THE EFFECT OF LASER IRRADIATION ON THE VIABILITY OF HUMAN BREAST CANCER CELL, MDA-MB-231

Authors

  • Aishah Badruzzaman Physics Department, Faculty of Science, 81310 UTM Johor, Malaysia
  • Noriah Bidin Laser Center, Ibnu Sina Institute for Scientific & Industrial Research, Universiti Teknologi Malaysia, 81310 UTM Johor Bahru, Johor, Malaysia.
  • Siti Pauliena Mohd Bohari Faculty of Bioscience and Medical Engineering, Universiti Teknologi Malaysia, 81310 UTM Johor Bahru, Johor, Malaysia

DOI:

https://doi.org/10.11113/jt.v78.7548

Keywords:

Photothermal laser, MDA-MB-231, Excimer, postmastectomy lymphedema

Abstract

This study compared the effects of different sources of laser phototherapy on the cell viability of the in vitro human breast cancer cell lines. Laser phototherapy is used in the breast cancer clinical treatment, despite the limited safety information of laser irradiation effect on the cancer cell behavior. This study contributed on the development of guidelines for safer laser usage in treating breast cancer and minimising the possibility of activating postmastectomy lymphedema. Cancer cell viability and morphology were studied in this research. Human breast cancer (MDA-MB-231) cell lines were cultured for 24 hours in CO2 incubator and irradiated with different laser sources and number of pulse. The viability of cancer cells were assessed by MTT assay 24 hours after laser irradiation. The result showed that MDA-MB-231 cell viability increased after being irradiated by excimer 248 nm laser. However, the cancer cell viability slightly decreased after irradiation by both Nd:YAG 1064 and 532 nm. Although certain doses of laser may affect the MDA-MB-231 cell viability, additional laser exposures had nearly no effect. The research shows that Nd:YAG 1064 nm more effective in lowering cancer cell survivability than 532 nm and 248 nm. Further in vivo studies are needed for better understanding on the mechanism of laser-tissue interaction and improve the laser usage safety in photothermal therapy. 

References

Rubinov, A. N. 2003. Physical Grounds For Biological Effect Of Laserradiation. J. Physics D: Appl. Physics. 36: 2317-2330.

Hawkins, D. H., Tech, M. Abrahamse, H. 2006. The Role Of Laser Fluence In Cell Viability, Proliferation, And Membrane Integrity Of Wounded Human Skin Fibroblasts Following Helium-Neon Laser Irradiation. Laser Surg. Med. 38: 74-83.

Carati, C. J., Anderson, S. N., Gannon, B. J. and Piller, N.B. 2003. Treatment Of Postmastectomy Lymphedema With Low-Level Laser Therapy: A Double Blind, Placebo-Controlled Trial. Cancer. 98: 1114-1122.

Gur, A., Cosut, A., Sarac, A. J., Cevik, R., Nas, K. Uyar, A. 2003. Efficacy Of Different Therapy Regimes Of Low-Power Laser In Painful Osteoarthritis Of The Knee: A Double-Blind And Randomized-Controlled Trial. Laser Surg. Med. 33: 330-338.

Hopkins, J. T., McLoda, T. A., Seegmiller, J. G. and Baxter, G. D. 2004. Low-Level Laser Therapy Facilitates Superficial Wound Healing In Humans: A Triple-Blind, Sham-Controlled Study. J. Athl. Training. 39: 223-229.

Carati, C. J., Gannon, B. J. and Piller, N. B. 2004. Low-Level Laser As A Treatment Option For Postmastectomy Lymphedema. Am. J. Oncol. 3: 2-7.

Oliver, G. and Detmar, M. 2002. The Rediscovery Of The Lymphatic System: Old And New Insights Into The Development And Biological Function Of The Lymphatic Vasculature. Genes Dev. 16: 773-783.

Kaviani, A., Fateh, M., Nooraie, R. Y., Alinagi-Zadeh, M. Ataie-Fashtami, L. 2006. Low-Level Laser Therapy In Management Of Postmastectomy Lymphedema. Laser Med. Sci. 21: 90-94.

Hayes, S., Cornish, B. Newman, B. 2006. Prevalence And Cumulative Burden Of Lymphoedema Between 6 To 18 Months Following Treatment For Breast Cancer In Brisbane Women. 6th Australasian Lymphology Association Conference. 106-110.

Casley-Smith, J. 1992. Modern Treatment Of Lymphoedema. I. Complex Physical Therapy: The First 200 Australian Limbs. Australasian Journal of Dermatology. 33(2): 61-8.

Harris, S. R., Hugi, M. R., Olivotto, I. A., Levine, M. 2001. Clinical Practice Guidelines For The Care And Treatment Of Breast Cancer: 11. Lymphedema. Canadian Medical Association Journal. 23: 164(2): 191-9.

Rodrick, J. R., Poage, E., Wanchai, A., Stewart, B. R., Cormier, J. N., Armer, J. M. 2013. Complementary, Alternative, And Other Non-Complete Decongestive Therapy (CDT) Treatment Methods In The Management Of Lymphedema. A Systematic Search And Review. American Academy of Physical Medicine and Rehabilitation. 6: 250-274.

Carati, C. J., Anderson, S. N., Gannon, B. J., Piller, N. B. 2003. Treatment Of Postmastectomy Lymphedema With Low-Level Laser Therapy. A Double Blind, Placebo-Controlled Trial. Cancer. 98(6): 1114-1122.

Ahmed Omar, M. T., Abd-El-GayedEbid, A., El Morsy, A.M. 2011. Treatment Of Postmastectomy Lymphedema With Laser Therapy: Double Blind Placebo Control Randomized Study, Journal of Surgical Research. 165: 82-90.

Kozanoglu, E., Basaran, S., Paydas, S., Sarpel, T. 2009. Efficacy Of Pneumatic Compression And Low-Level Laser Therapy In The Treatment Of Postmastectomylymphoedema: A Randomized Controlled Trial. Clinical Rehabilitation. 23(2): 117-124.

Zainuddina, Traian, V., Chirilaa, Zeke Barnarda, Gregory S., Watsonf, ChiongTohc, IdrissBlakeyc, Andrew K. Whittakera, David J. T., Hill. 2011. F2 Excimer Laser (157 nm) Radiation Modification And Surface Ablation Of PHEMA Hydrogels And The Effects On Bioactivity: Surface Attachment And Proliferation Of Human Corneal Epithelial Cells Radiation. Physics and Chemistry. 80(2): 219-229

Richard W. Darrell, Ronald R. Krueger, Stephen L. Trokel. 1985. Excimer Laser Therapy for Experimental Candida Keratitis Olivia Serdarevic. American Journal of Ophthalmology. 99(5): 534-538

Powell, K., Low, P., McDonnell, P. A., Laakso, E. L., Ralph, S. J. 2010. The Effect Of Laser Irradiation On Proliferation Of Human Breast Carcinoma, Melanoma, And Immortalized Mammary Epithelial Cells. Photomedicine And Laser Surgery. 28(1): 115-123.

Schartinger, V. H., Galvan, O., Riechelmann, H., Dudás, J. 2012. Differential Responses Of Fibroblasts, Non- Neoplastic Epithelial Cells, And Oral Carcinoma Cells To Low Level Laser Therapy. Support Care Cancer. 20(3): 523-529.

Gao, X., Chen, T., Xing, D., Wang, F., Pei, Y., Wei, X. 2006. Single Cell Analysis Of PKC Activation During Proliferation And Apoptosis Induced By Laser Irradiation. Journal of Cellular Physiology. 206(2): 441-448.

Mikhailov, V. A., Denisov, I. N., Frank, G. A. and Voltchenko, N. N. 2000. Results Of Treatment Of Patients With Second- To Third-Stage Breast Cancer By Combination Of Low-Level Laser Therapy (LLLT) And Surgery: Ten-Year Experience. Proc. Soc. Photo. Opt. Instrum. Eng. 4166: 40.

Lenhard, R. E., Osteen, R. T., and Gansler, T. 2001. Clinical Oncology. Atlanta GA. The American Cancer Society. 25-30.

Werneck, C. E., Pinheiro, A. L. B., Pacheco, M. T. T., Soares, C. P., and De Castro, J. L. F. 2005. Laser Light Is Capable Of Inducing Proliferation Of Carcinoma Cells In Culture: A Spectroscopic In Vitro Study. Photomedicine and Laser Surgery. 23: 300-303.

Halsted W. 1894. The Results Of Operations For The Cure Of Cancer Of The Breast Performed At The Johns Hopkins Hospital From June, 1889 To January, 1894. Ann Surg. 20(5): 497-555.

Silvia, E. M., Lilian, V. R., Mônica F. F., Angélica, R. A., Camila, T. V. 2014. Treatment Of Upper Limb Lymphedema With Low-Level Laser: A Systematic Review. FisioterapiaemMovimento. 27(4): 663-74

Karu T. I .1987. Photobiological Fundamentals Of Low-Power Laser Therapy. IEEE J Quantum Electron. 23(10): 1703-17.

Welch, Jorge, A. J., Torres, H., Wai-Fung Cheong. (1989). Laser Physics and Laser-Tissue Interaction. Texas Heart Institute Journal. 16(14): 1-9.

Harris, S. R., Hugi, M. R., Olivotto, I. A. Levine, M. 2001. Clinical Practice Guidelines For The Care And Treatment Of Breast Cancer: 11. Lymphedema. Can. Med. Assoc. J. 164: 191-199.

Mgbonyebi, O. P., Russo, J., Russo, I. H. 1999. Roscovitine Induces Cell Death And Morphological Changes Indicative Of Apoptosis In MDA-MB-231 Breast Cancer Cells. Cancer Research. 59(8): 1903-10.

Serge, H., Yves, L., Marc, P. 2000. Oleate Activates Phosphatidylinositol 3-Kinase and Promotes Proliferation and Reduces Apoptosis of MDA-MB-231 Breast Cancer Cells, Whereas Palmitate Has Opposite Effects. Cancer Research. 60: 6353– 6358.

Keiko, T., George, L. 2004. Disruption Of Mitochondria During Tocotrienol-Induced Apoptosis In MDA-MB-231 Human Breast Cancer Cells. Biochemical Pharmacology. 67: 315-324.

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Published

2016-02-21

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Section

Science and Engineering

How to Cite

THE EFFECT OF LASER IRRADIATION ON THE VIABILITY OF HUMAN BREAST CANCER CELL, MDA-MB-231. (2016). Jurnal Teknologi, 78(3). https://doi.org/10.11113/jt.v78.7548