The clinicopathological significance of forkhead box P1 and forkhead box O3a in pancreatic ductal adenocarcinomas

被引:11
作者
Luo, Xin [1 ]
Yang, Zhulin [2 ]
Liu, Xiao [2 ]
Liu, Ziru [2 ]
Miao, Xiongying [2 ]
Li, Daiqiang [1 ]
Zou, Qiong [3 ]
Yuan, Yuan [3 ]
机构
[1] Cent South Univ, Xiangya Hosp 2, Dept Pathol, Changsha, Hunan, Peoples R China
[2] Cent South Univ, Xiangya Hosp 2, Res Lab Hepatobiliary Dis, 139 Renmin Rd, Changsha 410011, Hunan, Peoples R China
[3] Cent South Univ, Xiangya Hosp 3, Dept Pathol, Changsha, Hunan, Peoples R China
关键词
Pancreatic ductal adenocarcinoma; dysplasia; pancreatic intraepithelial neoplasia; forkhead box P1; forkhead box O3a; immunohistochemistry; FOXO TRANSCRIPTION FACTORS; TUMOR-SUPPRESSOR; EXPRESSION; CANCER; METASTASIS; INHIBITION; ACTIVATION; RESISTANCE; PROGNOSIS;
D O I
10.1177/1010428317699129
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Pancreatic ductal adenocarcinoma is a highly malignant tumor with poor prognosis, and the biomarkers for the early diagnosis, targeting therapy, and prognosis are still not clinically available. This study investigated the expression of forkhead box P1 and forkhead box O3a proteins in human pancreatic ductal adenocarcinoma tumor tissues and pancreatic tissues with and without benign lesions using immunohistochemical staining. Results showed that the positive rates of forkhead box P1 and forkhead box O3a protein expression were significantly lower in pancreatic ductal adenocarcinoma tumors compared to peritumoral tissues, benign pancreatic tissues, and normal pancreatic tissues (p < 0.01). Pancreatic tissues with negative forkhead box P1 and forkhead box O3a protein expression exhibited dysplasia or intraepithelial neoplasia. The positive rates of forkhead box P1 and forkhead box O3a expression were significantly lower in cases with tumor mass >5 cm, lymph node metastasis, invasion to surrounding tissues and organs, and tumor-node-metastasis III + IV stage disease compared to cases with tumor mass 5 cm (p < 0.05), no lymph node metastasis (p < 0.001 and p = 0.001, respectively), no invasion (p = 0.003 and p = 0.004, respectively), and tumor-node-metastasis I or II stage disease (p < 0.05). Kaplan-Meier survival analysis showed that pancreatic ductal adenocarcinoma patients with negative forkhead box P1 and forkhead box O3a expression survived significantly shorter than patients with positive forkhead box P1 and forkhead box O3a expression (p = 0.000). Cox multivariate analysis revealed that negative forkhead box P1 and forkhead box O3a expression was an independent poor prognosis factor in pancreatic ductal adenocarcinoma patients. The area under the curve of a receiver operating characteristic curve was 0.642 for forkhead box P1 (95% confidence interval: 0.553-0.730) and 0.655 for forkhead box O3a (95% confidence interval: 0.6568-0.742). Loss of forkhead box P1 and forkhead box O3a protein expression is associated with carcinogenesis, progression, and poor prognosis in patients with pancreatic ductal adenocarcinomas.
引用
收藏
页数:9
相关论文
共 35 条
[1]   FoxOs at the crossroads of cellular metabolism, differentiation, and transformation [J].
Accili, D ;
Arden, KC .
CELL, 2004, 117 (04) :421-426
[2]   Multiple roles of FOXO transcription factors in mammalian cells point to multiple roles in cancer [J].
Arden, Karen C. .
EXPERIMENTAL GERONTOLOGY, 2006, 41 (08) :709-717
[3]   Strong expression of FOXP1 identifies a distinct subset of diffuse large B-cell lymphoma (DLBCL) patients with poor outcome [J].
Barrans, SL ;
Fenton, JAL ;
Banham, A ;
Owen, RG ;
Jack, AS .
BLOOD, 2004, 104 (09) :2933-2935
[4]   Potentially oncogenic B-cell activation-induced smaller isoforms of FOXP1 are highly expressed in the activated B cell-like subtype of DLBCL [J].
Brown, Philip J. ;
Ashe, Sally L. ;
Leich, Ellen ;
Burek, Christof ;
Barrans, Sharon ;
Fenton, James A. ;
Jack, Andrew S. ;
Pulford, Karen ;
Rosenwald, Andreas ;
Banham, Alison H. .
BLOOD, 2008, 111 (05) :2816-2824
[5]   FOXO3 expression during colorectal cancer progression: biomarker potential reflects a tumour suppressor role [J].
Bullock, M. D. ;
Bruce, A. ;
Sreekumar, R. ;
Curtis, N. ;
Cheung, T. ;
Reading, I. ;
Primrose, J. N. ;
Ottensmeier, C. ;
Packham, G. K. ;
Thomas, G. ;
Mirnezami, A. H. .
BRITISH JOURNAL OF CANCER, 2013, 109 (02) :387-394
[6]   FOXO transcription factors in cancer development and therapy [J].
de Brachene, Alexandra Coomans ;
Demoulin, Jean-Baptiste .
CELLULAR AND MOLECULAR LIFE SCIENCES, 2016, 73 (06) :1159-1172
[7]   Expression of FOXP1 and Colorectal Cancer Prognosis [J].
De Smedt, Linde ;
Palmans, Sofie ;
Govaere, Olivier ;
Moisse, Matthieu ;
Boeckx, Bram ;
De Hertogh, Gert ;
Prenen, Hans ;
Van Cutsem, Erik ;
Tejpar, Sabine ;
Tousseyn, Thomas ;
Sagaert, Xavier .
LABMEDICINE, 2015, 46 (04) :299-311
[8]   High Expression of FoxP1 Is Associated With Improved Survival in Patients With Non-Small Cell Lung Cancer [J].
Feng, Jian ;
Zhang, Xuesong ;
Zhu, Huijun ;
Wang, Xudong ;
Ni, Songshi ;
Huang, Jianfei .
AMERICAN JOURNAL OF CLINICAL PATHOLOGY, 2012, 138 (02) :230-235
[9]   FOXOs, cancer and regulation of apoptosis [J].
Fu, Z. ;
Tindall, D. J. .
ONCOGENE, 2008, 27 (16) :2312-2319
[10]   Loss of expression and nuclear/cytoplasmic localization of the FOXP1 forkhead transcription factor are common events in early endometrial cancer:: Relationship with estrogen receptors and HIF-1α expression [J].
Giatromanolaki, A ;
Koukourakis, MI ;
Sivridis, E ;
Gatter, KC ;
Harris, AL ;
Banham, AH .
MODERN PATHOLOGY, 2006, 19 (01) :9-16