Che Jian-Ping, Li Wei, Yan Yang, Liu Min, Wang Guang-Chun, Li Qian-Yu, Yang Bin, Yao Xu-Dong, Zheng Jun-Hua
Department of Urology, Shanghai Tenth People's Hospital, Tongji University Shanghai, 200072, China.
Int J Clin Exp Pathol. 2013 Oct 15;6(11):2300-11. eCollection 2013.
Prostate carcinoma is a major cause of morbidity and mortality. The MAPK Signaling Pathway plays an important role in multiple tumors, including prostate carcinoma. MAPK signaling is mediated by ERK1/2, JNK and p38 MAPK, which are important in the control of cell proliferation, differentiation and apoptosis. However, relatively little is known about the regulatory mechanism of p38 MAPK in prostate cancers. NOB1 is among the most novel topic in MAPK studies currently. Recent studies found its vital role in tumor metastasis in glioblastoma proliferation, however, its expression profile and its prognostic value in prostate carcinoma have not been investigated.
To determine the relationship between NOB1 and p38 MAPK expressions, a population-based study was conducted for immunohistochemical staining analysis of tumor tissues, in matched malignant and nonmalignant prostatectomy samples from 132 PCa patients. Moreover, Western blot analysis and NOB1 interference studies of prostate cancer cell lines. To evaluate the diagnostic and prognostic between NOB1 and p38 MAPK in prostate cancer (PCa) tissue after radical prostatectomy, the hypothesis that prostate cancers with NOB1 expression have distinct clinical, prognostic and molecular attributes was tested.
Among 132 prostate cancers, NOB1 expression was detected in 117 (88.7%) tumors by immunohistochemistry. NOB1 and p38 MAPK expression had significant positive correlation with carcinogenesis, tumor progression and patient survival. Immunohistochemically, NOB1 expression in prostate cancer was independently associated with p38 MAPK activation (P=0.0002). Furthermore, p38 MAPK expression was completely suppressed by NOB1 interference in the prostate cancer cell lines DU-145 and PC-3.
NOB1 expression status was closely correlated with important histopathologic characteristics and the recurrence and metastasis of prostate carcinomas. These data support a potential link between NOB1 and p38 MAPK, and suggest that NOB1 may identify a subset of prostate cancer patients with a poor prognosis. This study proved that NOB1 in PCa tissue can be used, in combination with traditional clinicopathological factors, as promising diagnostic and prognostic tools.
前列腺癌是发病和死亡的主要原因。丝裂原活化蛋白激酶(MAPK)信号通路在包括前列腺癌在内的多种肿瘤中发挥重要作用。MAPK信号由细胞外信号调节激酶1/2(ERK1/2)、应激活化蛋白激酶(JNK)和p38 MAPK介导,它们在细胞增殖、分化和凋亡的控制中起重要作用。然而,关于p38 MAPK在前列腺癌中的调控机制相对知之甚少。NOB1是目前MAPK研究中最新的课题之一。最近的研究发现其在胶质母细胞瘤增殖的肿瘤转移中起重要作用,然而,其在前列腺癌中的表达谱及其预后价值尚未得到研究。
为了确定NOB1与p38 MAPK表达之间的关系,对132例前列腺癌患者配对的恶性和非恶性前列腺切除样本的肿瘤组织进行了基于人群的免疫组织化学染色分析。此外,对前列腺癌细胞系进行了蛋白质印迹分析和NOB1干扰研究。为了评估根治性前列腺切除术后前列腺癌(PCa)组织中NOB1和p38 MAPK的诊断和预后价值,检验了NOB1表达的前列腺癌具有独特的临床、预后和分子特征这一假设。
在132例前列腺癌中,通过免疫组织化学在117例(88.7%)肿瘤中检测到NOB1表达。NOB1和p38 MAPK表达与致癌作用、肿瘤进展和患者生存呈显著正相关。免疫组织化学显示,前列腺癌中NOB1表达与p38 MAPK激活独立相关(P=0.0002)。此外,在前列腺癌细胞系DU-145和PC-3中,NOB1干扰完全抑制了p38 MAPK表达。
NOB1表达状态与前列腺癌的重要组织病理学特征以及复发和转移密切相关。这些数据支持了NOB1与p38 MAPK之间的潜在联系,并表明NOB1可能识别出预后不良的前列腺癌患者亚组。本研究证明,PCa组织中的NOB1可与传统临床病理因素联合使用,作为有前景的诊断和预后工具。