Sheetz Tyler, Mills Joseph, Tessari Anna, Pawlikowski Megan, Braddom Ashley E, Posid Tasha, Zynger Debra L, James Cindy, Embrione Valerio, Parbhoo Kareesma, Foray Claudia, Coppola Vincenzo, Croce Carlo M, Palmieri Dario
Department of Cancer Biology and Genetics, The Ohio State University Wexner Medical Center, Columbus, OH 43210, USA.
Comprehensive Cancer Center, The Ohio State University, Columbus, OH 43210, USA.
Cancers (Basel). 2020 Jul 10;12(7):1861. doi: 10.3390/cancers12071861.
Prostate cancer (PCa) is the most frequently diagnosed cancer in men and second most common cause of cancer-related deaths in the United States. Androgen deprivation therapy (ADT) is only temporarily effective for advanced-stage PCa, as the disease inevitably progresses to castration-resistant prostate cancer (CRPC). The protein nucleolin (NCL) is overexpressed in several types of human tumors where it is also mislocalized to the cell surface. We previously reported the identification of a single-chain fragment variable (scFv) immuno-agent that is able to bind NCL on the surface of breast cancer cells and inhibit proliferation both in vitro and in vivo. In the present study, we evaluated whether NCL could be a valid therapeutic target for PCa, utilizing DU145, PC3 (CRPC), and LNCaP (androgen-sensitive) cell lines. First, we interrogated the publicly available databases and noted that higher NCL mRNA levels are associated with higher Gleason Scores as well as with recurrent and metastatic tumors. Then, using our anti-NCL scFv, we demonstrated that NCL is expressed on the surface of all three tested cell lines and that NCL inhibition results in reduced proliferation and migration. We also measured the inhibitory effect of NCL targeting on the biogenesis of oncogenic microRNAs such as miR-21, -221 and -222, which was cell context dependent. Taken together, our data provide evidence that NCL targeting inhibits the key hallmarks of malignancy in PCa cells and may provide a novel therapeutic option for patients with advanced-stage PCa.
前列腺癌(PCa)是男性中最常被诊断出的癌症,在美国是癌症相关死亡的第二大常见原因。雄激素剥夺疗法(ADT)对晚期PCa仅具有暂时的疗效,因为该疾病不可避免地会进展为去势抵抗性前列腺癌(CRPC)。核仁素(NCL)蛋白在几种人类肿瘤中过表达,并且在这些肿瘤中它还会错误定位于细胞表面。我们之前报道了一种单链可变片段(scFv)免疫制剂的鉴定,该制剂能够结合乳腺癌细胞表面的NCL,并在体外和体内抑制其增殖。在本研究中,我们利用DU145、PC3(CRPC)和LNCaP(雄激素敏感)细胞系评估了NCL是否可能是PCa的一个有效的治疗靶点。首先,我们查询了公开可用的数据库,并注意到较高的NCL mRNA水平与较高的Gleason评分以及复发和转移性肿瘤相关。然后,使用我们的抗NCL scFv,我们证明NCL在所有三种测试的细胞系表面均有表达,并且抑制NCL会导致细胞增殖和迁移减少。我们还测量了靶向NCL对致癌性微小RNA(如miR-21、-221和-222)生物合成的抑制作用,这种作用取决于细胞环境。综上所述,我们的数据提供了证据,表明靶向NCL可抑制PCa细胞中的关键恶性特征,并可能为晚期PCa患者提供一种新的治疗选择。