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Piperlongumine Induces Apoptosis in Colorectal Cancer HCT 116 Cells Independent of Bax, p21 and p53 Status.
DA Silva Machado, Fernanda; Munari, Fernanda Mosena; Scariot, Fernando Joel; Echeverrigaray, Sergio; Aguzzoli, Cesar; Pich, Claus Tröger; Kato, Massuo Jorge; Yamaguchi, Lydia; Moura, Sidnei; Henriques, João Antonio Pêgas; Roesch-Ely, Mariana.
Affiliation
  • DA Silva Machado F; Laboratory of Genomics, Proteomics and DNA Repair, Biotechnology Institute, University of Caxias do Sul, Caxias do Sul, Brazil.
  • Munari FM; Laboratory of Genomics, Proteomics and DNA Repair, Biotechnology Institute, University of Caxias do Sul, Caxias do Sul, Brazil.
  • Scariot FJ; Laboratory of Genomics, Proteomics and DNA Repair, Biotechnology Institute, University of Caxias do Sul, Caxias do Sul, Brazil.
  • Echeverrigaray S; Laboratory of Genomics, Proteomics and DNA Repair, Biotechnology Institute, University of Caxias do Sul, Caxias do Sul, Brazil.
  • Aguzzoli C; Laboratory of Genomics, Proteomics and DNA Repair, Biotechnology Institute, University of Caxias do Sul, Caxias do Sul, Brazil.
  • Pich CT; Laboratory of Genomics, Proteomics and DNA Repair, Biotechnology Institute, University of Caxias do Sul, Caxias do Sul, Brazil.
  • Kato MJ; Laboratory of Genomics, Proteomics and DNA Repair, Biotechnology Institute, University of Caxias do Sul, Caxias do Sul, Brazil.
  • Yamaguchi L; Laboratory of Genomics, Proteomics and DNA Repair, Biotechnology Institute, University of Caxias do Sul, Caxias do Sul, Brazil.
  • Moura S; Laboratory of Genomics, Proteomics and DNA Repair, Biotechnology Institute, University of Caxias do Sul, Caxias do Sul, Brazil.
  • Henriques JAP; Laboratory of Genomics, Proteomics and DNA Repair, Biotechnology Institute, University of Caxias do Sul, Caxias do Sul, Brazil.
  • Roesch-Ely M; Laboratory of Genomics, Proteomics and DNA Repair, Biotechnology Institute, University of Caxias do Sul, Caxias do Sul, Brazil mrely@ucs.br.
Anticancer Res ; 38(11): 6231-6236, 2018 Nov.
Article in En | MEDLINE | ID: mdl-30396942
BACKGROUND/AIM: Colorectal cancer is a common type of cancer with reported resistance to treatment, in most cases due to loss of function of apoptotic and cell-cycle proteins. Piperlongumine (PPLGM) is a natural alkaloid isolated from Piper species, with promising anti-cancer properties. This study investigated whether PPLGM is able to induce cell death in colorectal carcinoma HCT 116 cells expressing wild-type or deficient in Bax, p21 or p53. MATERIALS AND METHODS: PPLGM was extracted from roots of Piper tuberculatum. Cell viability was determined by reduction of 3-(4,5-dimethilthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) and clonogenic assay. Cell death was evaluated by acridine orange/ethidium bromide staining and flow cytometry. Plasmid cleavage activity and circular dichroism DNA interaction were also analyzed. RESULTS: PPLGM induced selective cell death in all cell lines (IC50 range from 10.7 to 13.9 µM) with an increase in the number of late apoptotic cells and different profiles in cell-cycle distribution. Plasmid DNA analysis showed that PPLGM does not interact directly with DNA. CONCLUSION: This paper suggests that PPLGM may be a promising candidate in colorectal cancer therapy.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Colorectal Neoplasms / Tumor Suppressor Protein p53 / Dioxolanes / Bcl-2-Associated X Protein / Cyclin-Dependent Kinase Inhibitor p21 Limits: Humans Language: En Journal: Anticancer Res Year: 2018 Document type: Article Affiliation country: Brazil Country of publication: Greece

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Colorectal Neoplasms / Tumor Suppressor Protein p53 / Dioxolanes / Bcl-2-Associated X Protein / Cyclin-Dependent Kinase Inhibitor p21 Limits: Humans Language: En Journal: Anticancer Res Year: 2018 Document type: Article Affiliation country: Brazil Country of publication: Greece