Contribution of Nitric Oxide and Epidermal Growth Factor Receptor in Anti-Metastatic Potential of Paclitaxel in Human Liver Cancer Cell (HebG2)‎

Abstract EN

Background : Paclitaxel is a general antineoplastic drug used against different types of experimental and human tumors.

Several anti-cancer drugs have been shown to stimulate nitric oxide (NO) production, which has been shown to affect many aspects of tumor biology.

Objective : This study was initiated to determine if paclitaxel stimulates NO production in HebG2 cells, and if so, whether NO interferes with the metastatic potential of HebG2 cells and contributes to paclitaxel cytotoxicity.

In addition, we sought to determine the relationship between NO production and the expression of epidermal growth factor receptor (EGFR) and matrix metaloproteinases (MMPs) in HebG2 cells.

Materials and Methods : The effects of paclitaxel (0.1-1000nM) on surviving fraction, NO production and the expression of EGFR, MMP-2 and MMP-9 were studied in human liver cancer cells (HebG2).

Results : Paclitaxel resulted in a significant dosedependent decrease in the surviving fraction of HebG2 cells.

A 62 % and 86 % decrease in the surviving fraction was attained at 10nM and 100nM paclitaxel, respectively.

Paclitaxel produced a significant increase in NO production, starting from 1nM.

A 64 % and 111 % increase in NO production was attained after exposure to 10nM and 100 nM of paclitaxel, respectively.

In all of the HebG2 cells treated with paclitaxel (1.0-1000nM) mRNA specific for EGFR, MMP-2 and MMP-9 were undetectable.

However, untreated HebG2 cells and those treated with paclitaxel (0.1nM) expressed mRNA specific for these markers.

Conclusion : This study suggests that : (1) increased production of NO may contribute to paclitaxel’s cytotoxicity against HebG2 cells, (2) paclitaxel may inhibit tumor metastasis via inhibition of the expression of EGFR and MMPs and (3) an inverse correlation exisits between NO production and expression of EGFR and MMPs.