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The Inhibitory Effect of Kerra TM , KS TM , and Minoza TM on Human Papillomavirus Infection and Cervical Cancer.

Kiattawee ChoowongkomonKhuanjarat ChoengpanyaChamsai PeintongTipaya EkalaksanananSulak TalawatPussadee SrathongJureeporn Chuerduangphui
Published in: Medicina (Kaunas, Lithuania) (2023)
Background and Objectives : Cervical cancer is one of the most common types of frequently found cancers in Thailand. One of the causative agents is the infection of the high-risk human papillomavirus (HPV) type 16 and 18. Traditional medicines are rich sources of bioactive compounds which are a valuable source for the development of novel cancer therapies. In this study, the therapeutic effects of 3 traditional medicines, Kerra TM , KS TM , and Minoza TM , were studied on HeLa and CaSki cells. Materials and Methods : The effects of Kerra TM , KS TM , and Minoza TM on cancer cells were evaluated through cytotoxicity and cell death assays. The infection assay using HPV-16 pseudovirus was also carried out. Results : All traditional medicines efficiently suppressed cell growths of HeLa and CaSki, with Kerra TM being the most potent anticancer agent followed by KS TM and Minoza TM . Kerra TM at 158 µg/mL and 261 µg/mL significantly increases the percentage inhibition of the HPV-16 pseudovirus infection in a pre-attachment step in a dose-dependent manner, while KS TM at 261 µg/mL efficiently inhibited viral infection in both pre-attachment and adsorption steps. However, Kerra TM , KS TM , and Minoza TM at subtoxic concentrations could not reduce the viral E6 mRNA expressions of HPV-16 and HPV-18. Cell death assay by acridine orange/ethidium bromide showed that Kerra TM increased population of dead cells in dose-dependent manner in both CaSki and HeLa. The percentage of secondary necrosis in Kerra TM -treated CaSki was higher than that of HeLa cells, while the percentage of late apoptotic cells in HeLa was higher than that of CaSki, indicating that HeLa was more susceptible to Kerra TM than CaSki. For KS TM and Minoza TM , these extracts at 250 µg/mL promoted autophagy over cell death. At 500 µg/mL, the percentage of dead cells in Kerra TM was higher than that of KS TM and Minoza TM . Conclusions : Kerra TM is a potent traditional medicine for promoting cancer cell death. Kerra TM is possibly useful in the prevention and treatment of cervical cancer. Further investigation will be carried out to gain a better understanding of the biochemical mechanism and the pharmacological activity underlying this effect.
Keyphrases
  • cell death
  • cell cycle arrest
  • induced apoptosis
  • squamous cell carcinoma
  • high grade
  • stem cells
  • oxidative stress
  • cell proliferation
  • high throughput
  • endoplasmic reticulum stress
  • newly diagnosed
  • binding protein