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Effect of Botulinum Toxin A on Proliferation and Apoptosis in the T47D Breast Cancer Cell Line

  • Bandala, Cindy (Department of Research Support, Instituto Nacional de Rehabilitacion) ;
  • Perez-Santos, Jose Luis Martin (Vice-rectory of Research and Postgraduate Studies, Benemerita Universidad Autonoma de Puebla) ;
  • Lara-Padilla, Eleazar (Molecular Oncology and Oxidative Stress Laboratory, Escuela Superior de Medicina, Instituto Politecnico Nacional) ;
  • Delgado Lopez, Ma. Guadalupe (Laboratory of Cellular Biology, Centro de Investigacion Biomedica de Oriente, Instituto Mexicano del Seguro Social) ;
  • Anaya-Ruiz, Maricruz (Laboratory of Cellular Biology, Centro de Investigacion Biomedica de Oriente, Instituto Mexicano del Seguro Social)
  • Published : 2013.02.28

Abstract

The present study was performed to assess the activity of the botulinum toxin A on breast cancer cells. The T47D cell line was exposed to diverse concentrations of the botulinum toxin A and cell viability and apoptosis were estimated using MTT and propidium iodine/annexin V methods, respectively. Botulinum toxin A exerted greater cytotoxic activity in T47D cells in comparison with MCF10A normal cells; this appeared to be via apoptotic processes caspase-3 and -7. In conclusion, botulinum toxin A induces caspase-3 and -7 dependent apoptotic processes in the T47D breast cancer cell line.

Keywords

References

  1. Bray F, Ren JS, Masuyer E, Ferlay J (2013). Global estimates of cancer prevalence for 27 sites in adult population in 2008. Int J Cancer, 132, 1133-45. https://doi.org/10.1002/ijc.27711
  2. Edge SB (2013). Advances in breast surgery, 2002-2012. J Natl Compr Canc Netw. 11, 53-9.
  3. Gorgal T, Charrua A, Silva JF, et al (2012). Expression of apoptosis-regulating genes in the rat prostate following botulinum toxin type A injection. BMC Urol, 10, 12.
  4. Haghighat S, Akbari M, Ghaffari S (2012). Standardized breast cancer mortality rate compared to the general female population of Iran. Asian Pac J Cancer Prev, 13, 5525-8. https://doi.org/10.7314/APJCP.2012.13.11.5525
  5. Hamedeyazdan S, Fathiazad F, Sharifi S, Nazemiyeh H (2012). Antiproliferative activity of Marrubium persicum extract in the MCF-7 human breast cancer cell line. Asian Pac J Cancer Prev. 13, 5843-8. https://doi.org/10.7314/APJCP.2012.13.11.5843
  6. Hasegawa Y, Shimizu T, Takahashi N, Okada Y (2012). The apoptotic volume decrease is an upstream event of MAP kinase activation during staurosporine-induced apoptosis in HeLa cells. Int J Mol Sci, 13, 9363-79. https://doi.org/10.3390/ijms13079363
  7. Hassan ZK, Elamin MH, Daghestani MH, et al (2012). Oleuropein induces anti-metastatic effects in breast cancer. Asian Pac J Cancer Prev. 13, 4555-4559. https://doi.org/10.7314/APJCP.2012.13.9.4555
  8. Hassan ZK, Daghestani MH (2012). Curcumin effect on MMPs and TIMPs genes in a breast cancer cell line. Asian Pac J Cancer Prev, 13, 3259-64. https://doi.org/10.7314/APJCP.2012.13.7.3259
  9. Karsenty G, Rocha J, Chevalier S, et al (2009). Botulinum toxin type A inhibits the growth of LNCaP human prostate cancer cells in vitro and in vivo. Prostate, 69, 1143-50. https://doi.org/10.1002/pros.20958
  10. Kim SH, Park IH, Lee H, et al (2012). Efficacy of exemestane after nonsteroidal aromatase inhibitor use in metastatic breast cancer patients. Asian Pac J Cancer Prev, 13, 979-83. https://doi.org/10.7314/APJCP.2012.13.3.979
  11. Kominami K, Nakabayashi J, Nagai T, et al (2012). The molecular mechanism of apoptosis upon caspase-8 activation: quantitative experimental validation of a mathematical model. Biochim Biophys Acta, 1823, 1825-40. https://doi.org/10.1016/j.bbamcr.2012.07.003
  12. Lee NK, Shin KH, Park IH, Lee KS, Ro J (2012). Stage-to-stage comparison of neoadjuvant chemotherapy versus adjuvant chemotherapy in pathological lymph node positive breast cancer patients. Jpn J Clin Oncol, 42, 995-1001. https://doi.org/10.1093/jjco/hys130
  13. Mazo EB, Krivoborodov GG, Shkol'nikov ME, Efremov NS (2008). Botulinic toxin of type A in the treatment of prostatic adenoma and cancer. Urologia, 4, 63-6.
  14. Nam HJ, Kang JK, Chang JS, et al (2012). Cells transformed by PLC-gamma 1 overexpression are highly sensitive to clostridium difficile toxin A-induced apoptosis and mitotic inhibition. J Microbiol Biotechnol, 22, 50-7. https://doi.org/10.4014/jmb.1107.07018
  15. Proietti S, Nardicchi V, Porena M, Giannantoni A (2012). Botulinum toxin type-A toxin activity on prostate cancer cell lines. Urologia, 79, 135-41. https://doi.org/10.5301/RU.2012.9254
  16. Saraydin SU, Tuncer E, Tepe B, et al (2012). Antitumoral effects od Melissa officinalis on breast cancer in vitro and in vivo. Asian Pac J Cancer Prev, 13, 2765-70. https://doi.org/10.7314/APJCP.2012.13.6.2765
  17. Sendur MA, Aksoy S, Ozdemir NY, Zengin N, Altundag K (2012). What is the mechanism of progression with Trastuzumab treatment-escape or resistance? Asian Pac J Cancer Prev. 13, 5929-30. https://doi.org/10.7314/APJCP.2012.13.11.5915
  18. Smith RA, Duffy SW, Tabar L (2012). Breast cancer screening: the evolving evidence. Oncology. 26, 471-5.
  19. Tegenge MA, Bohnel H, Gessler F, Bicker G (2012). Beurotransmitter vesicle release from human model neurons (NT2) is sensistive to botulinum toxin A. Cell Mol Neurobiol, 32, 1021-9. https://doi.org/10.1007/s10571-012-9818-2
  20. Thirunavukkarasusx N, Ghosal KJ, Kukreja R, et al (2011). Microarray analysis of differentially regulated genes in human neuronal and epithelial cell lines upon exposure to type A botulinum neurotoxin. Biochem Biophys Res Commun, 405, 684-90. https://doi.org/10.1016/j.bbrc.2011.01.102
  21. Truin W, Voogd AC, Vreugdenhil G (2012). Effect of adjuvant chemotherapy in postmenopausal patients with invasive ductal versus lobular breast cancer. Ann Oncol. 23, 2859-65. https://doi.org/10.1093/annonc/mds180
  22. Yang L, Sun TT, Wang N (2012). The incidence and mortality trends of female breast cancer in Beijing, China: between 2004 and 2008. Zhonghua Yu Fang Yi Xue Za Zhi, 46, 1009-14.
  23. Yurinskaya VE, Moshkov AV, Wibberley AV (2012) Dual response of human leukemia U937 cells to hypertonic shrinkage: initial regulatory volume increase (RVI) and delayed apoptotic volume decrease (AVD). Cell Physiol Biochem, 30, 964-73. https://doi.org/10.1159/000341473
  24. Zhou SF, Shi WF, Meng D (2012). Interoperative radiotherapy of seventy-two cases of early breast cancer patients during breast-conserving surgery. Asian Pac J Cancer Prev, 13, 1131-5. https://doi.org/10.7314/APJCP.2012.13.4.1131

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