Lobarstin enhances chemosensitivity in human glioblastoma T98G cells.

Abstract:

BACKGROUND/AIM:Lobarstin is a metabolite occurring from the Antarctic lichen Stereocaulon alpnum. Human glioblastoma is highly resistant to chemotherapy with temozolomide. Lobarstin was examined for its effect on glioblastoma. MATERIALS AND METHODS:Temozolomide-resistant T98G cells were subjected to toxicity test with temozolomide and/or lobarstin. DNA damage and recovery was assessed by the alkaline comet assay and expression of DNA repair genes was examined by RT-PCR and western blot analysis. RESULTS:Lobarstin alone at 40 μM was toxic against T98G, but had no effect in primary human fibroblasts. Co-treatment of lobarstin with temozolomide yielded enhanced toxicity. Temozolomide-alone or with lobarstin co-treatment gave similar extent of DNA damage. However, the recovery was reduced in co-treated cells. Expression of DNA repair genes, O(6)-methylguanine-DNA methyltransferase, poly(ADP-ribose) polymerase 1 and ligase 3 were reduced in lobarstin-treated cells. CONCLUSION:Enhanced sensitivity to temozolomide by lobarstin co-treatment may be attributed to reduced DNA repair.

journal_name

Anticancer Res

journal_title

Anticancer research

authors

Kim S,Jo S,Lee H,Kim TU,Kim IC,Yim JH,Chung H

subject

Has Abstract

pub_date

2013-12-01 00:00:00

pages

5445-51

issue

12

eissn

0250-7005

issn

1791-7530

pii

33/12/5445

journal_volume

33

pub_type

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