Resnick Lionel, Rabinovitz Harold, Binninger David, Marchetti Maria, Weissbach Herbert
Center for Molecular Biology and Biotechnology, Florida Atlantic University, Boca Raton, FL 33431, USA.
J Drugs Dermatol. 2009 Jan;8(1):29-32.
Actinic keratoses (AKs) are a precancerous condition of the skin that have the potential to become squamous cell cancer (SCC). Sulindac is a Food and Drug Administration (FDA)-approved nonsteroidal anti-inflammatory drug (NSAID) that has been shown to have clinically significant anticancer effects. Malignant cells may have a different response to oxidative stress than normal cells.
To establish a role of increased reactive oxygen species (ROS) in the mechanism of cancer killing by sulindac in the presence of an oxidizing agent. To assess the tolerability and efficacy of the combination of gels containing sulindac and hydrogen peroxide in the treatment of patients with AKs.
Cell culture studies were performed using a skin SCC cell line and normal human epidermal keratinocytes. After treatment with sulindac and an oxidizing agent, cell viability, and intracellular ROS levels were measured. An open-label clinical trial was performed using sulindac and hydrogen peroxide gels daily for 3 weeks on AKs involving the upper extremities.
In SCC cells, a combination of sulindac and an oxidizing agent lead to 400 to 500% increases in intracellular ROS, which resulted in significant cell death. In sharp contrast, normal keratinocytes did not show increases in ROS levels and were not killed. A clinical trial using the combination of sulindac and hydrogen peroxide therapy in 5 patients with AKs revealed that 60% of the treated AKs responded and 50% showed no residual AK on histopathology specimens after skin biopsy.
The small number of patients and the lack of a placebo group.
Increased levels of ROS appear to be important in the selective killing of cancer cells in the presence of sulindac and oxidizing agents. Further studies are necessary to define the role of the combination of sulindac and oxidizing agent therapy in patients with AKs and skin cancer.
光化性角化病(AK)是一种皮肤癌前病变,有可能发展为鳞状细胞癌(SCC)。舒林酸是一种经美国食品药品监督管理局(FDA)批准的非甾体抗炎药(NSAID),已被证明具有临床上显著的抗癌作用。恶性细胞对氧化应激的反应可能与正常细胞不同。
确定在存在氧化剂的情况下,活性氧(ROS)增加在舒林酸抗癌机制中的作用。评估含舒林酸和过氧化氢的凝胶联合治疗AK患者的耐受性和疗效。
使用皮肤SCC细胞系和正常人表皮角质形成细胞进行细胞培养研究。在用舒林酸和氧化剂处理后,测量细胞活力和细胞内ROS水平。进行了一项开放标签的临床试验,对上肢的AK患者每天使用舒林酸和过氧化氢凝胶,持续3周。
在SCC细胞中,舒林酸和氧化剂的组合导致细胞内ROS增加400%至500%,从而导致显著的细胞死亡。形成鲜明对比的是,正常角质形成细胞未显示ROS水平升高,也未被杀死。一项对5例AK患者使用舒林酸和过氧化氢联合治疗的临床试验显示,60%的治疗后的AK有反应,50%的患者在皮肤活检后的组织病理学标本上未显示残留的AK。
患者数量少且缺乏安慰剂组。
在存在舒林酸和氧化剂的情况下,ROS水平升高似乎在选择性杀死癌细胞中起重要作用。有必要进一步研究以确定舒林酸和氧化剂联合治疗在AK和皮肤癌患者中的作用。