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Detection of the Calcium and ATP Role in Apoptosis of Retinoblastoma Culture Cells through Caspase-3 Expression
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Retinoblastoma is a malignant retinal tumor associated with apoptotic deregulation. Retinoblastoma cells are sensitive to NK cells. These cells can stimulate apoptosis. Apoptosis in retinoblastoma occurs in the early phase and is paradoxical. The increasing amounts of Bcl-2 and Caspase-3 as apoptotic executors are inversely proportional to apoptosis. Calcium and ATP as second messengers and signaling molecules play role in mediating cell responses including retinoblastoma cell development and death. Apoptosis requires sufficient energy from ATP and its mediated by Calcium. This study aimed to perceive the effects of Calcium and ATP in the process of retinoblastoma cell death through Caspase-3 pathway. The subjects were poorly differentiated retinoblastoma cell cultures treated with NK cells (treatment group) compared to those which were not exposed to NK cells (control group). Through the cell flowcytometry test that expresses Caspase-3 and apoptosis is calculated, meanwhile the levels of Calcium and ATP activity produced during the apoptosis process are quantitatively calculated. Examination of ATP activity uses a colorimetric method while the calcium content is calculated using a clinical chemistry system. Calcium and ATP were negatively correlated at 27.4% (p <0.05). ATP also showed a very significant negative correlation of 75.8% (p <0.01) against Caspase-3 and is significantly positively correlated with apoptosis of 46.8% (p,0.05). Whereas Caspase-3 is negatively correlated with apoptosis by 46.6% (p <0.05). In the Caspase-3 pathway, allogeneic NK cell administration in retinoblastoma cells increases the level of Calcium which plays a role in the early phase apoptosis process, whereas ATP which was formed is insufficient to cause maximal apoptosis due to extracellular calcium entry into NK cells. Extracellular ATP does not play a role in the induction of apoptosis in retinoblastoma cells treated with NK cells.
Keywords
Allogeneic NK Cells, Caspase-3, Apoptosis, Calcium, ATP.
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- Stewart, BW and Wild, CP. World Cancer Report 2014. 2014. International Agency for Research on Cancer, Lyon
- Dharmawidiarini, D, Prijanto, Soebagjo, HD. Ocular survival rate penderita retinoblastoma yang telah dilakukan enukleasi atau eksenterasi di RSUD Dr. Soetomo Surabaya. Media Jurnal Oftamlologi Indonesia. 2010. Vol.7. No.3.
- Soebagjo, HD, R Prastyani, H Sujuti, D Lyrawati and SB Sumitro. Profile of Retinoblastoma in East Java, Indonesia. World Journal of Medicine and Medical Science Research. 2013. 1(3): 051-056
- Ravi B, Sivabalan T. A study to evaluate the Quality of life in Head and Neck Cancer Patients admitted in Pravara Rural Hospital, Loni (Bk). Asian J. Nursing Edu. and Research. 2013; 3(1): 21-4
- Kerimoğglu H, Kiratli H, Dinçtürk AA, Söylemezoğlu F, Bilgiç S. Quantitative analysis of proliferation, apoptosis, and angiogenesis in retinoblastoma and their association with the clinicopathologic parameters. Jpn J Ophthalmol. 2003;47: 565–571.
- Davis, CT, Rizzieri, D. Immunotherapeutic applications of NK cells. Pharmaceuticals. 2015. 8(2), 250-256. doi:10.3390/ph8020250.
- Ishikawa E, Tsuboi K, Saijo K, Harada H, Takano S, Nose T, et al. Autologous natural killer cell therapy for human recurrent malignant glioma. Anticancer Res 2004;24: 1861–71.
- Knudson Jr., AG. Clinical Ophthalmic Oncology, Saunders Elesevier, Philadelphia. 2007. (335): pp1-16.
- Sitorus, RS, S Gumay, PV Der Valk. The apoptosis paradox in retinoblastoma. Natural compounds and their role in apoptotic cell signaling pathways. Ann.N.Y. Acad.Sci. 2009. 1171: 77-86.
- Soebagjo, HD, Fatmariyanti S, and Lutfi D. Effectiveness of Natural Killer (NK) cells in pheripheral blood stem cell towards expression of EZH2, Ki-67 and apoptosis in Retinoblastoma (RB) cells culture. Medicine Science, 2015. vol.04, pp.1-17.
- Soebagjo, HD, Kusumastuti F, Jaya PR, Fatmariyanti S. Pengaruh sel Natural Killer Alogenik terhadap apoptosis, Bcl-2 dan Caspase-3 sel retinoblastoma. 2016. Fakultas Kedokteran, Universitas Airlangga.
- Böyum A. Isolation of leucocytes from human blood. Further observations. Methylcellulose, dextran, and ficoll as erythrocyte aggregating agents. Scand J Clin Lab Invest Suppl. 1968; 97:31-50.
- Jangde R An Overview of Resealed Erythrocyte for Cancer Therapy. Asian J. Res. Pharm. Sci. 2011; 1(4):83-92.
- Hu P, Hegde M, Lennon PA. Modern Clinical Molecular Techniques. 2012. Springer, New York.
- Sava, L, S Pillai, U More, A Sontakke. Serum calcium measurement: total versus free (ionized) calcium. Indian Journal of Clinical Biochemistry. 2005.20(2): 158-161.
- Bowen, Raffick AR and Alan T Remaley. Interferences from blood collection tube components on clinical chemistry assays. Biochemia Medica. 2014. 24(1):31–44 http://dx.doi.org/10.11613/BM.2014.006
- Wang, J, L Wang, X Liu, Z Liang, S Song, W Li, G Li, C Fan. A Gold Nanoparticle‐Based Aptamer Target Binding Readout for ATP Assay. Communication. Advanced Materials. 2007. 19(22): 3943-3946. https://doi.org/10.1002/adma.200602256
- Méry, B, JB Guy, A Vallard, S Espenel, D Ardail, C Rodriguez-Lafrasse, C Rancoule and N Magné. In Vitro Cell Death Determination for Drug Discovery: A Landscape Review of Real Issues. Journal of Cell Death. 2017. 1–8
- Afroz A, Haque T, Talukder MU, Islam SMA. Spectrophotometric Estimation of Rosuvastatin Calcium and Glimepiride in Tablet Dosage Form. Asian J. Pharm. Ana. 2011; 1(4): 74-78.
- Takadera T, Ohtsuka M, Aoki H. Chelation of extracellular calcium-induced cell death was prevented by glycogen synthase kinase-3 inhibitors in PC12 cells. Cell Mol Neurobiol. 2010. Mar;30(2):193-8. doi: 10.1007/s10571-009-9442-y.
- Voccoli V, Tonazzini, Signore G, Caleo M, Cecchini M. Role of extracellular calcium and mitochondrial oxygen species in psychosine-induced oligodendrocyte cell death. Cell Death & Disease. 2014. 5e1529. doi: 10.1038/cddis.2014.483.
- Nguyen T, Johnston S., Clarke L., Smith P, Staines D, Marshall-Gradisnik S. Impaired calcium mobilization in natural killer cells from chronic fatigue syndrome/myalgic encephalomyelitis patients is associated with transient receptor potential melastatin 3 ion channels. Clinical &Experimental Immunology. 2017. Feb; 187(2): 284-293. Doi: 10.1111/cei.12882.
- Bagilkar VV, Patil AA. Benefits of Stem Cells in Pediatrics. International Journal of Nursing Education and Research. 2017; 5(4): 377-380.
- Zheng LM, Zychlinsky A, Liu C-C, Ojcius DM, Ding-E Young J. Extracellular ATP as a trigger for apoptosis or Programmed Cell Death. The Journal of Cell Biology. 1991. 112(2): 279-288.
- Ganguly S. Effect of ATPase/ATP Synthetase inhibitors on As (III) biosorption by Aspergillus niger X300. Research J. Pharmacology and Pharmacodynamics. 2013; 5(4): 205-206.
- Shenoy AM, Sidner RA, Brahmi Z. Signal transduction in cytotoxic lymphocytes: decreased calcium influx in NK cell inactivated with sensitive target cells. Cell Immunol. 1993. 147(2):294-301.
- Lin K, Chattopadhyay N, Bai M, Alvarez R, Dang CV, Baraban JM, Brown EM, Ratan RR. Elevated Extracellular Calcium Can Prevent Apoptosis via the Calcium-Sensing Receptor. Biochemical and biophysical research communications. 1998. Vol.249, Issue 2, pp 325-331.
- Paola AM, Eduardo CC, Jessica N, Aline B, Danielle BS. Adenosine uptake is the major effector of extracellular ATP toxicity in human cervical cancer cells. Mol. Biol. Cell. 2014. Oct 1; 25(19): 2905-2918. doi: 10.1091/mbc. E14-01-0042.
- Deli, T and Csernoch L. Extracellular ATP and cancer: an overview with special reference to P2 purinergic receptors. Pathol. Oncol. Res. 2008.14: 219-231.
- Jangde R. Matrix metalloproteinase: An overview. Research J. Science and Tech. 2011; 3(6): 304-310.
- Stagg J and Smyth MJ. Extracellular adenosine triphosphate and adenosine in cancer. Oncogene. 2010. 29: 5346-5358. doi: 10.1038/onc.2010.292.
- Jiang, Jean X, MA Riquelme, and JZ Zhou. ATP, a double-edged sword in cancer. Oncoscience. 2015. Vol.2, No.8. 1-2.
- Pradeep S, Swati C, Ravindra D, Shweta P, Shilpi C, Tanushree C. Nanoparticles- Drug Delivery System in Cancer Therapy. Research J. Pharma. Dosage Forms and Tech. 2011; 3(2): 33-41.
- Sorrentino R, Pinto A, and Morello S. The adenosinergic system in cancer. OncoImmunology, 2013. Vol.2, Issue 1. doi: 10-4161/onci.22448.
- Antonioli L, Hasko G, Fornai M, Colucci R, Blandizzi C. Adenosine pathway and cancer: where do we go from here? Expert Opin Ther Targets. 2014.18(9): 973-7. doi: 10.1517/14728222.2014.925883.
- Cheng, M, Chen Y, Xiao W, Sun R. NK cell-based immunotherapy for malignant diseases. Cell Mol Immunol, 2013.May; 10(3); 230-52. doi: 10.1038/cmi.2013.10.
- Poggi, A, C Prevosto, AM Massaro, S Negrini, S Urbani, I Pierri, R Saccardi, M Gobbi, and MR Zocchi. Interaction between Human NK Cells and Bone Marrow Stromal Cells Induces NK Cell Triggering: Role of NKp30 and NKG2D Receptors. J Immunol. 2005.175(10) 6352-6360; DOI: https://doi.org/10.4049/jimmunol.175.10.6352
- Dwivedi N, Dwivedi B, Mishra S, Shukla Y. Lupeol Induced Apoptosis in Human Lung Cancer Cell Line: A Flow Cytometry Study. Research Journal of Pharmacology and Pharmacodynamics. 2014; 6(4): 197-203.
- Pinkoski MJ, Waterhouse NJ, Heibein JA, Wolf BB, Kuwana T, et al., Granzyme B-mediated apoptosis proceeds predominantly through a Bcl-2 inhibitatable mitochondrial pathway. J Biol Chem. 2001. Apr 13; 276(15): 1260-7. doi: 10.1074/jbc.M009038200.
- Verhagen AM, Coulson EJ, Vaux DL. Inhibitor of apoptosis proteins and their relatives: IAPs and other BIRPs. Genome Biol. 2001. 2(7); Reviews3009. PMID: 11516343. PMCID: PMC139420.
- Adrain C, Creagh EM, Martin SJ. Apoptosis-associated release of Smac/DIABLO from mitochondria requires active caspases and is blocked by Bcl-2. EMBO J. 2001. Dec 3: 20(23): 6627-6636. doi: 10.1093/emboj/20.23.6627.
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