References

• 1. Siegel RL, Miller KD, Jemal A. Cancer statistics. Ca Cancer J Clin 2015; 65(1): 5-29. google scholar
• 2. Mobasheri A, Barrett-Jolley R. Aquaporin water channels in the mammary gland: From physiology to pathophysiology and neoplasia. J Mammary Gland Biol Neoplasia 2014;19(1): 91-102. google scholar
• 3. Harris HR, Bergkvist L, Wolk A. Adherence to the world cancer research fund/American Institute for Cancer Research recommendations and breast cancer risk. Int J Cancer 2016; 138(11): 2657-64. google scholar
• 4. Rillema JA. Development of the mammary gland and lactation. Trends Endocrinol Metab 1994; 5(4): 149-54. google scholar
• 5. Petanidis S, Kioseoglou E, Hadzopoulou-Cladaras M, Salifoglou A. Novel ternary vanadium-betaine-peroxido species suppresses H-ras and matrix metalloproteinase-2 expression by increasing reactive oxygen species-mediated apoptosis in cancer cells. Cancer Lett 2013; 335(2): 387-96. google scholar
• 6. Gruzewska K, Michno A, Pawelczyk T, Bielarczyk H. Essentiality and toxicity of vanadium supplements in health and pathology. J Physiol Pharmacol 2014; 65(5): 603-11. google scholar
• 7. Bishayee A, Waghray A, Patel MA, Chatterjee M. Vanadium in the detection, prevention and treatment of cancer: The in vivo evidence. Cancer Lett 2010; 294(1): 1-12. google scholar
• 8. Gonzalez-Villalva A, Pinon-Zarate G, De la Pena Diaz A, Flores-García M, Bizarro-Nevares P, Rendón-Huerta EP, et al. The effect of vanadium on platelet function. Environ Toxicol Pharmacol 2011; 32(3): 447-56. google scholar
• 9. Evangelou AM. Vanadium in cancer treatment. Critical Rev Oncol Hematol 2002; 42(3): 249-65. google scholar
• 10. Ekert PG, Vaux DL. Apoptosis and the immune system. Br Med Bulletin 1997; 53(3): 591-603. google scholar
• 11. Kostova I. Titanium and vanadium complexes as anticancer agents. Anticancer Agents Med Chem 2009; 9(8): 827-42. google scholar
• 12. Korbecki J, Baranowska-Bosiacka I, Gutowska I, Chlubek D. Biochemical and medical importance of vanadium compounds. Acta Biochim Pol 2012; 59(2): 195-200. google scholar
• 13. Liem DA, Gho CC, Gho BC, Kazim S, Manintveld OC, Verdouw PD, et al. The tyrosine phosphatase inhibitor bis(maltolato)-oxovanadium attenuates myocardial reperfusion injury by opening ATP-sensitive potassium channels. J Pharmacol Exp Ther 2004; 309(3): 1256-62. google scholar
• 14. Abakumova OY, Podobed OV, Belayeva NF, Tochilkin AI. Anticancer activity of oxovanadium compounds. Biomed Khim 2012; 6(2): 164-70. google scholar
• 15. Capella LS, Alcantara JS, Maura-Neto V, Lopes AG, Capella MA. Vanadate is toxic to adherent-growing multidrug-resistant cells. Tumor Biol 2000; 21(1): 54-62. google scholar
• 16. Suzuki T, Fujikura K, Higashiyama T, Takata K. DNA staining for fluorescence and laser confocal microscopy. J Histochem Cytochem 1997; 45(1): 49-53. google scholar
• 17. Canel M, Serrels A, Frame MC, Brunton VG. E-Cadherin-integrin crosstalk in cancer invasion and metastasis. J Cell Sci 2013; 126(Pt 2): 393-401. google scholar
• 18. Glauert AM, Lewis PR. Biological specimen preparation for transmission electron microscopy. Princeton University Press, New Jersey, 1998; ISBN: 0-691-00749-2 (Cloth), ISBN: 0-691-00900-7 (pbk). google scholar
• 19. Yamaguchi T, Watanabe S, Matsumura Y, Tokuoka Y, Yokoyama A. Oxovanadium complexes with quinoline and pyridinone ligands: Syntheses of the complexes and effect of alkyl chains on their apoptosis-inducing activity in leukemia cells. Bioorganic Med Chem 2012; 20(9): 3058-64. google scholar
• 20. Berx G, Van Roy F. Commentary: The E-cadherin/catenin complex: an important gatekeeper in breast cancer tumorigenesis and malignant progression. Breast Cancer Res 2001; 3(5): 289-93. google scholar
• 21. Holko P, Ligeza J, Kisielewska J, Kordowiak AM, Klein A. The effect of vanadyl sulphate (VOSO4) on autocrine growth on human epithelial cancer cell lines. Pol J Pathol 2008; 59(1): 3-8. google scholar
• 22. Tadakuma T, Kizaki H, Odaka C, Kubota R, Ishimura Y, Yagita H, et al. CD4+CD8+ thymocytes are susceptible to DNA fragmentation induced by phorbol ester, calcium ionophore and anti-CD3 antibody. Eur J Immunol 1990; 20(4): 779-84. google scholar
• 23. McConkey DJ, Hartzell P, Amador-Perez FJ, Orenius S, Jondal M. Calcium-dependent killing of immature thymocytes by stimulation via CD37T cell receptor complex. J Immunol 1989; 143(6): 1801-6. google scholar
• 24. Varecka L, Peterajova E, Sevcik J. Ca(2+)-activated K+ channel and the activation of Ca2+ influx in vanadate-treated red blood cells. Gen Physiol Biophys 1997; 16(4): 339-57. google scholar
• 25. Kordowiak AM, Klein A, Goc A, Dabroś W. Comparison of the effect of VOSO4, Na3VO4 and NaVO3 on proliferation, viability and morphology of H35-19 rat hepatoma cell line. Pol J Pathol 2007; 58(1): 51-7. google scholar
• 26. León IE, Cadavid Vargas JF, Tiscornia I, Porro V, Castelli S, Katkar P, et al. Oxidovanadium(IV) complexes with chrysin and silibinin: anticancer activity and mechanisms of action in a human colon adenocarcinoma model. J Biol Inorg Chem 2015; 20(7): 1175-91. google scholar
• 27. Umbas R, Schalken JA, Aalders TW, Carter BS, Karthaus HF, Schaafsma HE, et al. Expression of the cellular adhesion molecule E-cadherin is reduced or absent in high-grade prostate cancer. Cancer Res 1994; 52(18): 5104-09. google scholar
• 28. Oka H, Shiozaki H, Kobayashi K, Inoue M, Tahara H, Kobayashi T, et al. Expression of E-cadherin cell adhesion molecules in human breast cancer tissues and its relationship to metastasis. Cancer Research 1993; 53(7): 1696-01. google scholar
• 29. Molinuevo MS, Cortizo AM, Etcheverry SB. Vanadium (IV) complexes inhibit adhesion, migration and colony formation of UMR106 osteosarcoma cells. Cancer Chemother Pharmacol 2008; 61(5): 767-73. google scholar

Citations