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Updated: Aug 9, 2026

The Lambda Select cII Mutation Detection System
Published on: April 26, 2018
A comparative study on the antimutagenicity of atorvastatin and lovastatin against directly acting mutagens
1Department of Biochemistry, Amala Institute of Medical Sciences, Amala Nagar, Thrissur, Kerala, India. taajith@rediffmail.com
Abstract:
Elevated levels of oxidative DNA lesions have been noted in many tumors and such damage is strongly implicated in the etiology of cancer. The cumulative risk of cancer increases with the fourth power of age and is associated with an accumulation of oxidative DNA damage. Many agents, synthetic or natural, that can inhibit mutation have been depicted as cancer chemopreventive agents. Antimutagenicity of the 3-hydroxy-3-methylgutaryl-CoA (HMG-CoA) reductase inhibitors atorvastatin and lovastatin was studied using the Ames Salmonella typhimurium assay. Directly acting mutagens, sodium azide (NaN(3)) and 4-nitro-o-phenylenediamine (NPDA), were used to induce mutation in Salmonella strains TA98 and TA100. The antimutagenicity of lovastatin and atorvastatin was found to be significant (p < 0.01) and dose-dependent. The percentage inhibition of a 3 mg lovastatin-treated plate was found to be 79.9% and 61.8% against NPDA- and NaN(3)-induced mutation to TA98 and TA100, respectively. Atorvastatin (0.5 mg/plate) inhibited NPDA-and NaN(3)-induced mutation to TA98 and TA100 by 78.6% and 45.5%, respectively. Atorvastatin showed antimutagenic activity at lower concentrations than lovatstatin. The results of the present study regarding the antimutagenic activity of atorvastatin and lovastatin suggested their therapeutic application as cancer chemopreventive agents.
Insights
Statins like atorvastatin and lovastatin show significant antimutagenic properties, inhibiting DNA damage linked to cancer. These findings suggest their potential as cancer chemopreventive agents, offering a new therapeutic avenue.
Area of Science:
- Biochemistry
- Genetics
- Pharmacology
Background:
- Oxidative DNA damage is a key factor in cancer development and progression.
- Cancer risk escalates significantly with age, correlating with accumulated DNA damage.
- Antimutagenic agents are explored for cancer chemoprevention.
Purpose of the Study:
- To investigate the antimutagenic potential of HMG-CoA reductase inhibitors, atorvastatin and lovastatin.
- To evaluate the efficacy of these statins in preventing DNA mutations induced by specific mutagens.
- To explore the therapeutic application of atorvastatin and lovastatin as cancer chemopreventive agents.
Main Methods:
- Utilized the Ames Salmonella typhimurium assay to assess antimutagenicity.
- Employed sodium azide (NaN(3)) and 4-nitro-o-phenylenediamine (NPDA) as direct-acting mutagens.
- Tested lovastatin and atorvastatin on Salmonella strains TA98 and TA100.
Main Results:
- Both lovastatin and atorvastatin demonstrated significant (p < 0.01) and dose-dependent antimutagenic activity.
- Lovastatin (3 mg) inhibited NPDA- and NaN(3)-induced mutations by 79.9% and 61.8%, respectively.
- Atorvastatin (0.5 mg) inhibited NPDA- and NaN(3)-induced mutations by 78.6% and 45.5%, respectively, showing activity at lower doses than lovastatin.
Conclusions:
- Atorvastatin and lovastatin possess significant antimutagenic properties.
- The study suggests a potential therapeutic role for these statins in cancer chemoprevention.
- Further research into statins as cancer chemopreventive agents is warranted.
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