Li Jian, Hu Guohuang, Kong Fujiao, Wu Kemin, Song Kun, He Jianfeng, Sun Weijia
Department of PET center, Xiangya Hospital, Central South University, Changsha, China.
Pathol Oncol Res. 2015 Sep;21(4):1013-20. doi: 10.1007/s12253-015-9930-y. Epub 2015 Mar 20.
STMN1 is a cytosolic phosphoprotein that not only participates in cell division, but also plays an important role in other microtubule-dependent processes, such as cell motility. Furthermore, STMN1 acts as a "relay protein" in several intracellular signaling pathways that influence cell growth and differentiation. Thus, STMN1 is likely to support cellular processes essential for tumor progression: survival and migration. Indeed, elevated STMN1 expression has been reported in various types of human malignancies and is correlated with poor prognosis in these human malignancies. However, the clinical and prognostic significance of STMN1 in pancreatic ductal adenocarcinoma (PDAC) remains unknown. Thus, we assessed STMN1 in PDAC in this retrospective study. We first examined STMN1 expression in PDAC tissues from 27 cases and matched adjacent non-cancerous tissues by quantitative polymerase chain reaction (PCR) and western blot analyses. Next, immunohistochemistry was used to evaluate STMN1 expression in 87 archived paraffin-embedded PDAC specimens. STMN1 mRNA and protein expression levels were to a large extent up-regulated in PDAC tissue compared with their adjacent non-cancerous tissues. Moreover, STMN1 expression was closely correlated with histological differentiation, lymphatic metastasis, and TNM stage (P = 0.023, 0.047, and 0.014, respectively). In addition, PDAC patients with higher STMN1 expression died sooner than those with lower STMN1 expression (P < 0.01). Multivariate analysis demonstrated that STMN1 expression was an independent prognostic factor for PDAC patients (P < 0.01). Herein, we provide the first evidence that up-regulated STMN1 may contribute to tumor progression and poor prognosis in PDAC patients and may serve as a novel prognostic marker.
STMN1是一种胞质磷蛋白,它不仅参与细胞分裂,还在其他微管依赖过程中发挥重要作用,如细胞运动。此外,STMN1在影响细胞生长和分化的几种细胞内信号通路中充当“中继蛋白”。因此,STMN1可能支持肿瘤进展所必需的细胞过程:存活和迁移。事实上,已有报道称STMN1在各种类型的人类恶性肿瘤中表达升高,并且与这些人类恶性肿瘤的不良预后相关。然而,STMN1在胰腺导管腺癌(PDAC)中的临床和预后意义仍不清楚。因此,我们在这项回顾性研究中评估了PDAC中的STMN1。我们首先通过定量聚合酶链反应(PCR)和蛋白质印迹分析检查了27例PDAC组织及其匹配的相邻非癌组织中STMN1的表达。接下来,使用免疫组织化学评估87份存档石蜡包埋的PDAC标本中STMN1的表达。与相邻的非癌组织相比,PDAC组织中STMN1 mRNA和蛋白质表达水平在很大程度上上调。此外,STMN1表达与组织学分化、淋巴转移和TNM分期密切相关(分别为P = 0.023、0.047和0.014)。此外,STMN1表达较高的PDAC患者比STMN1表达较低的患者死亡更早(P < 0.01)。多变量分析表明,STMN1表达是PDAC患者的独立预后因素(P < 0.01)。在此,我们提供了首个证据,即STMN1上调可能导致PDAC患者的肿瘤进展和不良预后,并且可能作为一种新的预后标志物。