Chappell William H, Candido Saverio, Abrams Stephen L, Russo Suzanne, Ove Roger, Martelli Alberto M, Cocco Lucio, Ramazzotti Giulia, Cervello Melchiorre, Montalto Giuseppe, Steelman Linda S, Leng Xiaohong, Arlinghaus Ralph B, Libra Massimo, McCubrey James A
Department of Microbiology & Immunology, Brody School of Medicine, East Carolina University, Greenville, NC, 27834, USA; Becton, Dickinson and Company (BD), BD Diagnostics, Franklin Lakes, NJ, USA.
Department of Bio-Medical Sciences, University of Catania, Catania, Italy.
Adv Biol Regul. 2018 Aug;69:43-62. doi: 10.1016/j.jbior.2018.05.002. Epub 2018 May 18.
Neutrophil gelatinase-associated lipocalin (NGAL a.k.a lipocalin 2, lnc2) is a secreted protein which can form a complex with matrix metalloproteinase-9 (MMP9). This MMP9/NGAL complex has been associated with metastasis. MMP9 and NGAL are detected in the urine of patients afflicted with many different types of cancer, including prostate cancer. The effects of p53, NF-κB and the androgen receptor (AR) on the expression of NGAL was examined in four prostate cancer cell lines. Prostate cancer cell lines that are AR negative and expressed either mutant or no p53 (DU145 and PC3) displayed higher levels of NGAL expression compared to the prostate cancer cell lines (LNCaP and 22Rv-1) which are AR positive and express wild type (WT) p53. Introduction of WT-p53 into the PC3 prostate cancer cell line, resulted in reduction of the levels of NGAL expression. Conversely, introduction of dominant negative (DN) p53 or a retroviral construct expressing NF-κB into LNCaP cells increased NGAL expression. NGAL expression had functional effects on the ability of the cells to form colonies in soft agar. Whereas suppression of WT-53 in LNCaP cells increased NGAL expression, the introduction of WT-p53 suppressed NGAL transcription activity in PC3 prostate cells which normally express high level of NGAL. NF-κB and p53 were determined to regulate NGAL expression by positive and negative mechanisms, respectively. Our data indicate that prostate cancer growth, progression and sensitivity to chemotherapeutic drugs are regulated in part by NGAL and may involve complex interactions between NGAL, MMP9, NF-κB and p53.
中性粒细胞明胶酶相关脂质运载蛋白(NGAL,又称脂质运载蛋白2,lnc2)是一种分泌蛋白,它可以与基质金属蛋白酶-9(MMP9)形成复合物。这种MMP9/NGAL复合物与转移有关。在患有多种不同类型癌症(包括前列腺癌)的患者尿液中可检测到MMP9和NGAL。在四种前列腺癌细胞系中检测了p53、核因子κB(NF-κB)和雄激素受体(AR)对NGAL表达的影响。与AR阳性且表达野生型(WT)p53的前列腺癌细胞系(LNCaP和22Rv-1)相比,AR阴性且表达突变型p53或无p53的前列腺癌细胞系(DU145和PC3)显示出更高水平的NGAL表达。将WT-p53导入PC3前列腺癌细胞系导致NGAL表达水平降低。相反,将显性负性(DN)p53或表达NF-κB的逆转录病毒构建体导入LNCaP细胞会增加NGAL表达。NGAL表达对细胞在软琼脂中形成集落的能力具有功能影响。虽然在LNCaP细胞中抑制WT-53会增加NGAL表达,但导入WT-p53会抑制通常表达高水平NGAL的PC3前列腺细胞中的NGAL转录活性。已确定NF-κB和p53分别通过正向和负向机制调节NGAL表达。我们的数据表明,前列腺癌的生长、进展和对化疗药物的敏感性部分受NGAL调节,并且可能涉及NGAL、MMP9、NF-κB和p53之间的复杂相互作用。