Factor-inhibiting hypoxia-inducible factor expression in patients with high-risk locally advanced renal cell carcinoma and its relationship with tumor progression

被引:5
|
作者
Deng, Shi [1 ]
Zhang, Peng [1 ]
Zeng, Hao [1 ]
Wang, Wei [2 ]
Jin, Tao [1 ]
Wang, Jia [1 ]
Dong, Qiang [1 ]
机构
[1] Sichuan Univ, West China Hosp, Dept Urol, Chengdu 610041, Peoples R China
[2] West China Second Univ Hosp, Dept Pathol, Chengdu, Peoples R China
来源
KAOHSIUNG JOURNAL OF MEDICAL SCIENCES | 2014年 / 30卷 / 01期
关键词
Adjuvant therapy; Factor-inhibiting hypoxia-inducible factor; Locally advanced renal cell carcinoma; ENDOTHELIAL GROWTH-FACTOR; FACTOR; 1-ALPHA; BREAST-CANCER; SURVIVAL; THERAPY; HIF; FIH; OVEREXPRESSION; HYDROXYLASE; DISTINCT;
D O I
10.1016/j.kjms.2013.07.001
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Hypoxia-inducible factor (HIF) plays an important role in renal cell carcinoma (RCC) associated with angiogenesis. Factor-inhibiting HIF (FIH), which is the upstream mediator protein of HIF, is receiving more attention today. In the present study, the role of FIH expression in high-risk locally advanced renal cell carcinoma (LARCC) was explored. Eighty-eight high-risk LARCC cases were divided into two groups based on their prognosis. Using immunohistochemical staining, the correlations of FIH expression along with clinicopathological factors, progression-free survival (PFS), and overall survival (OS) were analyzed. FIH was mainly located in the cytoplasm (34/88) and nucleus (31/88) of the renal tumor cell. Nuclear negative expression or cytoplasmic positive expression of FIH were associated with an increased risk of disease progression (p = 0.007 and p < 0.001, respectively) and worse OS (p = 0.020 and p = 0.008, respectively). Using the group with nuclear and cytoplasmic FIH negative expression as reference, further stratified analysis found that the exclusive nuclear FIH expression group had a better PFS and OS [hazard ratio (HR) = 0.153, p = 0.07 and HR = 0, p = 0.961, respectively], and the exclusive cytoplasmic FIH positive group experienced the worst PFS and OS (HR = 2.876, p = 0.005 and HR = 2.799, p = 0.034, respectively). In addition, nuclear negative expression of FIH was associated with a significant negative predictive value for the effect of interferon-alpha (IFN-alpha) on PFS (p = 0.045). The nuclear negative and cytoplasmic positive expressions of FIH were identified not only as risk factors for disease progression in high-risk LARCC postoperative patients, but also to be associated with poor OS. Furthermore, the nuclear negative expression of FIH may be a promising biomarker for postoperative adjuvant therapy. Copyright (C) 2013, Kaohsiung Medical University. Published by Elsevier Taiwan LLC. All rights reserved.
引用
收藏
页码:12 / 19
页数:8
相关论文
共 50 条
  • [41] Over-expression of hypoxia-inducible factor 1 alpha in ovarian clear cell carcinoma
    Lee, Sunyoung
    Garner, Elizabeth I. O.
    Welch, William R.
    Berkowitz, Ross S.
    Mok, Samuel C.
    GYNECOLOGIC ONCOLOGY, 2007, 106 (02) : 311 - 317
  • [42] Vasculogenic mimicry and hypoxia-inducible factor-1α expression in cervical squamous cell carcinoma
    Zhou, T. J.
    Huang, X. H.
    Gong, L.
    Xiang, L.
    GENETICS AND MOLECULAR RESEARCH, 2016, 15 (01)
  • [43] Expression of hypoxia-inducing protein 2 and hypoxia-inducible factor-1 in acquired renal cystic disease associated with renal cell carcinoma
    Konda, Ryuichiro
    Sugiura, Jun
    Obara, Wataru
    Togashi, Akira
    Katagiri, Toyomasa
    Fujioka, Tomoaki
    NEPHROLOGY DIALYSIS TRANSPLANTATION, 2006, 21 : 371 - 372
  • [44] Prognostic significance of hypoxia inducible factor-1 expression in patients with clear cell renal cell carcinoma
    Wu, Shuiqing
    Jiang, Fen
    Wu, Hongtao
    Wang, Yinhuai
    Xu, Ran
    Cao, Jian
    Lu, Qiong
    Zhu, Xuan
    Zhong, Zhaohui
    Zhao, Xiaokun
    MOLECULAR MEDICINE REPORTS, 2018, 17 (03) : 4846 - 4852
  • [45] Targeting myeloid-derived suppressor cells by inhibiting hypoxia-inducible factor 1α could improve tumor progression
    Xu, Qiying
    Liu, Huifang
    Song, Xiaoyan
    Wuren, Tana
    Ge, Ri-li
    ANNALS OF MEDICINE AND SURGERY, 2024, 86 (08): : 4449 - 4455
  • [46] Excisanin A suppresses proliferation by inhibiting hypoxia-inducible factor-1α expression in human hepatocellular carcinoma cells
    Han, Li Zhuo
    Jiang, Changgao
    Mi, Chunliu
    Wang, Ke Si
    Zuo, Hong Xiang
    Wang, Zhe
    Li, Ming Yue
    Zhang, Zhi Hong
    Jin, Xuejun
    TROPICAL JOURNAL OF PHARMACEUTICAL RESEARCH, 2020, 19 (12) : 2483 - 2489
  • [47] Over expression of hypoxia-inducible protein 2, hypoxia-inducible factor-1α and nuclear factor κB is putatively involved in acquired renal cyst formation and subsequent tumor transformation in patients with end stage renal failure
    Konda, Ryuichiro
    Sugimura, Jun
    Sohma, Fumihiko
    Katagiri, Toyomasa
    Nakamura, Yusuke
    Fujioka, Tomoaki
    JOURNAL OF UROLOGY, 2008, 180 (02): : 481 - 485
  • [48] Hypoxia-inducible factor 1 alpha in oral squamous cell carcinoma and its relation to prognosis
    Uehara, Masataka
    Sano, Kazuo
    Ikeda, Hisazumi
    Nonaka, Mihoko
    Asahina, Izumi
    ORAL ONCOLOGY, 2009, 45 (03) : 241 - 246
  • [49] Nuclear PROX1 is Associated with Hypoxia-Inducible Factor 1α Expression and Cancer Progression in Esophageal Squamous Cell Carcinoma
    Takehiko Yokobori
    Pinjie Bao
    Minoru Fukuchi
    Bolag Altan
    Daigo Ozawa
    Susumu Rokudai
    Tuya Bai
    Yuji Kumakura
    Hiroaki Honjo
    Keigo Hara
    Makoto Sakai
    Makoto Sohda
    Tatsuya Miyazaki
    Munenori Ide
    Masahiko Nishiyama
    Tetsunari Oyama
    Hiroyuki Kuwano
    Annals of Surgical Oncology, 2015, 22 : 1566 - 1573
  • [50] Nuclear PROX1 is Associated with Hypoxia-Inducible Factor 1α Expression and Cancer Progression in Esophageal Squamous Cell Carcinoma
    Yokobori, Takehiko
    Bao, Pinjie
    Fukuchi, Minoru
    Altan, Bolag
    Ozawa, Daigo
    Rokudai, Susumu
    Bai, Tuya
    Kumakura, Yuji
    Honjo, Hiroaki
    Hara, Keigo
    Sakai, Makoto
    Sohda, Makoto
    Miyazaki, Tatsuya
    Ide, Munenori
    Nishiyama, Masahiko
    Oyama, Tetsunari
    Kuwano, Hiroyuki
    ANNALS OF SURGICAL ONCOLOGY, 2015, 22 : S1566 - S1573