Research on Biological Materials with Oxazinone Derivatives Induce Apoptosis in HT-29 Cells

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Abstract:

Objective: To monitor the induction of apoptosis in HT-29 cells by three compounds of oxazinone derivatives (A-C) with similar structures and research the mechanism of those oxazinone derivatives in induction of apoptosis in HT-29 cells. Methods: HT-29 cells were used for the determination of cytotoxicity elicited by oxazinone compounds. Cytotoxic effects of these compounds in HT-29 cells are monitored by a Real-Time Cell Analyser system. Results: All the oxazinone derivatives exhibited growth inhibition in HT-29 cells in a concentration-dependent manner. Conclusion: All the three compounds of oxazinone derivatives (A-C) could exhibit growth inhibition in HT-29 cells in a dose-dependent manner.

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220-223

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March 2014

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© 2014 Trans Tech Publications Ltd. All Rights Reserved

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[1] M. Malvezzi, P. Bertuccio, F. Levi, C. La Vecchia, E. Negri: Ann Oncol. 24(3) (2013), pp.792-800.

DOI: 10.1093/annonc/mdt010

Google Scholar

[2] L. Lang-Lazdunski: Eur Respir Rev. 22(129) (2013), pp.382-404.

Google Scholar

[3] J. Ho, B. Turkbey, M. Edgerly, M. Alimchandani, M. Quezado, K. Camphausen, T. Fojo, A. Kaushal: Role of radiotherapy in adrenocortical carcinoma. Cancer J. 19(4) (2013), pp.288-294.

DOI: 10.1097/ppo.0b013e31829e3221

Google Scholar

[4] A. Saadeddin: J Infect Public Health. 5 (2012), pp S45-49.

Google Scholar

[5] L. B. Saltz, S. Clarke, E. Díaz-Rubio, W. Scheithauer, A. Figer, R. Wong, S. Koski, M. Lichinitser, T. S. Yang, F. Rivera, F. Couture, F. Sirzén, J. Cassidy: J Clin Oncol. 26(12) (2008), p.2013-(2019).

DOI: 10.1200/jco.2007.14.9930

Google Scholar

[6] S. Dinner, R. Advani: J Natl Compr Canc Netw. 11(8) (2013), pp.968-976.

Google Scholar

[7] N. Li, X. Li, S. Huang, S. Shen, X. Wang: Zhong Nan Da Xue Xue Bao Yi Xue Ban. 38(8) (2013), pp.809-817.

Google Scholar

[8] L. L. Gunderson, J. M. Jessup, D. J. Sargent, F. L. Greene, A. K. Stewart: J Clin Oncol. 28(2) (2010), pp.264-271.

Google Scholar

[9] S. Aparo, S. Goel: Crit Rev Oncol Hematol. 83(1) (2012), pp.47-58.

Google Scholar

[10] A. S. Hossan, H. M. Abu-Melha, M. A. Al-Omar, Ael-G Amr: Molecules. 17(11) (2012), pp.13642-13655.

DOI: 10.3390/molecules171113642

Google Scholar

[11] M. A. Mesaik, S. Rahat, K. M. Khan, Zia-Ullah, M. I. Choudhary, S. Murad, Z. Ismail, Atta-ur-Rahman, A. Ahmad: 12(9) (2004), p.2049-(2057).

DOI: 10.1016/j.bmc.2004.02.034

Google Scholar

[12] J. M. Boyd, L. Huang, L. Xie, B. Moe, S. Gabos, X. F. Li: Anal Chim Acta. 615(1) (2008), pp.80-87.

Google Scholar

[13] J. Z. Xing, L. Zhu, S. Gabos, L. Xie: Toxicol In Vitro. 20(6)(2006), pp.995-1004.

Google Scholar

[14] X. He, J. Wang, J. Steele, X. Sun, W. Nie, S. Tzipori, H. Feng: J Microbiol Methods. 78(1) (2009), pp.97-100.

Google Scholar