The effects of meloxicam, lornoxicam, ketoprofen, and dexketoprofen on human cervical, colorectal, and mammary carcinoma cell lines

Lyubomir Marinov, A. Georgieva, R. Toshkova, Ivanka Kostadinova, I. Mangarov, Tanya Toshkova-Yotova, Irina Nikolova
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Abstract

Targeting the inflammation-related molecules with nonsteroidal anti-inflammatory drugs (NSAIDs) represents a promising approach for cancer prevention/therapy. We evaluated the in vitro anticancer effects of meloxicam, lornoxicam, ketoprofen, and dexketoprofen on the proliferation, migration, and apoptosis of human cervical, colorectal, and mammary carcinoma cells. The antiproliferative activity and cytotoxicity of tested NSAIDs on HeLa, HT-29, and MCF-7 cell lines were assessed by the MTT test. The apoptosis-inducing potential was analyzed by fluorescent staining with acridine orange/ethidium bromide and DAPI. Migration activity was assessed by a wound-healing scratch assay. The tested NSAIDs reduced the viability of the used tumor cell lines. The cytomorphological analysis revealed reduced cell density and mitotic activity and the presence of cells with morphological features of early and late apoptosis. Significant inhibition of the migration capacity was established as well. In conclusion, NSAIDs could be candidates for the development of new pharmacological strategies for the treatment and prevention of cancer.
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美洛昔康、洛诺昔康、酮洛芬和右酮洛芬对人类宫颈癌、结直肠癌和乳腺癌细胞系的影响
用非甾体抗炎药(NSAIDs)靶向炎症相关分子是一种很有前景的癌症预防/治疗方法。我们评估了美洛昔康、洛诺昔康、酮洛芬和右酮洛芬对人宫颈癌、结直肠癌和乳腺癌细胞的增殖、迁移和凋亡的体外抗癌作用。通过 MTT 试验评估了受试非甾体抗炎药对 HeLa、HT-29 和 MCF-7 细胞系的抗增殖活性和细胞毒性。用吖啶橙/溴化乙锭和 DAPI 进行荧光染色,分析诱导细胞凋亡的潜力。迁移活性通过伤口愈合划痕试验进行评估。测试的非甾体抗炎药降低了所用肿瘤细胞系的活力。细胞形态学分析表明,细胞密度和有丝分裂活性降低,出现了具有早期和晚期凋亡形态特征的细胞。迁移能力也受到明显抑制。总之,非甾体抗炎药可作为开发治疗和预防癌症新药理策略的候选药物。
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