Browning James R, Derr Paige, Derr Kristy, Doudican Nicole, Michael Sam, Lish Samantha R, Taylor Nicholas A, Krueger James G, Ferrer Marc, Carucci John A, Gareau Daniel S
Laboratory for Investigative Dermatology, The Rockefeller University, New York, New York, USA.
National Center for Advancing Translational Sciences, National Institutes of Health, Rockville, Maryland, USA.
Oncotarget. 2020 Jul 7;11(27):2587-2596. doi: 10.18632/oncotarget.27570.
Cutaneous squamous cell carcinoma (cSCC) causes approximately 10,000 deaths annually in the U. S. Current therapies are largely ineffective against metastatic and locally advanced cSCC. There is a need to identify novel, effective, and less toxic small molecule cSCC therapeutics. We developed a 3-dimensional bioprinted skin (3DBPS) model of cSCC tumors together with a microscopy assay to test chemotherapeutic effects in tissue. The full thickness SCC tissue model was validated using hematoxylin and eosin (H&E) and immunohistochemical histological staining, confocal microscopy, and cDNA microarray analysis. A nondestructive, 3D fluorescence confocal imaging assay with tdTomato-labeled A431 SCC and ZsGreen-labeled keratinocytes was developed to test efficacy and general toxicity of chemotherapeutics. Fluorescence-derived imaging biomarkers indicated that 50% of cancer cells were killed in the tissue after 1μM 5-Fluorouracil 48-hour treatment, compared to a baseline of 12% for untreated controls. The imaging biomarkers also showed that normal keratinocytes were less affected by treatment (11% killed) than the untreated tissue, which had no significant killing effect. Data showed that 5-Fluorouracil selectively killed cSCC cells more than keratinocytes. Our 3DBPS assay platform provides cellular-level measurement of cell viability and can be adapted to achieve nondestructive high-throughput screening (HTS) in bio-fabricated tissues.
皮肤鳞状细胞癌(cSCC)在美国每年导致约10000人死亡。目前的治疗方法对转移性和局部晚期cSCC大多无效。需要鉴定新型、有效且毒性较小的小分子cSCC治疗药物。我们开发了一种cSCC肿瘤的三维生物打印皮肤(3DBPS)模型以及一种显微镜检测方法,以测试组织中的化疗效果。使用苏木精和伊红(H&E)以及免疫组织化学组织学染色、共聚焦显微镜和cDNA微阵列分析对全层SCC组织模型进行了验证。开发了一种用tdTomato标记的A431 SCC和ZsGreen标记的角质形成细胞的非破坏性三维荧光共聚焦成像检测方法,以测试化疗药物的疗效和一般毒性。荧光衍生的成像生物标志物表明,在1μM 5-氟尿嘧啶48小时治疗后,组织中50%的癌细胞被杀死,而未治疗对照组的基线为12%。成像生物标志物还表明,正常角质形成细胞受治疗的影响较小(11%被杀死),而未治疗的组织则没有明显的杀伤作用。数据表明,5-氟尿嘧啶对cSCC细胞的选择性杀伤作用大于角质形成细胞。我们的3DBPS检测平台提供了细胞活力的细胞水平测量,并且可以进行调整以在生物制造的组织中实现非破坏性高通量筛选(HTS)。