Department of Orthopaedic Surgery, North Shore-Long Island Jewish Hospital, Northwell Health System, 270-05 76th Avenue, New Hyde Park, NY, 11040, USA.
Orthopaedic Research Laboratory, The Feinstein Institute for Medical Research, 350 Community Drive, Manhasset, NY, 11030, USA.
J Orthop Surg Res. 2020 Mar 5;15(1):94. doi: 10.1186/s13018-020-01606-9.
5-Aminolevulinic acid (5-ALA), a fluorescent contrast agent, has been used for tumor paint and photodynamic therapy (PDT) for various tumors, but its use with soft tissue sarcomas is not well documented. Myxofibrosarcoma, a subtype of soft tissue sarcoma with a high local recurrence rate, may benefit from similar types of treatment. The purpose of this study was to analyze the effects of 5-ALA tumor paint and PDT on a myxofibrosarcoma cell line.
Tumor paint was assessed by exposing micromass pellets of human adipose-derived stromal (ADS) cells or myxofibrosarcoma (MUG-Myx1) cells to 5-ALA. Cell pellets were then visualized using a microscope at established excitation and emission wavelengths. Corrected total cell fluorescence was calculated per accepted protocols. Photodynamic therapy was similarly assessed by exposing ADS and MUG-Myx1 cells to 5-ALA, with subsequent analysis via flow cytometry and real-time confocal microscopy.
The use of 5-ALA tumor paint led to a selective fluorescence in MUG-Myx1 cells. Findings were confirmed by flow cytometry. Interestingly, flow cytometry results showed progressive selective cell death with increasing 5-ALA exposure as a result of the PDT effect. PDT was further confirmed using confocal microscopy, which revealed progressive cellular bubble formation consistent with advancing stages of cell death-a finding that was not seen in control ADS cells.
5-ALA tumor paint and PDT were successfully used on a human myxofibrosarcoma cell line (MUG-Myx1). Results from this study showed both selective fluorescent tagging and selective cytotoxicity of 5-ALA toward malignant myxofibrosarcoma cells, while sparing benign adipose control cells. This finding was further confirmed in a dramatic time-lapse video, visually confirming active, targeted cell death. 5-ALA's two-pronged application of selective tumor identification and cytotoxicity may transform surgical and medical approaches for treating soft tissue sarcomas.
5-氨基酮戊酸(5-ALA)是一种荧光对比剂,已被用于各种肿瘤的肿瘤染色和光动力疗法(PDT),但在软组织肉瘤中的应用尚未得到充分记录。黏液纤维肉瘤是一种软组织肉瘤亚型,具有较高的局部复发率,可能受益于类似的治疗方法。本研究旨在分析 5-ALA 肿瘤染色和 PDT 对黏液纤维肉瘤细胞系的影响。
通过将人脂肪来源基质(ADS)细胞或黏液纤维肉瘤(MUG-Myx1)细胞的微团暴露于 5-ALA 来评估肿瘤染色。然后使用显微镜在既定的激发和发射波长下观察细胞团。根据公认的方案计算校正的总细胞荧光。类似地,通过将 ADS 和 MUG-Myx1 细胞暴露于 5-ALA 来评估光动力疗法,随后通过流式细胞术和实时共聚焦显微镜进行分析。
使用 5-ALA 肿瘤染色导致 MUG-Myx1 细胞出现选择性荧光。通过流式细胞术证实了这一发现。有趣的是,随着 PDT 效应的增加,随着 5-ALA 暴露的增加,流式细胞术结果显示出进行性的选择性细胞死亡。通过共聚焦显微镜进一步证实了 PDT,该显微镜显示出与细胞死亡进展阶段一致的渐进性细胞气泡形成——这在对照 ADS 细胞中没有发现。
成功地在人黏液纤维肉瘤细胞系(MUG-Myx1)上使用了 5-ALA 肿瘤染色和 PDT。本研究结果表明,5-ALA 对恶性黏液纤维肉瘤细胞具有选择性荧光标记和细胞毒性,同时对良性脂肪对照细胞无害。这一发现在一段生动的延时视频中得到了进一步证实,该视频直观地证实了活跃的、靶向性的细胞死亡。5-ALA 的双重应用,即选择性肿瘤识别和细胞毒性,可能会改变治疗软组织肉瘤的手术和医疗方法。