Instituto de Pesquisa e Desenvolvimento, Laboratório de Dinâmica de Compartimentos Celulares, Universidade do Vale do Paraíba, São José dos Campos, SP, Brasil.
Instituto de Pesquisa e Desenvolvimento, Laboratório de Fotobiologia Aplicada è Saúde, Universidade do Vale do Paraíba, São José dos Campos, SP, Brasil.
Braz J Med Biol Res. 2024 Nov 4;57:e14129. doi: 10.1590/1414-431X2024e14129. eCollection 2024.
Epithelial cancers, such as epidermoid cancer and some adenocarcinomas, affect surface areas that are generally more accessible to various treatments. However, this group of tumor cells has an aggressive behavior, leading to a high annual mortality rate. The development of a biomaterial that is non-invasive, can kill tumor cells, and prevent opportunistic infections is the basis for the treatment for this type of cancer. Therefore, the objective of this study was to develop a biomaterial from chitosan and A. oleracea extracts that exhibits cytotoxic action against the HEp-2 tumor cell line. Dried crude 90% ethanol extracts were obtained through ultrasound-assisted maceration, followed by liquid-liquid extraction to yield the butanol fraction. From these extracts, chitosan membranes were developed and evaluated for their antitumor activity against HEp-2 using viability tests with crystal violet and MTT (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide) assay, in addition to a wound healing test. The cytotoxic assays indicated a significant reduction in cell density and mitochondrial activity, especially at the concentration of 1000 µg/mL of crude extract. The butanol fraction had minimal effects on mitochondrial activity. The wound healing test demonstrated that the biomaterial and extract prevented closure of the wound created in the cell monolayer within 48 h of incubation and caused changes in cell morphology. In view of this, we concluded that a chitosan membrane associated with a 90% ethanol extract of Acmella oleracea exhibited cytotoxic activity is a potential alternative treatment for superficial cancers.
上皮癌,如表皮样癌和某些腺癌,影响到通常更容易接受各种治疗的表面区域。然而,这组肿瘤细胞具有侵袭性的行为,导致每年的高死亡率。开发一种非侵入性的生物材料,能够杀死肿瘤细胞并预防机会性感染,是治疗这种类型癌症的基础。因此,本研究的目的是开发一种由壳聚糖和 A.oleracea 提取物制成的生物材料,该材料对 HEp-2 肿瘤细胞系具有细胞毒性作用。通过超声辅助浸渍法获得干燥的粗 90%乙醇提取物,然后进行液-液萃取以得到丁醇级分。从这些提取物中开发出壳聚糖膜,并通过结晶紫和 MTT(3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四氮唑溴盐)测定法对其针对 HEp-2 的抗肿瘤活性进行评估,此外还进行了伤口愈合试验。细胞毒性试验表明,细胞密度和线粒体活性显著降低,特别是在粗提取物浓度为 1000 µg/mL 时。丁醇级分对线粒体活性的影响最小。伤口愈合试验表明,生物材料和提取物在孵育 48 小时内阻止了细胞单层中形成的伤口闭合,并导致细胞形态发生变化。鉴于此,我们得出结论,与 Acmella oleracea 的 90%乙醇提取物相关的壳聚糖膜具有细胞毒性活性,是治疗浅表癌症的潜在替代方法。