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Kolşisin’in MCF-7 insan meme adenokarsinoma hücrelerinde hücre döngüsü tutulumu ve MMP-2 mRNA ifade seviyesi üzerine etkisi

Year 2018, Volume: 75 Issue: 3, 239 - 244, 01.09.2018

Abstract

Amaç: Kolşisin, trisiklik alkaloid bir ilaç olup klinikte anti-enflamatuvar etkisinden dolayı yaygın olarak kullanılmaktadır. Kolşisin uygun konsantrasyonlarda oral yolla kullanılmakta iken yüksek konsantrasyonlarda toksik etki gösterdiği tespit edilmiştir. Bu nedenle, kanser araştırmalarında düşük doz kolşisinin etki mekanizmaları üzerine çalışmalar yapılmaktadır. Matriks metalloproteinaz-2 MMP-2 , matriks metalloproteinaz enzim ailesinin bir üyesi olup kanserde ifade seviyesinin arttığı ve ekstrasellüler matriksi yıkıma uğratarak kanser hücrelerinin metastazına neden olduğu bildirilmiştir. MMP’lerin bu önemli etkisi nedeni ile kanser hastalığında metastazın önlenmesi amacıyla çeşitli bileşiklerin MMP üzerine inhibitör etkisinin değerlendirilmesi kanser araştırmalarında önemli yer tutmaktadır. Bu çalışmada, kolşisinin, MCF-7 insan meme adenokarsinoma hücresinde hücre döngüsü tutulumu ve metastazda önemli rol oynadığı bilinen MMP-2 protein ifadesi üzerine etkisinin araştırılması amaçlanmıştır. Yöntem: Çalışmada, MCF-7 insan meme adenokarsinoma hücreleri kullanılmıştır ATCC, HTB22 . Hücrelere 0.1, 10 ve 100 μg/ml konsantrasyonlarda kolşisin uygulanmış ve hücre canlılığı analizi MTT testi ile yapılmıştır. Kolşisin’in hücre döngüsü tutulumu üzerine etkisi analiz edilmiş ve G0/G1, S ve G2/M döngüsündeki hücre populasyonları yüzde % olarak ifade edilmiştir. Kolşisin’in MMP-2 mRNA ifade seviyesi üzerine etkisi ise gerçek zamanlı PCR qRT-PCR yöntemi ile tayin edilmiştir. Bulgular: 10 ve 100 μg/ml konsantrasyonlarda Kolşisin MCF-7 meme kanser hücresinin canlılığını istatistiksel olarak anlamlı derecede inhibe etmiştir. Kolşisin’in tüm konsantrasyonlarda hücre döngüsünü G2/M fazında inhibe ettiği ve MMP-2 geninin ifade seviyesini anlamlı olarak azalttığı saptanmıştır p

References

  • Angelidis C, Kotsialou Z, Kossyvakis C, Vrettou AR, Zacharoulis A, Kolokathis F, et al. Colchicine Pharmacokinetics and Mechanism of Action. Curr Pharm Des, 2018; doi: 10.2174/1381612824666180123110042.
  • Slobodnick A, Shah B, Pillinger MH, Krasnokutsky S. Colchicine: Old and New. Am J Med, 2015; 128(5): 461-70.
  • Ghawanmeh AA, Chong KF, Sarkar SM, Bakar MA, Othaman R, Khalid RM. Colchicine prodrugs and codrugs: Chemistry and bioactivities. Eur J Med Chem, 2018; 144: 229-42.
  • Liantinioti G, Argyris AA, Protogerou AD, Vlachoyiannopoulos P. The role of colchicine in the treatment of autoinflammatory diseases. Curr Pharm Des, 2018; doi: 10.2174/1381612824666180 116095658.
  • Leung YY, Yao Hui LL, Kraus VB. Colchicine-Update on mechanisms of action and therapeutic uses. Semin Arthritis Rheum, 2015; 45(3): 341-50.
  • Marinaki S, Skalioti C, Boletis JN. Colchicine in renal diseases: present and future. Curr Pharm Des, 2018; doi: 10.2174/1381612824666180123101313.
  • Dubey KK, Kumar P, Labrou NE, Shukla P. Biotherapeutic potential and mechanisms of action of colchicine. Crit Rev Biotechnol, 2017; 37(8): 1038-47.
  • Lin ZY, Wu CC, Chuang YH, Chuang WL. Anti-cancer mechanisms of clinically acceptable colchicine concentrations on hepatocellular carcinoma. Life Sci, 2013; 93: 323-28.
  • Wu CC, Lin ZY, Kuoc CH, Chuang WL. Clinically acceptable potential for the palliative treatment of human cholangiocarcinoma. Kaohsiung J Med Sci, 2015; 31: 229-34.
  • concentrations have
  • Lin ZY, Kuo CH, Wu DC, Chuang WL. Anticancer effects of clinically acceptable colchicine concentrations on human gastric cancer cell lines. Kaohsiung J Med Sci, 2016; 32: 68-73.
  • Risinger AL, Giles FJ, Mooberry SL. Microtubule dynamics as a target in oncology. Cancer Treat Rev, 2009; 35(3): 255-61.
  • Jordan MA, Wilson L. Microtubules as a target for anticancer drugs. Nat Rev Cancer, 2004.; 4(4): 253- 65.
  • Kumar A, Singh B, Mahajan G, Sharma PR, Bharate SB, Mintoo MJ, et al. A novel colchicine-based microtubule inhibitor exhibits potent antitumor activity by inducing mitochondrial mediated apoptosis in MIA PaCa-2 pancreatic cancer cells. Tumour Biol, 2016; 37(10): 13121-136.
  • Cho JH, Joo YH, Shin EY, Park EJ, Kim MS. Anticancer Effects of Colchicine on Hypopharyngeal Cancer. Anticancer Res, 2017; 37(11): 6269-280.
  • Kumar A, Singh B, Sharma PR, Bharate SB, Saxena AK, Mondhe DM. A novel microtubule depolymerizing colchicine analogue triggers apoptosis and autophagy in HCT-116 colon cancer cells. Cell Biochem Funct, 2016; 34(2): 69-81.
  • Huang Z, Xu Y, Peng W. Colchicine induces apoptosis in HT29 human colon cancer cells via the AKT and c-Jun N-terminal kinase signaling pathways. Mol Med Rep, 2015; 12(4): 5939-944.
  • Sun Y, Lin X, Chang H. Proliferation inhibition and apoptosis of breast cancer MCF-7 cells under the influence of colchicine. J BUON, 2016; 21(3): 570- 75.
  • Bhattacharya S, Das A, Datta S, Ganguli A, Chakrabarti G. Colchicine induces autophagy and senescence in lung cancer cells at clinically admissible concentration: potential use of colchicine in combination with autophagy inhibitor in cancer therapy. Tumour Biol, 2016; 37(8): 10653- 664.
  • Arrieta O, Rodriguez-Diaz JL, Rosas-Camargo V, Morales-Espinosa D, Ponce de Leon S, Kershenobich D, et al. Colchicine delays the development of hepatocellular carcinoma in patients with hepatitis virus-related liver cirrhosis. Cancer, 2006; 107(8): 1852-858.
  • Kuo MC, Chang SJ, Hsieh MC. Colchicine Significantly Reduces Incident Cancer in Gout Male Patients: A 12-Year Cohort Study. Medicine (Baltimore), 2015; 94(50): e1570
  • Murphy, G. 2008. “The ADAMs: signalling scissors in the tumour microenvironment”, Nat Rev Cancer, 8, 932-941
  • Deryugina, I.E., Quigley, P.J. 2006. “Matrix metalloproteinases and tumor metastasis”, Cancer Metastasis Rev, 25, 9-34
  • Coussens, L.M., Fingleton, B., Matrisian, L.M. 2002. “Matrix Metalloproteinase Inhibitors and Cancer: Trials and Tribulations”, Science, 295, 2387-2392

Effects of colchicine on cell cycle arrest and MMP-2 mRNA expression in MCF-7 breast adenocarcinoma cells

Year 2018, Volume: 75 Issue: 3, 239 - 244, 01.09.2018

Abstract

Objective: Colchicine is a tricyclic alkaloid drug and it’s been clinically used for a long time because of its anti-inflammatory effects. While colchicine has been safely used in oral applications, it’s been demonstrated that colchicine is toxic at higher concentrations. So, the mechanism of effects of low dose colchicine has been studied in cancer related researches. Matrix metalloproteinase-2 MMP-2 is a member of matrix metalloproteinase enzyme family and it’s been demonstrated that MMP-2 expression is increased in cancer and it causes a metastasis of cancer cells through degradation of extracellular matrix. Because of this important effect of MMPs, the studies related to develop MMP inhibitor compounds have great importance in cancer investigations. At present study, it’s aimed to investigate the effects of colchicine on cell cycle arrest and MMP-2 mRNA expression in MCF-7 human breast cancer cells. Methods: In the study, MCF-7 human breast adenocarcinoma cells were purchased from ATCC. Cells were treated with 0.1, 10 ve 100 μg/ml colchicine and cell viability was determined via MTT assay. The effect of colchicine on cell cycle arrest was determined by Muse Cell Analyzer and the percent of cell populations at G0/G1, S and G2/M cycles were identified. The effect of colchicine on MMP-2 mRNA expression has been performed by real-time PCR qRTPCR analysis. Results: Colchicine has significantly inhibited cell viability at 10 and 100 μg/ml concentrations. It’s been also demonstrated that colchicine has induced a cell cycle arrest at G2/M phase and downregulated MMP-2 mRNA expression of MCF-7 cells in all treated concentration p

References

  • Angelidis C, Kotsialou Z, Kossyvakis C, Vrettou AR, Zacharoulis A, Kolokathis F, et al. Colchicine Pharmacokinetics and Mechanism of Action. Curr Pharm Des, 2018; doi: 10.2174/1381612824666180123110042.
  • Slobodnick A, Shah B, Pillinger MH, Krasnokutsky S. Colchicine: Old and New. Am J Med, 2015; 128(5): 461-70.
  • Ghawanmeh AA, Chong KF, Sarkar SM, Bakar MA, Othaman R, Khalid RM. Colchicine prodrugs and codrugs: Chemistry and bioactivities. Eur J Med Chem, 2018; 144: 229-42.
  • Liantinioti G, Argyris AA, Protogerou AD, Vlachoyiannopoulos P. The role of colchicine in the treatment of autoinflammatory diseases. Curr Pharm Des, 2018; doi: 10.2174/1381612824666180 116095658.
  • Leung YY, Yao Hui LL, Kraus VB. Colchicine-Update on mechanisms of action and therapeutic uses. Semin Arthritis Rheum, 2015; 45(3): 341-50.
  • Marinaki S, Skalioti C, Boletis JN. Colchicine in renal diseases: present and future. Curr Pharm Des, 2018; doi: 10.2174/1381612824666180123101313.
  • Dubey KK, Kumar P, Labrou NE, Shukla P. Biotherapeutic potential and mechanisms of action of colchicine. Crit Rev Biotechnol, 2017; 37(8): 1038-47.
  • Lin ZY, Wu CC, Chuang YH, Chuang WL. Anti-cancer mechanisms of clinically acceptable colchicine concentrations on hepatocellular carcinoma. Life Sci, 2013; 93: 323-28.
  • Wu CC, Lin ZY, Kuoc CH, Chuang WL. Clinically acceptable potential for the palliative treatment of human cholangiocarcinoma. Kaohsiung J Med Sci, 2015; 31: 229-34.
  • concentrations have
  • Lin ZY, Kuo CH, Wu DC, Chuang WL. Anticancer effects of clinically acceptable colchicine concentrations on human gastric cancer cell lines. Kaohsiung J Med Sci, 2016; 32: 68-73.
  • Risinger AL, Giles FJ, Mooberry SL. Microtubule dynamics as a target in oncology. Cancer Treat Rev, 2009; 35(3): 255-61.
  • Jordan MA, Wilson L. Microtubules as a target for anticancer drugs. Nat Rev Cancer, 2004.; 4(4): 253- 65.
  • Kumar A, Singh B, Mahajan G, Sharma PR, Bharate SB, Mintoo MJ, et al. A novel colchicine-based microtubule inhibitor exhibits potent antitumor activity by inducing mitochondrial mediated apoptosis in MIA PaCa-2 pancreatic cancer cells. Tumour Biol, 2016; 37(10): 13121-136.
  • Cho JH, Joo YH, Shin EY, Park EJ, Kim MS. Anticancer Effects of Colchicine on Hypopharyngeal Cancer. Anticancer Res, 2017; 37(11): 6269-280.
  • Kumar A, Singh B, Sharma PR, Bharate SB, Saxena AK, Mondhe DM. A novel microtubule depolymerizing colchicine analogue triggers apoptosis and autophagy in HCT-116 colon cancer cells. Cell Biochem Funct, 2016; 34(2): 69-81.
  • Huang Z, Xu Y, Peng W. Colchicine induces apoptosis in HT29 human colon cancer cells via the AKT and c-Jun N-terminal kinase signaling pathways. Mol Med Rep, 2015; 12(4): 5939-944.
  • Sun Y, Lin X, Chang H. Proliferation inhibition and apoptosis of breast cancer MCF-7 cells under the influence of colchicine. J BUON, 2016; 21(3): 570- 75.
  • Bhattacharya S, Das A, Datta S, Ganguli A, Chakrabarti G. Colchicine induces autophagy and senescence in lung cancer cells at clinically admissible concentration: potential use of colchicine in combination with autophagy inhibitor in cancer therapy. Tumour Biol, 2016; 37(8): 10653- 664.
  • Arrieta O, Rodriguez-Diaz JL, Rosas-Camargo V, Morales-Espinosa D, Ponce de Leon S, Kershenobich D, et al. Colchicine delays the development of hepatocellular carcinoma in patients with hepatitis virus-related liver cirrhosis. Cancer, 2006; 107(8): 1852-858.
  • Kuo MC, Chang SJ, Hsieh MC. Colchicine Significantly Reduces Incident Cancer in Gout Male Patients: A 12-Year Cohort Study. Medicine (Baltimore), 2015; 94(50): e1570
  • Murphy, G. 2008. “The ADAMs: signalling scissors in the tumour microenvironment”, Nat Rev Cancer, 8, 932-941
  • Deryugina, I.E., Quigley, P.J. 2006. “Matrix metalloproteinases and tumor metastasis”, Cancer Metastasis Rev, 25, 9-34
  • Coussens, L.M., Fingleton, B., Matrisian, L.M. 2002. “Matrix Metalloproteinase Inhibitors and Cancer: Trials and Tribulations”, Science, 295, 2387-2392
There are 24 citations in total.

Details

Primary Language English
Journal Section Research Article
Authors

Filiz Bakar Ateş This is me

Nuri Özmen This is me

Ecem Kaya Sezginer This is me

Emin Emre Kurt This is me

Publication Date September 1, 2018
Published in Issue Year 2018 Volume: 75 Issue: 3

Cite

APA Ateş, F. B., Özmen, N., Sezginer, E. K., Kurt, E. E. (2018). Effects of colchicine on cell cycle arrest and MMP-2 mRNA expression in MCF-7 breast adenocarcinoma cells. Türk Hijyen Ve Deneysel Biyoloji Dergisi, 75(3), 239-244.
AMA Ateş FB, Özmen N, Sezginer EK, Kurt EE. Effects of colchicine on cell cycle arrest and MMP-2 mRNA expression in MCF-7 breast adenocarcinoma cells. Turk Hij Den Biyol Derg. September 2018;75(3):239-244.
Chicago Ateş, Filiz Bakar, Nuri Özmen, Ecem Kaya Sezginer, and Emin Emre Kurt. “Effects of Colchicine on Cell Cycle Arrest and MMP-2 MRNA Expression in MCF-7 Breast Adenocarcinoma Cells”. Türk Hijyen Ve Deneysel Biyoloji Dergisi 75, no. 3 (September 2018): 239-44.
EndNote Ateş FB, Özmen N, Sezginer EK, Kurt EE (September 1, 2018) Effects of colchicine on cell cycle arrest and MMP-2 mRNA expression in MCF-7 breast adenocarcinoma cells. Türk Hijyen ve Deneysel Biyoloji Dergisi 75 3 239–244.
IEEE F. B. Ateş, N. Özmen, E. K. Sezginer, and E. E. Kurt, “Effects of colchicine on cell cycle arrest and MMP-2 mRNA expression in MCF-7 breast adenocarcinoma cells”, Turk Hij Den Biyol Derg, vol. 75, no. 3, pp. 239–244, 2018.
ISNAD Ateş, Filiz Bakar et al. “Effects of Colchicine on Cell Cycle Arrest and MMP-2 MRNA Expression in MCF-7 Breast Adenocarcinoma Cells”. Türk Hijyen ve Deneysel Biyoloji Dergisi 75/3 (September 2018), 239-244.
JAMA Ateş FB, Özmen N, Sezginer EK, Kurt EE. Effects of colchicine on cell cycle arrest and MMP-2 mRNA expression in MCF-7 breast adenocarcinoma cells. Turk Hij Den Biyol Derg. 2018;75:239–244.
MLA Ateş, Filiz Bakar et al. “Effects of Colchicine on Cell Cycle Arrest and MMP-2 MRNA Expression in MCF-7 Breast Adenocarcinoma Cells”. Türk Hijyen Ve Deneysel Biyoloji Dergisi, vol. 75, no. 3, 2018, pp. 239-44.
Vancouver Ateş FB, Özmen N, Sezginer EK, Kurt EE. Effects of colchicine on cell cycle arrest and MMP-2 mRNA expression in MCF-7 breast adenocarcinoma cells. Turk Hij Den Biyol Derg. 2018;75(3):239-44.