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Articulatin-D induces apoptosis via activation of caspase-8 in acute T-cell leukemia cell line

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Abstract

Leukemia is among the most aggressive and prevalent human malignant carcinoma. Chemotherapy is the preferred therapeutic strategy; however, recurrence of cancer and non-selective cytotoxicity are the major concerns. Unlike synthetic chemotherapeutic agents, mistletoe ribosome-inactivating protein (RIP) displays anti-tumor function in various types of cancers. However, its effect on leukemia cells is little explored. In this study, we assessed the impact of Viscum articulatum RIP (Articulatin-D) on the survival of acute T-cell leukemia cells and the involved molecular and cellular mechanisms. Cell proliferation assay showed that Articulatin-D suppressed the viability of leukemia cells selectively. We further confirmed that the elevation of mitochondrial membrane potential and exposure of phosphatidylserine are the early events of apoptosis induction in Articulatin-D-treated Jurkat cells. Subsequently, we found that Articulatin-D treatment induces apoptosis in Jurkat cells in a time- and concentration-dependent manner. In conclusion, we provided evidence that Articulatin-D efficiently activates caspase-8 involved in extrinsic pathway of apoptosis induction, which ultimately results in caspase-3-dependent DNA fragmentation of Jurkat cells. Further evaluation of Articulatin-D in cell culture and animal models may provide novel information on selective cytotoxicity to acute T-cell leukemia and its involvement in targeting tumor cell survival pathways.

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References

  1. Torre LA, Bray F, Siegel RL, Ferlay J, Lortet-tieulent J, Jemal A (2015) Global cancer statistics, 2012. CA Cancer J Clin 65:87–108

    Article  PubMed  Google Scholar 

  2. Gaynon PS (2005) Childhood acute lymphoblastic leukaemia and relapse. Br J Haematol 131:579–587

    Article  PubMed  Google Scholar 

  3. Lichtman MA (2008) Battling the hematological malignancies: the 200 years’ war. Oncologist 13:126–138

    Article  PubMed  Google Scholar 

  4. Voliotis D, Diehl V (2002) Challenges in treating hematologic malignancies. Semin Oncol 29:30–39

    Article  CAS  PubMed  Google Scholar 

  5. Siegel R, Desantis C, Virgo K, Stein K, Mariotto A, Smith T, Cooper D, Gansler T, Lerro C, Fedewa S, Lin C, Leach C, Cannady RS, Cho H, Scoppa S, Hachey M, Kirch R, Jemal A, Ward E (2013) Cancer treatment and survivorship statistics, 2012. CA Cancer J Clin 62:220–241

    Article  Google Scholar 

  6. Vagace JM, Gervasini G (2010) Chemotherapy toxicity in patients with acute leukemia—The scientist’s perspective and challenge. Available from http://www.intechopen.com/books/acute-leukemia-the-scientist-sperspective-and-challenge/chemotherapy-toxicity-in-patients-with-acute-leukemia

  7. Pryme IF, Bardocz S, Pusztai A, Ewen SWB (2006) Suppression of growth of tumour cell lines in vitro and tumours in vivo by mistletoe lectins. Histol Histopathol 21:285–299

    CAS  PubMed  Google Scholar 

  8. Grossarth-Maticek R, Ziegler R (2006) Randomised and non-randomised prospective controlled cohort studies in matched-pair design for the long-term therapy of breast cancer patients with a mistletoe preparation (Iscador): a re-analysis. Eur J Med Res 11:485–495

    CAS  PubMed  Google Scholar 

  9. Goebell PJ, Thomas O, Julia S, Herbert R (2002) Evaluation of an unconventional treatment modality with Mistletoe lectin to prevent recurrence of superficial bladder cancer: a randomized phase II trial. J Urol 168:72–75

    Article  PubMed  Google Scholar 

  10. Bar-Sela G, Haim N (2004) Abnoba-viscum (Mistletoe extract) in metastatic colorectal carcinoma resistant to 5-fluorouracil and leucovorin-based chemotherapy. Med Oncol 21:251–254

    Article  CAS  PubMed  Google Scholar 

  11. Bar-Sela G, Wollner M, Hammer L, Agbarya A, Dudnik E, Haim N (2013) Mistletoe as complementary treatment in patients with advanced non-small-cell lung cancer treated with carboplatin-based combinations: a randomised phase II study. Eur J Cancer 49:1058–1064

    Article  CAS  PubMed  Google Scholar 

  12. Horneber M, Bueschel G, Huber R, Linde K, Rostock M (2010) Mistletoe therapy in oncology. Cochrane Libr 4:4–6

    Google Scholar 

  13. Stirpe F, Battelli MG (2006) Ribosome-inactivating proteins: progress and problems. Cell Mol Life Sci 63:1850–1866

    Article  CAS  PubMed  Google Scholar 

  14. Büssing A (1996) Induction of apoptosis by the mistletoe lectins: a review on the mechanisms of cytotoxicity mediated by Viscum album L. Apoptosis 1:25–32

    Article  Google Scholar 

  15. Mishra V, Sharma RS, Yadav S, Babu CR, Singh TP (2004) Purification and characterization of four isoforms of Himalayan mistletoe ribosome-inactivating protein from Viscum album having unique sugar affinity. Arch Biochem Biophys 423:288–301

    Article  CAS  PubMed  Google Scholar 

  16. Mishra V, Ethayathulla AS, Sharma RS, Yadav S, Krauspenhaar R, Betzel C, Babu CR, Singh TP (2004) Structure of a novel ribosome-inactivating protein from a hemi-parasitic plant inhabiting the northwestern Himalayas. Acta Crystallogr D Biol Crystallogr 60:2295–2304

    Article  PubMed  Google Scholar 

  17. Mishra V, Bilgrami S, Sharma RS, Kaur P, Yadav S, Krauspenhaar R, Betzel C, Voelter W, Babu CR, Singh TP (2005) Crystal structure of himalayan mistletoe ribosome-inactivating protein reveals the presence of a natural inhibitor and a new functionally active sugar-binding site. J Biol Chem 280:20712–20721

    Article  CAS  PubMed  Google Scholar 

  18. Das MK, Sharma RS, Mishra V (2011) A cytotoxic type-2 ribosome inactivating protein (from leafless mistletoe) lacking sugar binding activity. Int J Biol Macromol 49:1096–1103

    Article  CAS  PubMed  Google Scholar 

  19. Das MK, Sharma RS, Mishra V (2012) Induction of apoptosis by ribosome inactivating proteins. Appl Biochem Biotechnol 166:1552–1561

    Article  CAS  PubMed  Google Scholar 

  20. Shanavaskhan AE, Sivadasan M, Alfarhan AH, Thomas J (2012) Ethnomedicinal aspects of angiospermic epiphytes and parasites of Kerala, India. Indian J Tradit Knowl 11:250–258

    Google Scholar 

  21. Singh H, Krishna G, Baske PK (2010) Plants used in the treatment of joint diseases (rheumatism, arthritis, gout and lumbago) in Mayurbhanj district of Odisha, India. Rep Opin 2:22–26

    CAS  Google Scholar 

  22. Pradhan BK, Badola HK (2008) Ethnomedicinal plant use by Lepcha tribe of Dzongu valley, bordering Khangchendzonga biosphere reserve, in north Sikkim, India. J Ethnobiol Ethnomed 4:22

    Article  PubMed  PubMed Central  Google Scholar 

  23. Wiart C (2012) Medicinal plants of China, Korea, and Japan: bioresources for tomorrow’s drugs and cosmetics. Taylor & Francis, Boca Raton

    Book  Google Scholar 

  24. Liu Y (1986) Pharmaceutical composition for treating nonlymphatic leukemia and method of producing the same and its components. Chem Abstr 106:90200j

    Google Scholar 

  25. Bradford MM (1976) A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem 72:248–254

    Article  CAS  PubMed  Google Scholar 

  26. Vermes I, Haanen Steffens-Nakken H, Reutelingsperger C (1995) A novel assay for apoptosis flow cytometric detection of phosphatidylserine expression on early apoptotic cells using fluorescein labelled Annexin V. J Immunol Methods 184:39–51

    Article  CAS  PubMed  Google Scholar 

  27. Battelli MG, Citores L, Buonamici L, Ferreras JM, De Benito FM, Stirpe F, Girbés T (1997) Toxicity and cytotoxicity of nigrin b, a two-chain ribosome-inactivating protein from Sambucus nigra: comparison with ricin. Arch Toxicol 71:360–364

    Article  CAS  PubMed  Google Scholar 

  28. Ayyagari VN, Brard L (2014) Bithionol inhibits ovarian cancer cell growth in vitro-studies on mechanism(s) of action. BMC Cancer 14:61–77

    Article  PubMed  PubMed Central  Google Scholar 

  29. Ding X, Zhu FS, Li M, Gao SG (2012) Induction of apoptosis in human hepatoma SMMC-7721 cells by solamargine from Solanum nigrum L. J Ethnopharmacol 139:599–604

    Article  CAS  PubMed  Google Scholar 

  30. Gercel-Taylor C (2005) Diphenylamine assay of DNA fragmentation for chemosensitivity testing. Methods Mol Med 111:79–82

    CAS  PubMed  Google Scholar 

  31. Sikriwal D, Batra JK (2010) Ribosome inactivating proteins and apoptosis. Plant Cell Monogr 18:167–189

    Article  CAS  Google Scholar 

  32. Saxena N, Yadav P, Kumar O (2013) The Fas/Fas ligand apoptotic pathway is involved in abrin-induced apoptosis. Toxicol Sci 135:103–118

    Article  CAS  PubMed  Google Scholar 

  33. Bantel H, Engels IH, Voelter W, Klaus SO, Sebastian W (1999) Mistletoe lectin activates caspase-8/FLICE independently of death receptor signaling and enhances anticancer drug-induced apoptosis. Cancer Res 59:2083–2090

    CAS  PubMed  Google Scholar 

  34. Narayanan S, Surolia A, Karande A (2004) Ribosome-inactivating protein and apoptosis: abrin causes cell death via mitochondrial pathway in Jurkat cells. Biochem J 377:233–240

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  35. Elmore S (2007) Apoptosis: a review of programmed cell death. Toxicol Pathol 35:495–516

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  36. Hickman JA (1992) Apoptosis induced by anticancer drugs. Cancer Metastasis Rev 11:21–139

    Article  Google Scholar 

  37. Perl A, Gergely PJ, Nagy G, Koncz A, Banki K (2004) Mitochondrial hyperpolarization: a checkpoint of T-cell life, death and autoimmunity. Trends Immunol 25:360–367

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  38. Sánchez-Alcázar J, Ault J, Khodjakov A, Schneider E (2000) Increased mitochondrial cytochrome c levels and mitochondrial hyperpolarization precede camptothecin-induced apoptosis in Jurkat cells. Cell Death Differ 7:1090–1100

    Article  PubMed  Google Scholar 

  39. Scarlett JL, Sheard PW, Hughes G, Ledgerwood EC, Ku HH, Murphy MP (2000) Changes in mitochondrial membrane potential during staurosporine-induced apoptosis in Jurkat cells. FEBS Lett 475:267–272

    Article  CAS  PubMed  Google Scholar 

  40. Vander Heiden MG, Chandel NS, Li XX, Schumacker PT, Colombini M, Thompson CB (2000) Outer mitochondrial membrane permeability can regulate coupled respiration and cell survival. Proc Natl Acad Sci USA 97:4666–4671

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  41. Kim WH, Park WB, Gao B, Jung MH (2004) Critical role of reactive oxygen species and mitochondrial membrane potential in Korean mistletoe lectin-induced apoptosis in human hepatocarcinoma cells. Mol Pharmacol 66:1383–1396

    Article  CAS  PubMed  Google Scholar 

  42. Rao PVL, Jayaraj R, Bhaskar ASB, Kumar O, Bhattacharya R, Saxena P, Dash PK, Vijayaraghavan R (2005) Mechanism of ricin-induced apoptosis in human cervical cancer cells. Biochem Pharmacol 69:855–865

    Article  CAS  PubMed  Google Scholar 

  43. Aronis A, Melendez JA, Golan O, Shilo S, Dicter N, Tirosh O (2003) Potentiation of Fas-mediated apoptosis by attenuated production of mitochondria-derived reactive oxygen species. Cell Death Differ 10:335–344

    Article  CAS  PubMed  Google Scholar 

  44. Gulzeb A (2014) Procaspase-3 activating therapeutic agents in cancer therapy. Adv Pharm Ethanomed 2:1–6

    Article  Google Scholar 

  45. Lyu SY, Park WB, Choi KH, Kim WH (2001) Involvement of caspase-3 in apoptosis induced by Viscum album var. coloratum agglutinin in HL-60 cells. Biosci Biotechnol Biochem 65:534–541

    Article  CAS  PubMed  Google Scholar 

  46. Kim MS, So HS, Lee KM, Park JS, Lee JH, Moon SK, Ryu DG, Sy Chung, Jung BH, Kim YK, Moon G, Park R (2000) Activation of caspase cascades in Korean mistletoe (Viscum album var. coloratum) lectin-II-induced apoptosis of human myeloleukemic U937 cells. Gen Pharmacol Vasc Syst 34:349–355

    Article  CAS  Google Scholar 

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Acknowledgements

Authors thank the University of Delhi for Faculty research grant to VM, Miranda House for Flow Cytometer facility of the DS Kothari Centre for Research and Innovation in Science Education. RM thanks the University Grant Commission for JRF for Ph.D. and SS thanks the UGC for Non-NET Research Fellowship. Authors thank Professor Millind Sardesai for all support throughout the study.

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Correspondence to Vandana Mishra.

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Mishra, R., Das, M.K., Singh, S. et al. Articulatin-D induces apoptosis via activation of caspase-8 in acute T-cell leukemia cell line. Mol Cell Biochem 426, 87–99 (2017). https://doi.org/10.1007/s11010-016-2883-y

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