenesis by isothiocyanates. Drug Metab Rev. 2000;32(3–4):395–411.

Fahey JW, Haristoy X, Dolan PM, Kensler TW, Scholtus I, Stephenson KK, et al. and antibiotic-resistant strains of Helicobacter pylori and prevents benzo [a] pyrene- induced stomach tumors. Pnas. 2002;7610–5.

Anilakumar K, Farhath K, Amarinder. Dietary role of glucosinolate derivatives: a review. Journal of Food Science and Technology-Mysore 43.1 (2006):8-17.‏

Nori W, Roomi AB, Akram W. Platelet indices as predictors of fetal growth restriction in Pre-eclamptic Women. Revista Latinoamericana de Hipertensión. 2020;15(4):280-5.

Vargas MÁ, Rosas ME. Impacto de un programa de actividad física aeróbica en adultos mayores con hipertensión arterial. Revista Latinoamericana de hipertensión. 2019;14(2):142-9.

Gualaquiza González R, Pérez Granja A, Tapia Caisaguano A, Legña Tibanta D, Bastidas Jiménez E, Gaibor Ortiz A, Bastidas Haro T, Allauca Yumiseba M, Bravo Bohórquez G, Miranda Buenaño F, Castañeda Morales D. Incidencia y características clínicas de lactantes menores con neumonía adquirida en la comunidadingresados en el Hospital Pediátrico “Baca Ortiz”, Ecuador. Archivos venezolanos de farmacología y terapéutica. 2020;39(4):260-3.

Descargas

Publicado

2023-04-05

Cómo citar

Naseer Salman, I., Razzaq Mshimesh, B. A., Basil Hanna, D. ., & Ali Jasim, G. . (2023). Efecto del extracto de semillas de Brassica nigra contra la proliferación hepatocelular inducida por fenobarbital como agente promotor de tumors . AVFT – Archivos Venezolanos De Farmacología Y Terapéutica, 41(7). Recuperado a partir de https://saber.ucv.ve/ojs/index.php/rev_aavft/article/view/25939