PRR14 is an independent predictor of poor prognosis in resected non-small cell lung cancer patients

被引:0
作者
Yu, He [1 ]
Zhou, Ping [1 ]
Li, Dan [1 ]
Liu, Dan [1 ]
Li, Weimin [1 ]
机构
[1] Sichuan Univ, West China Hosp, Dept Resp Med, Chengdu 610041, Sichuan Provinc, Peoples R China
来源
INTERNATIONAL JOURNAL OF CLINICAL AND EXPERIMENTAL PATHOLOGY | 2017年 / 10卷 / 06期
关键词
PRR14; non-small cell lung cancer; prognosis; PROLINE-RICH MOTIFS; PHOSPHOINOSITIDE; 3-KINASE; CYCLE PROGRESSION; PATHWAY; PROLIFERATION; STATISTICS; ROLES; PYK2;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Recently PRR14 has been found to be involved in lung carcinogenesis, and the high-level mRNA expression of PRR14 is associated with worse survival overall in lung cancers. However, there are few studies focused on the problem. Therefore, we evaluated the expression of PRR14 by immmunohistochemistry and the associations with prognosis in resected non-small cell lung cancer (NSCLC) patients. Totally, a number of 199 patients were enrolled in our study. We found that PRR14 was nuclear staining in lung tumor samples and positive expression in 95 out of 199 NSCLC patients (47.7%). PRR14 expression was significantly associated with gender, smoking history, histological type, lymph node infiltration in resected NSCLC patients (all P<0.05). Patients with PRR14-positive expression had worse 5-year survival (P=0.002) and shorter progression-free survival (PFS, P= 0.006) than patients with PRR14-negative expression by univariate analysis. More interestingly, the multivariate analysis also suggested that PRR14 positive expression was significantly related to poorer OS and PFS (all P<0.05), independent of the clinicopathological features of NSCLC patients. Thus, our study indicated that PRR14 was an independent predictor of unfavorable prognosis in resected NSCLC patients and may serve as a potential target.
引用
收藏
页码:6735 / 6742
页数:8
相关论文
共 33 条
  • [1] Phosphoinositide 3-kinase is required for human adipocyte differentiation in culture
    Aubin, D
    Gagnon, A
    Sorisky, A
    [J]. INTERNATIONAL JOURNAL OF OBESITY, 2005, 29 (08) : 1006 - 1009
  • [2] Recognition of proline-rich motifs by protein-protein-interaction domains
    Ball, LJ
    Kühne, R
    Schneider-Mergener, J
    Oschkinat, H
    [J]. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2005, 44 (19) : 2852 - 2869
  • [3] The PTEN-PI3K pathway: of feedbacks and cross-talks
    Carracedo, A.
    Pandolfi, P. P.
    [J]. ONCOGENE, 2008, 27 (41) : 5527 - 5541
  • [4] Metastasis: recent discoveries and novel treatment strategies
    Eccles, Suzanne A.
    Welch, Danny R.
    [J]. LANCET, 2007, 369 (9574) : 1742 - 1757
  • [5] The American Joint Committee on Cancer: the 7th Edition of the AJCC Cancer Staging Manual and the Future of TNM
    Edge, Stephen B.
    Compton, Carolyn C.
    [J]. ANNALS OF SURGICAL ONCOLOGY, 2010, 17 (06) : 1471 - 1474
  • [6] New response evaluation criteria in solid tumours: Revised RECIST guideline (version 1.1)
    Eisenhauer, E. A.
    Therasse, P.
    Bogaerts, J.
    Schwartz, L. H.
    Sargent, D.
    Ford, R.
    Dancey, J.
    Arbuck, S.
    Gwyther, S.
    Mooney, M.
    Rubinstein, L.
    Shankar, L.
    Dodd, L.
    Kaplan, R.
    Lacombe, D.
    Verweij, J.
    [J]. EUROPEAN JOURNAL OF CANCER, 2009, 45 (02) : 228 - 247
  • [7] Role of PI3K/AKT/mTOR signaling in the cell cycle progression of human prostate cancer
    Gao, N
    Zhang, Z
    Jiang, BH
    Shi, XL
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2003, 310 (04) : 1124 - 1132
  • [8] G1 cell cycle progression and the expression of G1 cyclins are regulated by PI3K/AKT/mTOR/p70S6K1 signaling in human ovarian cancer cells
    Gao, N
    Flynn, DC
    Zhang, Z
    Zhong, XS
    Walker, V
    Liu, KJ
    Shi, XL
    Jiang, BH
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 2004, 287 (02): : C281 - C291
  • [9] Gedaly R, 2010, ANTICANCER RES, V30, P4951
  • [10] Phosphoinositide 3-kinase activates Rac by entering in a complex with Eps8, Abi1, and Sos-1
    Innocenti, M
    Frittoli, E
    Ponzanelli, I
    Falck, JR
    Brachmann, SM
    Di Fiore, PP
    Scita, G
    [J]. JOURNAL OF CELL BIOLOGY, 2003, 160 (01) : 17 - 23