1. Academic Validation
  2. Anthracene-9, 10-dione derivatives induced apoptosis in human cervical cancer cell line (CaSki) by interfering with HPV E6 expression

Anthracene-9, 10-dione derivatives induced apoptosis in human cervical cancer cell line (CaSki) by interfering with HPV E6 expression

  • Eur J Med Chem. 2014 Apr 22:77:334-42. doi: 10.1016/j.ejmech.2014.02.006.
Supranee Sangthong 1 Naunpun Sangphech 2 Tanapat Palaga 3 Nattaya Ngamrojanavanich 4 Songchan Puthong 5 Tirayut Vilaivan 6 Nongnuj Muangsin 7
Affiliations

Affiliations

  • 1 Program of Biotechnology, Faculty of Science, Chulalongkorn University, Bangkok 10330, Thailand.
  • 2 Medical Microbiology Interdisciplinary Program, Graduate School, Chulalongkorn University, Payathai Road, Pathumwan, Bangkok 10330, Thailand.
  • 3 Department of Microbiology, Faculty of Science, Chulalongkorn University, 254 Phayathai Road, Phatumwan, Bangkok 10330, Thailand. Electronic address: Tanapat.p@chula.ac.th.
  • 4 Biomaterials and Bioorganic Chemistry Research Group, Department of Chemistry, Faculty of Science, Chulalongkorn University, 254 Phayathai Road, Phatumwan, Bangkok 10330, Thailand.
  • 5 The Institute of Biotechnology and Genetic Engineering, Chulalongkorn University, 254 Phayathai Road, Bangkok 10330, Thailand.
  • 6 Department of Chemistry, Chulalongkorn University, 254 Phayathai Road, Bangkok 10330, Thailand.
  • 7 Biomaterials and Bioorganic Chemistry Research Group, Department of Chemistry, Faculty of Science, Chulalongkorn University, 254 Phayathai Road, Phatumwan, Bangkok 10330, Thailand. Electronic address: Nongnuj.j@chula.ac.th.
Abstract

A new series of anthracene-9, 10-dione derivatives have been synthesized to increase cytotoxic activity against human papillomavirus (HPV) positive Cancer cell line, CaSki. The highest cytotoxicity was achieved by 4-(benzylamino)-9,10-dioxo-4a,9,9a,10-tetrahydroanthracen-1-yl 4-ethylbenzenesulfonate (5) with the inhibitory concentration 50 (IC50) of 0.3 μM which is 20 times lower than that of cisplatin (CDDP; IC50 = 8.0 μM). The toxicity against non-cancerous cell line, WI-38, was low with the IC50 > 10 μM. Treatment with this compound resulted in decreasing HPV E6 expression. Furthermore, increasing p53 and decreasing Bcl-2 expression were noted. Cell cycle profiles revealed an accumulation of cells in the G2/M phase.

Keywords

10-Dione; Anthracene-9; Apoptosis; Cell cycle; Cervical cancer; HPV E6; p53.

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