DNA damage and repair in human lymphocytes and gastric mucosa cells exposed to chromium and curcumin

✍ Scribed by Janusz Błasiak; Andrzej Trzeciak; Ewa Małecka-Panas; Józef Drzewoski; Teresa Iwanienko; Irena Szumiel; Maria Wojewódzka

• Publisher: John Wiley and Sons
• Year: 1999
• Tongue: English
• Weight: 103 KB
• Volume: 19
• Category: Article
• ISSN: 0270-3211
• DOI: 10.1002/(sici)1520-6866(1999)19:1<19::aid-tcm3>3.0.co;2-h

✦ Synopsis

Human population can be considered as a subject of combined exposure to chemicals. Hexavalent chromium is a well-known mutagen and carcinogen. Curcumin, a popular spice and pigment, is reported to have antineoplastic properties. The single cell gel electrophoresis (Comet assay) is a sensitive technique that allows detecting double-and single-strand DNA breaks caused by a broad spectrum of mutagens. In the present work the ability of curcumin to reduce DNA damage induced by chromium in human lymphocytes and gastric mucosa (GM) cells was investigated by using the comet assay. Chromium at 500 mM evoked DNA damage measured as significant (P < 0.001), about a two-fold increase in comet tail moment of both lymphocytes and GM cells. Curcumin at 10, 25, and 50 mM also damaged DNA of both types of cells in a dose-dependent manner: the increase in the tail moment reached about twenty times of the control value (P < 0.001). The combined action of chromium at 500 mM and curcumin at 50 mM resulted in the significant (P < 0.001) increase in the comet tail moment of both types of cells. In each case, treated cells were able to recover within 60 min. Our study clearly demonstrates that curcumin does not inhibit DNA damaging action of hexavalent chromium in human lymphocytes and GM cells. Moreover, curcumin itself can damage DNA of these cells and the total effect of chromium and curcumin is additive. Further studies are needed to establish the role of interaction of curcumin with DNA in carcinogenesis.