Diallyl disulfide enhances carbon ion beams-induced apoptotic cell death in cervical cancer cells through regulating Tap73 /ΔNp73

Cell Cycle. 2015;14(23):3725-33. doi: 10.1080/15384101.2015.1104438.

Abstract

Diallyl disulfide (DADS), extracted from crushed garlic by steam-distillation, has been reported to provide the anticancer activity in several cancer types. However, the effect of DADS on high-LET carbon beams - induced cell death remains unknown. Therefore, we used human cervical cancer cells to elucidate the molecular effects of this diallyl sulfide. Radiotherapy remains the mainstay of treatment, especially in advanced cervical cancer and there is still space to improve the radiosensitivity to reduce radiation dosage. In this study, we found that radiation effects evoked by high-LET carbon beam was marked by inhibition of cell viability, cell cycle arrest, significant rise of apoptotic cells, regulation of transcription factor, such as p73, as well as alterations of crucial mediator of the apoptosis pathway. We further demonstrated that pretreatment of 10 µM DADS in HeLa cells exposed to radiation resulted in decrease in cell viability and increased radiosensitivity. Additionally, cells pretreated with DADS obviously inhibited the radiation-induced G2/M phase arrest, but promoted radiation-induced apoptosis. Moreover, combination DADS and the radiation exacerbated the activation of apoptosis pathways through up-regulated ration of pro-apoptotic Tap73 to anti-apoptotic ΔNp73, and its downstream proteins, such as FASLG, and APAF1. Taken together, these results suggest that DADS is a potential candidate as radio sensitive agent for cervical cancer.

Keywords: Diallyl disulfide; Tap73; apoptosis; cervical carcinoma; high-LET carbon beam; radiosensitivity; ΔNp73.

MeSH terms

  • Allyl Compounds / pharmacology*
  • Apoptosis / drug effects*
  • Apoptosis / radiation effects
  • Cell Cycle Checkpoints / drug effects
  • Cell Cycle Checkpoints / radiation effects
  • DNA-Binding Proteins / genetics*
  • Disulfides / pharmacology*
  • Female
  • Gene Expression / drug effects
  • Gene Expression / radiation effects
  • HeLa Cells
  • Heavy Ion Radiotherapy*
  • Humans
  • Nuclear Proteins / genetics*
  • Tumor Protein p73
  • Tumor Suppressor Proteins / genetics*
  • Uterine Cervical Neoplasms / drug therapy
  • Uterine Cervical Neoplasms / radiotherapy*

Substances

  • Allyl Compounds
  • DNA-Binding Proteins
  • Disulfides
  • Nuclear Proteins
  • TP73 protein, human
  • Tumor Protein p73
  • Tumor Suppressor Proteins
  • delta Np73 protein, human
  • diallyl disulfide

Grants and funding

This work was supported by grants from the Key Program of National Natural Science Foundation of China (U1432248), National Natural Science Foundation of China (No. 11175222; No. 11205219) , and the Western Talent Program of Chinese Academy of Sciences (Y260230XB0).