Montico Fabio, Kido Larissa Akemi, Hetzl Amanda Cia, Lorencini Raísa Mistieri, Cândido Eduardo Marcelo, Cagnon Valéria Helena Alves
Department of Structural and Functional Biology, Institute of Biology, University of Campinas (UNICAMP), P.O. Box 6109, Campinas, São Paulo, 13083-865, Brazil.
Histochem Cell Biol. 2014 Sep;142(3):269-84. doi: 10.1007/s00418-014-1193-2. Epub 2014 Feb 22.
Senescence is associated with hormonal imbalance and prostatic disorders. Angiogenesis is fundamental for the progression of malignant lesions and is a promising target for prostate cancer treatment. The aim was to characterize matrix metalloproteinase-9 (MMP-9) and insulin-like growth factor receptor-1 (IGFR-1) responses in the prostate during senescence and following antiangiogenic and/or androgen ablation therapies, comparing them to cancer progression features in TRAMP mice. Aged male mice (52-week-old FVB) were submitted to antiangiogenic treatments with SU5416 (6 mg/kg; i.p.) and/or TNP-470 (15 mg/kg; s.c). Finasteride (20 mg/kg; s.c.) was administered alone or associated to both inhibitors. Dorsolateral prostate was collected for light microscopy, and immunohistochemistry and Western blotting collected for MMP-9 and IGFR-1. Senescence led to inflammation and different proliferative lesions in the prostate, as well as to increased MMP-9 and IGFR-1, resembling TRAMP mice prostatic microenvironment. Antiangiogenic therapies promoted recovery and/or interruption of age-associated alterations, presenting differential effects on the molecules studied. SU5416 acted mainly on MMP-9, whereas TNP-470 showed its best influence on IGFR-1 levels. Finasteride administration, alone or in combination with antiangiogenic agents, also resulted in regression of inflammation and neoplastic lesions, besides having a negative modulatory effect on both MMP-9 and IGFR-1. We concluded that stimulated tissue remodeling and proliferative processes during senescence predisposed the prostate to malignant disorders. The combination of different agents was more effective to minimize prostatic imbalance during this period, probably due to the differential action of each drug on factors involved in cell proliferation and extracellular matrix remodeling, resulting in a broader spectrum of effects following the combined treatment.
衰老与激素失衡及前列腺疾病相关。血管生成是恶性病变进展的基础,也是前列腺癌治疗的一个有前景的靶点。本研究旨在表征衰老过程中以及抗血管生成和/或雄激素剥夺治疗后前列腺中基质金属蛋白酶-9(MMP-9)和胰岛素样生长因子受体-1(IGFR-1)的反应,并将其与TRAMP小鼠的癌症进展特征进行比较。将老年雄性小鼠(52周龄FVB)用SU5416(6mg/kg;腹腔注射)和/或TNP-470(15mg/kg;皮下注射)进行抗血管生成治疗。非那雄胺(20mg/kg;皮下注射)单独给药或与两种抑制剂联合使用。收集背外侧前列腺进行光学显微镜检查,并收集免疫组织化学和蛋白质印迹用于检测MMP-9和IGFR-1。衰老导致前列腺炎症和不同的增殖性病变,以及MMP-9和IGFR-1增加,类似于TRAMP小鼠的前列腺微环境。抗血管生成疗法促进与年龄相关改变的恢复和/或中断,对所研究分子呈现不同影响。SU5416主要作用于MMP-9,而TNP-470对IGFR-1水平影响最佳。非那雄胺单独给药或与抗血管生成药物联合使用,除了对MMP-9和IGFR-1具有负调节作用外,还导致炎症和肿瘤性病变消退。我们得出结论,衰老过程中受刺激的组织重塑和增殖过程使前列腺易患恶性疾病。不同药物联合使用在此期间更有效地减少前列腺失衡,可能是由于每种药物对参与细胞增殖和细胞外基质重塑的因子具有不同作用,联合治疗后产生更广泛的效应谱。