Research Article
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Year 2021, Volume: 11 Issue: 1, 81 - 90, 31.03.2021
https://doi.org/10.33808/clinexphealthsci.787954

Abstract

Supporting Institution

Amasya Üniversitesi

Project Number

FMB-BAP 18-0333

References

  • [1] Jemal A, Siegel R, Ward E, Hao Y. Cancer Statistics, CA. Cancer J Clin. 2008;58(2):71-96.
  • [2] Siegel RL, Miller KD, Jemal A. Cancer Statistics, CA Cancer J Clin. 2017;67(1):7-30.
  • [3] World Health Organization. WHO. What is cancer?. https://www.who.int/cancer/en/ (2018).
  • [4] Saip P, Keskin S, Özkan M, Kaplan MA, Aydoğan F, Demirağ GG, et al. The Access Rate to Dıagnosıs and Treatment Modalıtıes in Breast Cancer Patıents in Turkey; Multıcenter Observatıonal Study. J. Breast Health. 2011;7:109-117.
  • [5] Jemal A, Siegel R, Ward E, Hao Y, Xu J, Thu MJ. Cancer statistics, CA. Cancer J Clin 2009; 59:225-249.
  • [6] Vaya J, Aviram M. Nutritional Antioxidants: Mechanisms of Action, Analyses of Activities and Medical Applications Curr. Med. Chem. – Imm., Endoc. & Metab. Agents, 2001;1:99-117.
  • [7] Valadez-Vega C, Delgado-Olivares L, Morales González JA, Alanís García E, Villagomez Ibarra JR, Ramírez Moreno, E., et al. The role of natural antioxidants in cancer disease. En Morales-González JA.(Edi.), Oxidative Stress and Chronic Degenerative Diseases - a Role for Antioxidants. 2013;391-418.
  • [8] Ganapathy V. Protein digestion and absorption. In Physiology of the Gastrointestinal Tract (Fifth Edition), Chapter 59 - Protein Digestion and Absorption, 2012;1595-1623.
  • [9] Cheng SB, Liu HT, Chen SY, Lin PT, Lai CY.Huang, YC. Changes of oxidative stress, glutathione, and its dependent antioxidant enzyme activities in patients with hepatocellular carcinoma before and after tumor resection. PloS one, 2017;12(1):e0170016.
  • [10] Deters M, Siegers CP, Strubelt O. Influence of glycine on the damage induced in isolated perfused rat liver by five hepatotoxic agents. Toxicology, 1998;128:63–72.
  • [11] Vaillancourt VA, Larsen SD, Tanis SP, Burr JE, Connell MA, Cudahy, MM. et al. Synthesis and biological activity of aminoguanidine and diaminoguanidine analogues of the antidiabetic/antiobesity agent 3-guanidinopropionic acid. J. Med. Chem., 2001;44(8):1231-1248.
  • [12] Bruns H, Kazanavicius D, Schultze D, Saeedi MA. Yamanaka K, Strupas K, et al. Glycine inhibits angiogenesis in colorectal cancer: Role of endothelial cells. Amino Acids, 2016;48: 2549-2558.
  • [13] Mukwevho E, Ferreira Z, Ayeleso A. Potential Role of Sulfur-Containing Antioxidant Systems in Highly Oxidative Environments. Molecules, 2014;19:19376-19389.
  • [14] Santhilkumar R, Sengottuvelan M, Nalini N. Protective effect of glycine supplementation in the levels of lipid peroxidation, and antioxidant enzymes in the erythrocyte of rats with alcohol-induced liver injury. Cell Biochem. Funct. 2004;22:123–128.
  • [15] Lim E, Hong D, Park J, Joung Y, Darvin P, Kim S, et al. Methylsulfonylmethane Suppresses Breast Cancer Growth by Down-Regulating STAT3 and STAT5b Pathways, PloS one, 2012;7(4): e33361.
  • [16] Kong CS, Bak SS, Rhee SH, Rho CW, Kim NK. Fermentation properties of young radish Kimchi prepared using young radish cultivated in the soil containing sulfur and it's inhibitory effect on the growth of AGS human gastric adenocarcinoma cells. J Korean Soc Food Sci Nutr., 2006;35:158–163.
  • [17] Ha AW, Hong KH, Kim HS, Kim WK. Inorganic sulfur reduces cell proliferation by inhibiting of ErbB2 and ErbB3 protein and mRNA expression in MDA-MB-231 human breast cancer cells. Nutrit. Res. Pract., 2013;7(2):89–95.
  • [18] Georgiou D, Toutountzoglou V, Muir KW, Hadjipavlou-Litina D, Elemes Y. Synthesis of sulfur containing dihydro-pyrrolo derivatives and their biological evaluation as antioxidants. Bio. Med. Chem., 2012;20(17):5103-5109.
  • [19] Pelit E, Oikonomou K, Gul M, Georgiou D, Szafert S, Katsamakas S, Elemes Y. α-Amination and the 5-exo-trig cyclization reaction of sulfur-containing Schiff bases with N-phenyltriazolinedione and their anti-lipid peroxidation activity. Com. Ren. Chim., 2017;20(4):424-434.
  • [20] Hoppe D, Beckmann L. Metallierte Stickstoff‐Derivate der Kohlensäure in der organischen Synthese, XIII. Selektive Mono‐ und Dialkylierung von N‐[Bis(alkylthio)‐methylen]glycin‐ethylestern zum Aufbau von kettenverlängerten und α‐verzweigten α‐Aminosäureestern, Liebigs Ann. Chem., 1979;2066-2075.
  • [21] Brand-Williams W, Cuvelier ME, Berset C. Use of a Free Radical Method to Evaluate Antioxidant Activity. LWT—Food Sci. Technol., 1995;28:25–30.
  • [22] Decker EA, Welch B. Role of Ferritin as a Lipid Oxidation Catalyst in Muscle Food. J. Agric. Food Chem., 1990;38:674–677.
  • [23] Oyaizu M. Studies on Product of Browning Reaction Prepared from Glucose Amine. Jpn. J. Nutr., 1986;44:307–315.
  • [24] Freshney RI. Culture of Animal Cells [6th (sixth) Edition], John Wiley & Sons, Inc., 2010; pp 732.
  • [25] van Meerloo J, Kaspers GJ. Cloos J. Cell sensitivity assays: the MTT assay. Methods in molecular biology (Clifton, N.J.), 2011;731:237–245.
  • [26] Llorent-Martinez EJ, Zengin G, Fernandez-de Cordova, ML, Bender O, Atalay A. Ceylan R., et al. Traditionally Used Lathyrus Species:Phytochemical Composition, Antioxidant Activity, Enzyme Inhibitory Properties,Cytotoxic Effects, and in silico Studies of L. czeczottianus and L.nissolia. Front. Pharmacol., 2017;8:63.
  • [27] Naydenova ED, Todorov PT, Topashka-Ancheva MN, Momekov G, Yordanova TZ, Konstantinov SM, et al. Novel N (phosphonomethyl) glycine derivatives: Design, characterization and biological activity, Eur. J. Med. Chem., 2008;43:1199-1205.
  • [28] Matilla B, Mauriz JL, Culebras JM, González-Gallego J, González P. Glycine: a cell-protecting anti-oxidant nutrient, Nutr. Hosp., 2002;17(1):2-9.
  • [29] Ladas EJ, Jacobson JS, Kennedy DD, Teel K, Fleischauer A. Kelly KM. Antioxidants and cancer therapy: a systematic review, J Clin Oncol., 2004;1;22(3):517-28.

Antioxidant and cytotoxic activity studies of sulfur containing glycine imine derivatives MCF-7 and DLD-1 cell lines

Year 2021, Volume: 11 Issue: 1, 81 - 90, 31.03.2021
https://doi.org/10.33808/clinexphealthsci.787954

Abstract

Objective: To investigate the antioxidant and cytotoxic activities of sulfur-containing glycine imine derivatives MCF-7 (human breast
adenocarcinoma) and DLD-1 (colorectal adenocarcinoma) cell lines.

Methods: This study examined the antioxidant activities (25-200 µM) of sulfur-containing glycine imine derivatives via the DPPH, metal chelating and reduction methods. Furthermore the cytotoxic activity of MCF-7, MCF-12A (normal breast epithelial) and DLD-1, CCD-18CO (normal colon fibroblast) were examined with MTT (3-(4,5-Dimethylthiazol-2-yl)-2,5-Diphenyltetrazolium Bromide) and RTCA (Real-time Cell Analysis) assays.

Results: The antioxidant assay of the metal chelating activity showed significant results (71, 77 and 40% respectively) as compared to
knowing synthetic antioxidant (trolox; 95.45, EDTA; 97.06 %). Reducing activity was found to be very low compared to the standard compounds.Compounds were shown to be moderated by DPPH (2,2-Diphenyl-1-picrylhydrazyl) activity, and the IC50 value ranged from 91
to 150. The IC50 values (100 µM) of the MTT and RTCA analyses were similar.

Conclusion: The study showed that the compounds had selective and significant antioxidant activities, and we also found that they
had cytotoxic effects on MCF-7 and DLD-1 cells.

Project Number

FMB-BAP 18-0333

References

  • [1] Jemal A, Siegel R, Ward E, Hao Y. Cancer Statistics, CA. Cancer J Clin. 2008;58(2):71-96.
  • [2] Siegel RL, Miller KD, Jemal A. Cancer Statistics, CA Cancer J Clin. 2017;67(1):7-30.
  • [3] World Health Organization. WHO. What is cancer?. https://www.who.int/cancer/en/ (2018).
  • [4] Saip P, Keskin S, Özkan M, Kaplan MA, Aydoğan F, Demirağ GG, et al. The Access Rate to Dıagnosıs and Treatment Modalıtıes in Breast Cancer Patıents in Turkey; Multıcenter Observatıonal Study. J. Breast Health. 2011;7:109-117.
  • [5] Jemal A, Siegel R, Ward E, Hao Y, Xu J, Thu MJ. Cancer statistics, CA. Cancer J Clin 2009; 59:225-249.
  • [6] Vaya J, Aviram M. Nutritional Antioxidants: Mechanisms of Action, Analyses of Activities and Medical Applications Curr. Med. Chem. – Imm., Endoc. & Metab. Agents, 2001;1:99-117.
  • [7] Valadez-Vega C, Delgado-Olivares L, Morales González JA, Alanís García E, Villagomez Ibarra JR, Ramírez Moreno, E., et al. The role of natural antioxidants in cancer disease. En Morales-González JA.(Edi.), Oxidative Stress and Chronic Degenerative Diseases - a Role for Antioxidants. 2013;391-418.
  • [8] Ganapathy V. Protein digestion and absorption. In Physiology of the Gastrointestinal Tract (Fifth Edition), Chapter 59 - Protein Digestion and Absorption, 2012;1595-1623.
  • [9] Cheng SB, Liu HT, Chen SY, Lin PT, Lai CY.Huang, YC. Changes of oxidative stress, glutathione, and its dependent antioxidant enzyme activities in patients with hepatocellular carcinoma before and after tumor resection. PloS one, 2017;12(1):e0170016.
  • [10] Deters M, Siegers CP, Strubelt O. Influence of glycine on the damage induced in isolated perfused rat liver by five hepatotoxic agents. Toxicology, 1998;128:63–72.
  • [11] Vaillancourt VA, Larsen SD, Tanis SP, Burr JE, Connell MA, Cudahy, MM. et al. Synthesis and biological activity of aminoguanidine and diaminoguanidine analogues of the antidiabetic/antiobesity agent 3-guanidinopropionic acid. J. Med. Chem., 2001;44(8):1231-1248.
  • [12] Bruns H, Kazanavicius D, Schultze D, Saeedi MA. Yamanaka K, Strupas K, et al. Glycine inhibits angiogenesis in colorectal cancer: Role of endothelial cells. Amino Acids, 2016;48: 2549-2558.
  • [13] Mukwevho E, Ferreira Z, Ayeleso A. Potential Role of Sulfur-Containing Antioxidant Systems in Highly Oxidative Environments. Molecules, 2014;19:19376-19389.
  • [14] Santhilkumar R, Sengottuvelan M, Nalini N. Protective effect of glycine supplementation in the levels of lipid peroxidation, and antioxidant enzymes in the erythrocyte of rats with alcohol-induced liver injury. Cell Biochem. Funct. 2004;22:123–128.
  • [15] Lim E, Hong D, Park J, Joung Y, Darvin P, Kim S, et al. Methylsulfonylmethane Suppresses Breast Cancer Growth by Down-Regulating STAT3 and STAT5b Pathways, PloS one, 2012;7(4): e33361.
  • [16] Kong CS, Bak SS, Rhee SH, Rho CW, Kim NK. Fermentation properties of young radish Kimchi prepared using young radish cultivated in the soil containing sulfur and it's inhibitory effect on the growth of AGS human gastric adenocarcinoma cells. J Korean Soc Food Sci Nutr., 2006;35:158–163.
  • [17] Ha AW, Hong KH, Kim HS, Kim WK. Inorganic sulfur reduces cell proliferation by inhibiting of ErbB2 and ErbB3 protein and mRNA expression in MDA-MB-231 human breast cancer cells. Nutrit. Res. Pract., 2013;7(2):89–95.
  • [18] Georgiou D, Toutountzoglou V, Muir KW, Hadjipavlou-Litina D, Elemes Y. Synthesis of sulfur containing dihydro-pyrrolo derivatives and their biological evaluation as antioxidants. Bio. Med. Chem., 2012;20(17):5103-5109.
  • [19] Pelit E, Oikonomou K, Gul M, Georgiou D, Szafert S, Katsamakas S, Elemes Y. α-Amination and the 5-exo-trig cyclization reaction of sulfur-containing Schiff bases with N-phenyltriazolinedione and their anti-lipid peroxidation activity. Com. Ren. Chim., 2017;20(4):424-434.
  • [20] Hoppe D, Beckmann L. Metallierte Stickstoff‐Derivate der Kohlensäure in der organischen Synthese, XIII. Selektive Mono‐ und Dialkylierung von N‐[Bis(alkylthio)‐methylen]glycin‐ethylestern zum Aufbau von kettenverlängerten und α‐verzweigten α‐Aminosäureestern, Liebigs Ann. Chem., 1979;2066-2075.
  • [21] Brand-Williams W, Cuvelier ME, Berset C. Use of a Free Radical Method to Evaluate Antioxidant Activity. LWT—Food Sci. Technol., 1995;28:25–30.
  • [22] Decker EA, Welch B. Role of Ferritin as a Lipid Oxidation Catalyst in Muscle Food. J. Agric. Food Chem., 1990;38:674–677.
  • [23] Oyaizu M. Studies on Product of Browning Reaction Prepared from Glucose Amine. Jpn. J. Nutr., 1986;44:307–315.
  • [24] Freshney RI. Culture of Animal Cells [6th (sixth) Edition], John Wiley & Sons, Inc., 2010; pp 732.
  • [25] van Meerloo J, Kaspers GJ. Cloos J. Cell sensitivity assays: the MTT assay. Methods in molecular biology (Clifton, N.J.), 2011;731:237–245.
  • [26] Llorent-Martinez EJ, Zengin G, Fernandez-de Cordova, ML, Bender O, Atalay A. Ceylan R., et al. Traditionally Used Lathyrus Species:Phytochemical Composition, Antioxidant Activity, Enzyme Inhibitory Properties,Cytotoxic Effects, and in silico Studies of L. czeczottianus and L.nissolia. Front. Pharmacol., 2017;8:63.
  • [27] Naydenova ED, Todorov PT, Topashka-Ancheva MN, Momekov G, Yordanova TZ, Konstantinov SM, et al. Novel N (phosphonomethyl) glycine derivatives: Design, characterization and biological activity, Eur. J. Med. Chem., 2008;43:1199-1205.
  • [28] Matilla B, Mauriz JL, Culebras JM, González-Gallego J, González P. Glycine: a cell-protecting anti-oxidant nutrient, Nutr. Hosp., 2002;17(1):2-9.
  • [29] Ladas EJ, Jacobson JS, Kennedy DD, Teel K, Fleischauer A. Kelly KM. Antioxidants and cancer therapy: a systematic review, J Clin Oncol., 2004;1;22(3):517-28.
There are 29 citations in total.

Details

Primary Language English
Subjects Health Care Administration
Journal Section Articles
Authors

Seda Mesci 0000-0002-5440-302X

Melek Gül 0000-0002-0037-1202

Tuba Yıldırım 0000-0001-8575-4802

Project Number FMB-BAP 18-0333
Publication Date March 31, 2021
Submission Date August 30, 2020
Published in Issue Year 2021 Volume: 11 Issue: 1

Cite

APA Mesci, S., Gül, M., & Yıldırım, T. (2021). Antioxidant and cytotoxic activity studies of sulfur containing glycine imine derivatives MCF-7 and DLD-1 cell lines. Clinical and Experimental Health Sciences, 11(1), 81-90. https://doi.org/10.33808/clinexphealthsci.787954
AMA Mesci S, Gül M, Yıldırım T. Antioxidant and cytotoxic activity studies of sulfur containing glycine imine derivatives MCF-7 and DLD-1 cell lines. Clinical and Experimental Health Sciences. March 2021;11(1):81-90. doi:10.33808/clinexphealthsci.787954
Chicago Mesci, Seda, Melek Gül, and Tuba Yıldırım. “Antioxidant and Cytotoxic Activity Studies of Sulfur Containing Glycine Imine Derivatives MCF-7 and DLD-1 Cell Lines”. Clinical and Experimental Health Sciences 11, no. 1 (March 2021): 81-90. https://doi.org/10.33808/clinexphealthsci.787954.
EndNote Mesci S, Gül M, Yıldırım T (March 1, 2021) Antioxidant and cytotoxic activity studies of sulfur containing glycine imine derivatives MCF-7 and DLD-1 cell lines. Clinical and Experimental Health Sciences 11 1 81–90.
IEEE S. Mesci, M. Gül, and T. Yıldırım, “Antioxidant and cytotoxic activity studies of sulfur containing glycine imine derivatives MCF-7 and DLD-1 cell lines”, Clinical and Experimental Health Sciences, vol. 11, no. 1, pp. 81–90, 2021, doi: 10.33808/clinexphealthsci.787954.
ISNAD Mesci, Seda et al. “Antioxidant and Cytotoxic Activity Studies of Sulfur Containing Glycine Imine Derivatives MCF-7 and DLD-1 Cell Lines”. Clinical and Experimental Health Sciences 11/1 (March 2021), 81-90. https://doi.org/10.33808/clinexphealthsci.787954.
JAMA Mesci S, Gül M, Yıldırım T. Antioxidant and cytotoxic activity studies of sulfur containing glycine imine derivatives MCF-7 and DLD-1 cell lines. Clinical and Experimental Health Sciences. 2021;11:81–90.
MLA Mesci, Seda et al. “Antioxidant and Cytotoxic Activity Studies of Sulfur Containing Glycine Imine Derivatives MCF-7 and DLD-1 Cell Lines”. Clinical and Experimental Health Sciences, vol. 11, no. 1, 2021, pp. 81-90, doi:10.33808/clinexphealthsci.787954.
Vancouver Mesci S, Gül M, Yıldırım T. Antioxidant and cytotoxic activity studies of sulfur containing glycine imine derivatives MCF-7 and DLD-1 cell lines. Clinical and Experimental Health Sciences. 2021;11(1):81-90.

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