卡波扎尼布
医学
无容量
肾细胞癌
肾透明细胞癌
肿瘤微环境
癌症研究
间质细胞
免疫系统
癌症
肾癌
免疫检查点
免疫疗法
靶向治疗
癌细胞
肿瘤科
内科学
免疫学
作者
Laura Esser,Vittorio Branchi,Sonia Leonardelli,Natalie Pelusi,Adrian Georg Simon,Niklas Klümper,Jörg Ellinger,Stefan Hauser,Maria A. Gonzalez‐Carmona,Manuel Ritter,Glen Kristiansen,Hubert Schorle,Michael Hölzel,Marieta Toma
标识
DOI:10.3389/fonc.2020.01775
摘要
Clear cell renal cell carcinoma (ccRCC) is the most common renal cancer accounting for 80% of all renal cancers as well as the majority of renal cancer-associated deaths. During the last decade, the treatment paradigm for ccRCC has radically changed. In particular, the recent development of immune checkpoint inhibitors has led to an increased overall survival in the metastatic setting. Moreover, novel immune therapies targeting the tumor microenvironment have been developed. In this rapidly evolving treatment landscape, precise tools for personalized cancer therapy are needed. Here, we collected fresh tissue from 42 patients who underwent surgical resection for renal cell carcinoma. Part of the tissue was used to obtain formalin-fixed, paraffin-embedded samples or RNA. The remaining tissue was minced and cultured in a collagen-based three-dimensional, air-liquid interface (ALI) culture system. The generated patient-derived tumor organoids (ALI PDOs) were characterized by immunohistochemistry staining and RNA sequencing to validate their close similarity to the matched tumor. Immune cells and stromal cells within the microenvironment could be identified. Finally, we treated 10 ALI PDOs with the commonly used targeted cancer drug cabozantinib or the immune checkpoint inhibitor nivolumab. Interestingly, we observed varying responses of ALI PDOs to these treatments and future studies are needed to investigate whether the ALI PDO approach could inform about treatment responses in patients. In conclusion, this three-dimensional ccRCC culture model represents a promising, facile tool for monitoring tumor responses to different types of therapies in a controlled manner, yet, still preserves the key features of the tumor of origin.
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