Robertson C A, Abrahamse H, Evans Denise
Laser Research Centre, Faculty of Health Sciences, University of Johannesburg, P.O. Box 17011, Doornfontein 2028, Johannesburg, South Africa.
Lasers Surg Med. 2010 Dec;42(10):766-76. doi: 10.1002/lsm.20980.
Numerous worldwide clinical trials have shown that photodynamic therapy (PDT) represents an effective and safe modality for various skin disorders, but little research has been done in terms of its effect on malignant melanomas (MM). Thus, the aim of this study was to compare the effect of both established porphyrin photosensitizer 5-aminolevulinic acid (5-ALA) and novel metallophthalocyanine (MPc) photosensitizer on human metastatic skin cells which produce a MM.
The cellular responses following PDT were assessed using changes in cell morphology, cell viability, cytotoxicity, apoptosis, and proliferation.
Findings reported that in vitro human MM cell line A375 (EACC no: 88113005) are highly sensitive to growth inhibition and apoptosis induction by the cytotoxic side-effects induced by MPc and 5-ALA photosensitizing treatments post-laser irradiation at 680 and 636 nm, respectively. The decrease of cell viability accompanied by an increased cytotoxicity and apoptotic and necrotic levels, with a time-dependant decrease in cellular proliferation was found to be far more significant for MPc-treated cells than 5-ALA-treated cells, since MPc was applied in far lower concentrations and exhibited far less photoxicity to control cells.
Hence, novel MPc proved to be the better photosensitizing dye for metastatic melanoma tumor destruction in combination with laser irradiation and is a particularly attractive photosensitizer since it exhibits so many ideal properties of a photosensitizing agent, thus further research of this possible anticancer agent could contribute to its potential application in PDT cancer treatment of MMs.
全球众多临床试验表明,光动力疗法(PDT)是治疗多种皮肤疾病的一种有效且安全的方法,但关于其对恶性黑色素瘤(MM)的影响,相关研究较少。因此,本研究旨在比较已确立的卟啉光敏剂5-氨基酮戊酸(5-ALA)和新型金属酞菁(MPc)光敏剂对产生MM的人转移性皮肤细胞的影响。
通过细胞形态、细胞活力、细胞毒性、凋亡和增殖的变化来评估PDT后的细胞反应。
研究结果表明,体外人MM细胞系A375(EACC编号:88113005)对分别在680和636nm激光照射后MPc和5-ALA光敏处理诱导的细胞毒性副作用所导致的生长抑制和凋亡诱导高度敏感。发现细胞活力下降伴随着细胞毒性、凋亡和坏死水平的增加,且细胞增殖随时间下降,MPc处理的细胞比5-ALA处理的细胞更为显著,因为MPc的应用浓度低得多,且对对照细胞的光毒性小得多。
因此,新型MPc与激光照射联合使用时,被证明是用于转移性黑色素瘤肿瘤破坏的更好的光敏染料,并且是一种特别有吸引力的光敏剂,因为它具有光敏剂的许多理想特性,因此对这种可能的抗癌剂的进一步研究可能有助于其在MM的PDT癌症治疗中的潜在应用。