In vitro antiproliferative cytotoxic activity of 2 3 biindole againstvarious cancer cell lines     
Yazarlar (4)
Salih Ökten
Kırıkkale Üniversitesi, Türkiye
Prof. Dr. Ramazan ERENLER Tokat Gaziosmanpaşa Üniversitesi, Türkiye
Tuğba Kul Köprülü
Tokat Gaziosmanpaşa Üniversitesi, Türkiye
Şaban Tekin
Tokat Gaziosmanpaşa Üniversitesi, Türkiye
Makale Türü Özgün Makale
Makale Alt Türü SSCI, AHCI, SCI, SCI-Exp dergilerinde yayınlanan tam makale
Dergi Adı Turkish Journal of Biology
Dergi ISSN 1300-0152 Wos Dergi Scopus Dergi
Dergi Tarandığı Indeksler SCI-Expanded
Dergi Grubu Q4
Makale Dili İngilizce
Basım Tarihi 01-2015
Cilt No 39
Sayı 1
Sayfalar 15 / 22
DOI Numarası 10.3906/biy-1402-60
Makale Linki http://online.journals.tubitak.gov.tr/openDoiPdf.htm?mKodu=biy-1402-60
Özet
2,3\\\'-Biindole (2) was synthesized via bromination of indole (1) with molecular bromine and underwent simultaneous dimerization. Antiproliferative and cytotoxic activity of 2 was investigated in vitro on C6 (rat brain tumor), HeLa (human cervix carcinoma), and HT29 (human colon carcinoma) cells lines by using BrdU cell proliferation ELISA and lactate dehydrogenase (LDH) assays. In contrast to 5-fluorouracil (5-FU), 2,3\\\'-biindole (2) significantly inhibited proliferation of HeLa and HT29 cell lines. According to LDH assay, the cytotoxicity of compound 2 was low on HT29 cell lines and high on HeLa and C6 cell lines. Moreover, 2 did not cause any DNA laddering on the DNA of tested cells; therefore, it is suggested that the mechanism of action of this compound may not involve apoptosis. In addition, 2 inhibited relaxation of supercoiled plasmid DNA by topoisomerase activity. Results of the present study indicates that biindole (2) may have promising anticancer and antitopoisomerase potential with an unknown mechanism of action.
Anahtar Kelimeler
2,3 '-Biindole | anticancer | cytotoxicity | apoptosis | antitopoisomerase | C6 cell line | HeLa cell line | HT29 cell line
BM Sürdürülebilir Kalkınma Amaçları
Atıf Sayıları
WoS 15
TRDizin 2
In vitro antiproliferative cytotoxic activity of 2 3 biindole againstvarious cancer cell lines

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