Department of Urology and Pediatric Urology, Saarland University, Kirrbergerstr. 100 Gebäude 6, 66424, Homburg, Germany.
Sci Rep. 2024 Apr 17;14(1):8835. doi: 10.1038/s41598-024-59052-0.
In this study, we aimed to establish a technique for intraprostatic implantation of prostate cancer (PCa) spheroids and to identify the impact of three-dimensional organization of PCa cells on tumor progression and metastasis in a representative in vivo model. 40,000 LNCaP cells were implanted into the prostate of immunodeficient SCID mice either as single cells (n = 8) or as preformed 3D spheroids (n = 8). For a follow up of 20 weeks, tumor growth was monitored by serum PSA and high-resolution 3D ultrasonography. Eventually, animals were sacrificed and autopsied. The organ dissects were analyzed for the presence of metastases by histology (H&E) and immunohistochemistry (AMACR, AR, Ki-67, CK5, CK8, E-Cadherin, Vimentin). Solid intraprostatic tumors developed in 50% of mice after spheroid implantation and in 50% of mice after implantation of a single cells. Primary tumors of LNCaP spheroids evolved earlier, exhibiting a shorter tumor doubling time whilst developing larger tumor volumes, which was reflected by a higher immunohistochemical expression of Ki-67 and AR, too. Spheroid tumors established lung and lymph node metastases in 75% of mice, in contrast to 50% of mice after single cell implantation. Our technique enables a variety of studies regarding the influence of the tumor microenvironment on PCa progression.
在这项研究中,我们旨在建立一种前列腺癌(PCa)球体的前列腺内植入技术,并在代表性的体内模型中确定 PCa 细胞的三维组织对肿瘤进展和转移的影响。将 40000 个 LNCaP 细胞分别作为单细胞(n=8)或预形成的 3D 球体(n=8)植入免疫缺陷 SCID 小鼠的前列腺中。为了进行 20 周的随访,通过血清 PSA 和高分辨率 3D 超声监测肿瘤生长。最终,动物被处死并进行尸检。通过组织学(H&E)和免疫组织化学(AMACR、AR、Ki-67、CK5、CK8、E-钙粘蛋白、波形蛋白)分析器官解剖标本中是否存在转移。在球体植入后,50%的小鼠和单细胞植入后,50%的小鼠发展为实体性前列腺内肿瘤。LNCaP 球体的原发性肿瘤更早发展,表现出更短的肿瘤倍增时间,同时发展出更大的肿瘤体积,这反映在 Ki-67 和 AR 的免疫组织化学表达也更高。与单细胞植入后 50%的小鼠相比,球体肿瘤在 75%的小鼠中建立了肺和淋巴结转移。我们的技术使各种研究能够研究肿瘤微环境对 PCa 进展的影响。