Abstract

To analyze the effects of a new unknown peptide DEF on the growth of tumor cells, a fused polypeptide TAT-DV1-DEF was designed and synthesized. The lung adenocarcinoma cell line GLC-82 treated with TAT- DV1-DEF was analyzed with a cell counting kit 8, and the location of polypeptides in cells was observed under laser confocal microscopy. The efficiency of polypeptide transfection and changes in nuclear morphology were analyzed by flow cytometry and fluorescence microscopy, respectively. Finally, the mechanism of tumor cell growth inhibition was evaluated by Western blotting. We found that TAT-DV1-DEF could significantly inhibit the growth of the lung adenocarcinoma cell line GLC-82, but not the normal human embryonic kidney cell line HEK-293. Polypeptides were found to be mostly localized in the cytoplasm and some mitochondria. The efficiency of polypeptide transfection in the two cell types was approximately 99%. Apoptotic nuclei were observed under fluorescence microscopy upon treatment with polypeptides and DAPI staining. Western blot analyses indicated that the polypeptide inhibition of tumor cell growth was apoptosis dependent. In the present study, we demonstrated that fused polypeptides could induce apoptosis of the lung adenocarcinoma cell line GLC-82, indicating that the new unknown peptide DEF has antitumor effects.

Highlights

  • Apoptosis is a very important procedure in eukaryotic development and cell homeostasis

  • The lung adenocarcinoma cell line GLC-82 treated with TATDV1-DEF was analyzed with a cell counting kit 8, and the location of polypeptides in cells was observed under laser confocal microscopy

  • We found that transcription protein (TAT)-DV1-DEF could significantly inhibit the growth of the lung adenocarcinoma cell line GLC-82, but not the normal human embryonic kidney cell line HEK-293

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Summary

Introduction

Apoptosis is a very important procedure in eukaryotic development and cell homeostasis. During the past 30 years, there have been many studies on the efficacy of apoptosis as a potential target for cancer therapy and the mechanism by which the failure of tumor cells to undergo apoptosis leads to malignant potential and chemotherapeutic resistance (Huerta et al, 2006). Available treatments for lung cancer are problematic, and there is a pressing need to develop appropriate treatments that are effective and have fewer side effects. This need has led to research on lung cancer treatments that target specific cellular signaling pathway proteins associated with tumors (Movassaghian et al, 2013)

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