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一种具有多通道共聚焦显微镜成像生物标志物的3D生物制造皮肤鳞状细胞癌组织模型,用于量化化疗药物在组织中的抗肿瘤作用。

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

作者信息

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

机构信息

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.

出版信息

Oncotarget. 2020 Jul 7;11(27):2587-2596. doi: 10.18632/oncotarget.27570.

Abstract

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.

摘要

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)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/080f/7343636/f3d09d679461/oncotarget-11-2587-g001.jpg

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