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A 3D biofabricated cutaneous squamous cell carcinoma tissue model with multi-channel confocal microscopy imaging biomarkers to quantify antitumor effects of chemotherapeutics in tissue

机译:具有多通道共聚焦显微镜成像生物标记物的3D生物制造的皮肤鳞状细胞癌组织模型以量化组织中化学疗法的抗肿瘤作用

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摘要

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.
机译:在美国,皮肤鳞状细胞癌(cSCC)每年导致约10,000人死亡。当前的疗法对转移性和局部晚期cSCC无效。需要鉴定新颖,有效且毒性较小的小分子cSCC治疗剂。我们开发了cSCC肿瘤的3维生物打印皮肤(3DBPS)模型以及显微镜检测法,以测试组织中的化学治疗作用。使用苏木精和曙红(H&E)以及免疫组织化学组织学染色,共聚焦显微镜和cDNA微阵列分析验证了完整厚度的SCC组织模型。开发了一种使用tdTomato标记的A431 SCC和ZsGreen标记的角质形成细胞的非破坏性3D荧光共聚焦成像试验,以测试化学疗法的功效和一般毒性。荧光衍生的成像生物标记物表明,在1μM5-氟尿嘧啶48小时治疗后,组织中有50%的癌细胞被杀死,而未治疗的对照组的基线为12%。成像生物标记物还显示,正常角质形成细胞受治疗的影响(杀死的11%)比未治疗的组织少,后者没有明显的杀伤作用。数据显示5-氟尿嘧啶比角质形成细胞更有选择性地杀死cSCC细胞。我们的3DBPS分析平台可对细胞活力进行细胞水平的测量,并可用于在生物制品组织中实现无损高通量筛选(HTS)。

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