Department of Structural and Functional Biology, Institute of Biology, University of Campinas (UNICAMP), Campinas, SP, Brazil.
Microsc Res Tech. 2013 Mar;76(3):321-30. doi: 10.1002/jemt.22170. Epub 2013 Jan 30.
The objective was to characterize and associate the receptor reactivities of fibroblastic growth factor (FGF)-2, FGF-7, FGF-8, epidermal growth factor (EGF), α-actin and vimentin in relation to the androgen receptor (AR), α and β estrogen receptors (ERα and ERβ), and prolactin receptor in the prostate of elderly men showing low- and high-grade adenocarcinoma. Thirty prostatic samples were taken from 60- to 90-year-old patients without prostatic lesions and with low-grade cancer and high-grade cancer, from the University Hospital, School of Medicine, the State University of Campinas. The results showed that increased FGF-2, FGF-7, and FGF-8 receptor reactivities and decreased AR reactivity were verified in both high- and low-grade cancer. However, the FGF-8 receptor showed greater involvement at the beginning of the malignancy alterations. Increased EGF receptor (EGFR) reactivity and diminished α-actin immunohistochemistry were identified in both cancer groups. Also, increased ERα, PR, and vimentin receptors were verified in both cancer groups. To conclude, the ERα involvement in the reactive stroma activation led to a microenvironment, which was favorable to cancer progression, due to maximizing stromal imbalance. The prolactin could be related to cancer progression due to its interaction with ERα action, indicating that this hormone could be a relevant target to prevent the estrogenic effects in the prostatic lesions. Both FGF receptor (FGFR)-2 and FGFR-8 play a fundamental role in the early stages of prostate cancer, suggesting that these molecules could be a promising therapeutic target. The differential localization of the fibroblastic factors between the prostatic epithelium and stroma of elderly men, who presented prostate cancer, could indicate a favorable distinction for tumoral progression.
目的是描述和关联成纤维细胞生长因子 (FGF)-2、FGF-7、FGF-8、表皮生长因子 (EGF)、α-肌动蛋白和波形蛋白与雄激素受体 (AR)、α 和β雌激素受体 (ERα 和 ERβ) 以及催乳素受体在老年男性前列腺中的反应性,这些男性表现出低级别和高级别腺癌。从坎皮纳斯州立大学医学院大学医院获取了 30 个前列腺样本,这些样本来自 60 至 90 岁的无前列腺病变且患有低级别和高级别癌症的患者。结果表明,在高级别和低级别癌症中均证实 FGF-2、FGF-7 和 FGF-8 受体反应性增加和 AR 反应性降低。然而,FGF-8 受体在恶性肿瘤改变的早期阶段显示出更大的相关性。在两个癌症组中均发现 EGF 受体 (EGFR) 反应性增加和α-肌动蛋白免疫组织化学减少。此外,在两个癌症组中均证实 ERα、PR 和波形蛋白受体增加。总之,由于最大限度地增加了基质失衡,ERα 参与反应性基质激活导致了有利于癌症进展的微环境。催乳素可能与癌症进展有关,因为它与 ERα 作用相互作用,表明这种激素可能是预防前列腺病变中雌激素作用的一个相关靶点。FGF 受体 (FGFR)-2 和 FGFR-8 在前列腺癌的早期阶段发挥着重要作用,表明这些分子可能是一个有前途的治疗靶点。在患有前列腺癌的老年男性的前列腺上皮和基质之间,纤维母细胞因子的差异定位可能表明肿瘤进展有良好的区别。