The effects of L-NAME on DU145 human prostate cancer cell line: A cytotoxicity-based study

Kaçar S., Kar F., Hacioglu C., Kanbak G., Şahintürk V.

HUMAN & EXPERIMENTAL TOXICOLOGY, vol.39, no.2, pp.182-193, 2020 (SCI-Expanded) identifier identifier identifier

  • Publication Type: Article / Article
  • Volume: 39 Issue: 2
  • Publication Date: 2020
  • Doi Number: 10.1177/0960327119880591
  • Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus, Academic Search Premier, PASCAL, Agricultural & Environmental Science Database, BIOSIS, CAB Abstracts, Chimica, CINAHL, EMBASE, Environment Index, MEDLINE, Pollution Abstracts, Veterinary Science Database
  • Page Numbers: pp.182-193
  • Keywords: L-NAME, nitric oxide, DU145 prostate cancer cells, oxidative stress, inflammation, apoptosis, cell morphology, cytotoxicity, NITRIC-OXIDE SYNTHASE, OXIDATIVE STRESS, IN-VITRO, HYPERTENSION, PATHWAY, PROLIFERATION, INHIBITOR, CARCINOMA, APOPTOSIS, GROWTH
  • Kütahya Health Sciences University Affiliated: Yes


Of all cancer types, prostate cancer is the second most common one with an age-standardized incidence rate of 29.3 per 100,000 men worldwide. Nitric oxide (NO) is both a radical and versatile messenger molecule involved in many physiological activities. NO was documented to be highly secreted and utilized by cancer cells. N omega-nitro-l-arginine methyl ester (L-NAME) is utilized for inhibiting NO synthase. Its worst long-term side effect is reported to be hypertension, hence less cytotoxic than chemotherapeutic agents. Herein, we carried out a cytotoxicity study on how different doses of L-NAME affect DU145 human prostate cancer cells. First, toxic doses of L-NAME were determined. Then, while antioxidant capacity was determined by glutathione and total antioxidant status, oxidative stress was evaluated by quantifying malondialdehyde, NO, and total oxidant status levels. Inflammatory effects of L-NAME were investigated by measuring tumor necrosis factor-alpha and interleukin-6 (IL-6) levels. Apoptotic effects of L-NAME were evaluated by measuring cytochrome C somatic and caspase 3 levels and by staining Bax protein. Finally, morphological analysis was performed. IC50 of L-NAME against DU145 cells was 12.2 mM. In L-NAME-treated DU145 cells, a dose-dependent increase in oxidative stress, inflammatory, and apoptotic marker proteins and decrease in antioxidant capacity were observed. While at the moderate dose of L-NAME, apoptotic changes were commonly observed, at higher doses, vacuolated and swollen cells were also recorded. We believe that the present study will encourage future studies by providing insights about dose and effects of L-NAME.