Hormaechea-Agulla Daniel, Jiménez-Vacas Juan M, Gómez-Gómez Enrique, L-López Fernando, Carrasco-Valiente Julia, Valero-Rosa José, Moreno María M, Sánchez-Sánchez Rafael, Ortega-Salas Rosa, Gracia-Navarro Francisco, Culler Michael D, Ibáñez-Costa Alejandro, Gahete Manuel D, Requena María J, Castaño Justo P, Luque Raúl M
Maimonides Institute of Biomedical Research of Córdoba (IMIBIC), Cordoba, Spain.
Department of Cell Biology, Physiology, and Immunology, University of Córdoba, Cordoba, Spain.
FASEB J. 2017 Nov;31(11):4682-4696. doi: 10.1096/fj.201601264RRR. Epub 2017 Jul 13.
sst5TMD4, a splice variant of the sst5 gene, is overexpressed and associated with aggressiveness in various endocrine-related tumors, but its presence, functional role, and mechanisms of actions in prostate cancer (PCa)-the most common cancer type in males-is completely unexplored. In this study, formalin-fixed, paraffin-embedded prostate pieces from patients with localized PCa, which included tumoral and nontumoral adjacent regions ( = 45), fresh biopsies from patients with high-risk PCa ( = 52), and healthy fresh prostates from cystoprostatectomies ( = 14) were examined. In addition, PCa cell lines and xenograft models were used to determine the presence and functional role of sst5TMD4. Results demonstrated that sst5TMD4 is overexpressed (mRNA/protein) in PCa samples, and this is especially drastic in metastatic and/or high Gleason score tumor samples. Remarkably, sst5TMD4 expression was associated with an altered frequency of 2 single-nucleotide polymorphisms: rs197055 and rs12599155. In addition, PCa cell lines and xenograft models were used to demonstrate that sst5TMD4 overexpression increases cell proliferation and migration in PCa cells and induces larger tumors in nude mice, whereas its silencing decreased proliferation and migration. Remarkably, sst5TMD4 overexpression activated multiple intracellular pathways (ERK/JNK, MYC/MAX, WNT, retinoblastoma), altered oncogenes and tumor suppressor gene expression, and disrupted the normal response to somatostatin analogs in PCa cells. Altogether, we demonstrate that sst5TMD4 is overexpressed in PCa, especially in those patients with a worse prognosis, and plays an important pathophysiologic role in PCa, which suggesting its potential as a biomarker and/or therapeutic target.-Hormaechea-Agulla, D., Jiménez-Vacas, J. M., Gómez-Gómez, E., L.-López, F., Carrasco-Valiente, J., Valero-Rosa, J., Moreno, M. M., Sánchez-Sánchez, R., Ortega-Salas, R., Gracia-Navarro, F., Culler, M. D., Ibáñez-Costa, A., Gahete, M. D., Requena, M. J., Castaño, J. P., Luque, R. M. The oncogenic role of the spliced somatostatin receptor sst5TMD4 variant in prostate cancer.
sst5TMD4是sst5基因的一种剪接变体,在多种内分泌相关肿瘤中过度表达并与侵袭性相关,但它在前列腺癌(PCa)(男性最常见的癌症类型)中的存在、功能作用及作用机制完全未被探索。在本研究中,对来自局限性PCa患者的福尔马林固定、石蜡包埋前列腺组织切片(包括肿瘤及肿瘤旁非肿瘤区域,n = 45)、高危PCa患者的新鲜活检组织(n = 52)以及膀胱前列腺切除术获得的健康新鲜前列腺组织(n = 14)进行了检测。此外,还使用PCa细胞系和异种移植模型来确定sst5TMD4的存在及其功能作用。结果表明,sst5TMD4在PCa样本中过度表达(mRNA/蛋白质),在转移性和/或高Gleason评分肿瘤样本中尤为显著。值得注意的是,sst5TMD4的表达与两个单核苷酸多态性rs197055和rs12599155的频率改变相关。此外,PCa细胞系和异种移植模型被用于证明sst5TMD4的过表达会增加PCa细胞的增殖和迁移,并在裸鼠中诱导更大的肿瘤,而其沉默则会降低增殖和迁移。值得注意的是,sst5TMD4的过表达激活了多个细胞内信号通路(ERK/JNK、MYC/MAX、WNT、视网膜母细胞瘤),改变了癌基因和肿瘤抑制基因的表达,并破坏了PCa细胞对生长抑素类似物的正常反应。总之,我们证明sst5TMD4在PCa中过度表达,尤其是在预后较差的患者中,并在PCa中发挥重要的病理生理作用,这表明其作为生物标志物和/或治疗靶点的潜力。-霍马切亚 - 阿古拉,D.,希门尼斯 - 瓦卡斯,J. M.,戈麦斯 - 戈麦斯,E.,L - 洛佩斯,F.,卡拉斯科 - 瓦伦特,J.,瓦莱罗 - 罗萨,J.,莫雷诺,M. M.,桑切斯 - 桑切斯,R.,奥尔特加 - 萨拉斯,R.,格拉西亚 - 纳瓦罗,F.,卡勒,M. D.,伊瓦涅斯 - 科斯塔,A.,加埃特,M. D.,雷凯纳,M. J.,卡斯塔尼奥,J. P.,卢克,R. M. 剪接的生长抑素受体sst5TMD4变体在前列腺癌中的致癌作用