Department of Tumour Biology, University Medical Centre Hamburg-Eppendorf, Hamburg, Germany; FIRC (Italian Foundation for Cancer Research) Institute of Molecular Oncology (IFOM), Milan, Italy.
Laboratory of Cell Biology, Department of Medical Biotechnology, Intercollegiate Faculty of Biotechnology, University of Gdańsk and Medical University of Gdańsk, Gdańsk, Poland.
Transl Res. 2019 Jan;203:49-56. doi: 10.1016/j.trsl.2018.08.007. Epub 2018 Sep 12.
Aldehyde dehydrogenase 1 (ALDH1) characterizes tumor-initiating cells in solid tumors; however, little is known about its expression in intratumoral stromal cells. Herein, we aimed to dissect its potential dual relevance in prostate cancer (PCa). ALDH1 expression was evaluated immunohistochemically in tumor and stromal cells in primary PCa and metastases. It was correlated to clinico-pathologic parameters, patients' outcome, and selected proteins (CK5/6, CK14, CK8/18, CK19, EpCAM, Ki-67, E-cadherin, N-cadherin, and vimentin). ALDH1 protein was detected in tumor and stromal cells in 16% and 67% of 348 primary PCa, respectively. Tumor cell ALDH1 expression was associated with advanced T stage (P = 0.009), higher Gleason score (P = 0.016), shorter time to biochemical recurrence (TBR P = 0.010) and CK14 expression (P = 0.023). Stromal cell ALDH1 expression correlated to lower T stage (P = 0.008) and Gleason score (P = 0.016), N0 stage (P = 0.017), and longer TBR (P = 0.017). It occurred to be an independent predictor of good prognosis in the subgroup of d'Amico high-risk patients (multivariate analysis, P = 0.050). ALDH1-positive stromal cells were found in tumors characterized frequently by CK8/18 (P = 0.033) or EpCAM expression (P < 0.001) and rarely by epithelial-mesenchymal transition defined as CK8/18(-)vimentin(+) phenotype (P = 0.003). ALDH1-positive tumor and stromal cells were detected in 33% and 41% of hormone naive lymph node metastases (n = 63), 52% and 24% of castration resistant bone metastases, as well as 89% and 28% of castration resistant visceral metastases (n = 21), respectively. We have determined that contrary to tumor cell ALDH1, the presence of stromal ALDH1 is associated with epithelial phenotype of primary PCa, improved clinical outcome, and is less frequent in PCa metastases.
醛脱氢酶 1(ALDH1)在实体瘤中特征性地表达于肿瘤起始细胞;然而,其在肿瘤间质细胞中的表达情况知之甚少。在此,我们旨在探讨其在前列腺癌(PCa)中的潜在双重相关性。我们通过免疫组化方法检测了原发性 PCa 和转移灶中肿瘤细胞和间质细胞中的 ALDH1 表达情况。并将其与临床病理参数、患者预后和一些特定蛋白(CK5/6、CK14、CK8/18、CK19、EpCAM、Ki-67、E-钙黏蛋白、N-钙黏蛋白和波形蛋白)进行了相关性分析。在 348 例原发性 PCa 中,肿瘤细胞和间质细胞中分别有 16%和 67%检测到 ALDH1 蛋白。肿瘤细胞 ALDH1 表达与较高的 T 分期(P = 0.009)、较高的 Gleason 评分(P = 0.016)、较短的生化复发时间(TBR,P = 0.010)和 CK14 表达(P = 0.023)相关。间质细胞 ALDH1 表达与较低的 T 分期(P = 0.008)和 Gleason 评分(P = 0.016)、N0 分期(P = 0.017)和较长的 TBR(P = 0.017)相关。在 d'Amico 高危患者亚组中,ALDH1 阳性的间质细胞是独立的预后良好的预测因子(多变量分析,P = 0.050)。ALDH1 阳性的间质细胞常伴有 CK8/18(P = 0.033)或 EpCAM 表达(P < 0.001),而少见上皮-间充质转化(定义为 CK8/18(-)vimentin(+) 表型,P = 0.003)。在激素敏感的淋巴结转移灶(n = 63)中,ALDH1 阳性的肿瘤细胞和间质细胞分别占 33%和 41%,在去势抵抗的骨转移灶中分别占 52%和 24%,在去势抵抗的内脏转移灶中分别占 89%和 28%(n = 21)。我们发现,与肿瘤细胞 ALDH1 相反,间质 ALDH1 的存在与原发性 PCa 的上皮表型、改善的临床结局相关,并且在 PCa 转移灶中较少见。