Association between RNF2+P-AKT expression in pretreatment biopsy specimens, and poor survival following radiotherapy in patients with esophageal squamous cell carcinoma

被引:4
作者
Li, Qiaofang [1 ,2 ]
Li, Shuguang [1 ]
Yang, Xingxiao [3 ]
Zhang, Xueyuan [1 ]
Song, Chunyang [1 ]
Zhu, Shuchai [1 ]
机构
[1] Hebei Med Univ, Hosp 4, Dept Radiat Oncol, 12 Jiankang Rd, Shijiazhuang 050011, Hebei, Peoples R China
[2] Hebei Gen Hosp, Dept Oncol, Shijiazhuang 050051, Hebei, Peoples R China
[3] Hebei Med Univ, Hosp 4, Dept Infect Dis, Shijiazhuang 050011, Hebei, Peoples R China
关键词
esophageal cancer; radiotherapy; Ring finger protein 2; phospho-protein kinase B; survival; prognostic factors; UBIQUITIN LIGASE; POLYCOMB PROTEINS; BREAST-CANCER; COMPLEX; BMI-1; PROLIFERATION; PROGNOSIS; RING1B; RADIORESISTANCE; ACTIVATION;
D O I
10.3892/ol.2019.10727
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The protein expression levels of Ring finger protein 2 (RNF2) and phosphor-protein kinase B (P-AKT) were determined in esophageal squamous cell carcinoma (ESCC) tissues, and the association between patient clinicopathological characteristics and survival time following definitive intensity-modulated radiotherapy was assessed. Cancerous biopsy tissues were collected from patients with ESCC at The Fourth Affiliated Hospital of Hebei Medical University between January 2010 and December 2013. Of these 99 cases, 83 were used to analyze the protein expression level of RNF2 (89.2% positive), 85 for P-AKT (65.9% positive) and 80 for RNF2+P-AKT protein expression levels (62.5% both positive). The expression levels of RNF2 protein in ESCC were associated with tumor volume (P=0.024), whilst those of P-AKT and RNF2+PAKT were associated with sex (P=0.041 and P=0.003, respectively). There were no significant differences in overall survival (OS) or progression-free survival (PFS) rate between the RNF2(-) and the RNF2(+-+++) groups (P=0.134 and P=0.366, respectively), or between the P-AKT(-) group and P-AKT(+-+++) group (P=0.468; P=0.580, respectively). The 1-, 3- and 5-year OS rates were 68.0, 28.0, and 20.0%, and 86.7, 53.3, and 31.1%, in the RNF2/P-AKT(+) group and Other group, respectively (chi(2)=4.205; P=0.040). Multivariate analysis revealed that age, T stage and RNF2+P-AKT expression were independent prognostic factors for ESCC (P=0.010, P=0.008 and P=0.010, respectively). The expression of RNF2+P-AKT combined was an independent prognostic factor affecting survival rate, and therefore presents a potential prognostic indicator for patients with ESCC, treated with definitive radiotherapy.
引用
收藏
页码:3734 / 3742
页数:9
相关论文
共 40 条
[1]   The polycomb protein Ring1B generates self atypical mixed ubiquitin chains required for its in vitro histone H2A ligase activity [J].
Ben-Saadon, Ronen ;
Zaaroor, Daphna ;
Ziv, Tamar ;
Ciechanover, Aaron .
MOLECULAR CELL, 2006, 24 (05) :701-711
[2]   Recognition of UbcH5c and the nucleosome by the Bmi1/Ring1b ubiquitin ligase complex [J].
Bentley, Matthew L. ;
Corn, Jacob E. ;
Dong, Ken C. ;
Phung, Qui ;
Cheung, Tommy K. ;
Cochran, Andrea G. .
EMBO JOURNAL, 2011, 30 (16) :3285-3297
[3]   The Polycomb group protein RING1B is overexpressed in ductal breast carcinoma and is required to sustain FAK steady state levels in breast cancer epithelial cells [J].
Bosch, Almudena ;
Panoutsopoulou, Konstantina ;
Maria Corominas, Josep ;
Gimeno, Ramon ;
Moreno-Bueno, Gema ;
Martin-Caballero, Juan ;
Morales, Saleta ;
Lobato, Tania ;
Martinez-Romero, Carles ;
Farias, Eduardo F. ;
Mayol, Xavier ;
Cano, Amparo ;
Hernandez-Munoz, Inmaculada .
ONCOTARGET, 2014, 5 (08) :2065-2076
[4]   Structure and E3-ligase activity of the Ring-Ring complex of polycomb proteins Bmi1 and Ring1b [J].
Buchwald, Gretel ;
van der Stoop, Petra ;
Weichenrieder, Oliver ;
Perrakis, Anastassis ;
van Lohuizen, Maarten ;
Sixma, Titia K. .
EMBO JOURNAL, 2006, 25 (11) :2465-2474
[5]   Activation of the PI3-K/AKT pathway and implications for radioresistance mechanisms in head and neck cancer [J].
Bussink, Johan ;
van der Kogel, Albert J. ;
Kaanders, Johannes H. A. M. .
LANCET ONCOLOGY, 2008, 9 (03) :288-296
[6]   Snail Recruits Ring1B to Mediate Transcriptional Repression and Cell Migration in Pancreatic Cancer Cells [J].
Chen, Jiangzhi ;
Xu, Hong ;
Zou, Xiuqun ;
Wang, Jiamin ;
Zhu, Yi ;
Chen, Hao ;
Shen, Baiyong ;
Deng, Xiaxing ;
Zhou, Aiwu ;
Chin, Y. Eugene ;
Rauscher, Frank J., III ;
Peng, Chenghong ;
Hou, Zhaoyuan .
CANCER RESEARCH, 2014, 74 (16) :4353-4363
[7]   H2AK119Ub1 and H3K27Me3 in molecular staging for survival prediction of patients with pancreatic ductal adenocarcinoma [J].
Chen, Shi ;
Chen, Jiangzhi ;
Zhan, Qian ;
Zhu, Yi ;
Chen, Hao ;
Deng, Xiaxing ;
Hou, Zhaoyuan ;
Shen, Baiyong ;
Chen, Yanling ;
Peng, Chenghong .
ONCOTARGET, 2014, 5 (21) :10421-10433
[8]   PKB/Akt promotes DSB repair in cancer cells through upregulating Mre11 expression following ionizing radiation [J].
Deng, R. ;
Tang, J. ;
Ma, J-G ;
Chen, S-P ;
Xia, L-P ;
Zhou, W-J ;
Li, D-D ;
Feng, G-K ;
Zeng, Y-X ;
Zhu, X-F .
ONCOGENE, 2011, 30 (08) :944-955
[9]  
Edge SB., 2009, AJCC CANC STAGING MA, V7th, P103
[10]   The Global Burden of Cancer 2013 Global Burden of Disease Cancer Collaboration [J].
Fitzmaurice, Christina ;
Dicker, Daniel ;
Pain, Amanda ;
Hamavid, Hannah ;
Moradi-Lakeh, Maziar ;
Maclntyre, Michael F. ;
Allen, Christine ;
Hansen, Gillian ;
Woodbrook, Rachel ;
Wolfe, Charles ;
Hamadeh, Randah R. ;
Moore, Ami ;
Werdecker, Andrea ;
Gessner, Bradford D. ;
Te Ao, Braden ;
McMahon, Brian ;
Karimkhani, Chante ;
Yu, Chuanhua ;
Cooke, Graham S. ;
Schwebel, David C. ;
Carpenter, David O. ;
Pereira, David M. ;
Nash, Denis ;
Kazi, Dhruv S. ;
De Leo, Diego ;
Plass, Dietrich ;
Ukwaja, Kingsley N. ;
Thurston, George D. ;
Jin, Kim Yun ;
Simard, Edgar P. ;
Mills, Edward ;
Park, Eun-Kee ;
Catala-Lopez, Ferran ;
DeVeber, Gabrielle ;
Gotay, Carolyn ;
Khan, Gulfaraz ;
Hosgood, H. Dean, III ;
Santos, Itamar S. ;
Leasher, Janet L. ;
Singh, Jasvinder ;
Leigh, James ;
Jonas, Jost B. ;
Sanabria, Juan ;
Beardsley, Justin ;
Jacobsen, Kathryn H. ;
Takahashi, Ken ;
Franklin, Richard C. ;
Ronfani, Luca ;
Montico, Marcella ;
Naldi, Luigi .
JAMA ONCOLOGY, 2015, 1 (04) :505-527