COX-2 promotes metastasis and predicts prognosis in gastric cancer via regulating mTOR

被引:10
作者
Xiang, Liangliang [1 ,2 ]
Wang, Weimin [1 ,2 ,3 ]
Zhou, Zhen [1 ,2 ]
Lv, Mengying [1 ,2 ]
Tao, Li [1 ,2 ]
Ni, Tengyang [1 ,2 ]
Deng, Jianliang [3 ]
Masatara, Sunagawa [4 ]
Liu, Yanqing [1 ,2 ,3 ]
Zhou, Yan [1 ,2 ,3 ]
机构
[1] Yangzhou Univ, Inst Translat Med, Coll Med, Yangzhou 225001, Jiangsu, Peoples R China
[2] State Adm Tradit Chinese Med, Key Lab Syndrome Differentiat & Treatment Gastr C, Tradit Chinese Med Adm, Yangzhou 225001, Jiangsu, Peoples R China
[3] Yangzhou Univ, Dept Oncol, Yixing Hosp, Coll Med, Yixing 214200, Jiangsu, Peoples R China
[4] Showa Univ, Sch Med, Dept Physiol, Tokyo 142, Japan
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
COX-2; gastric cancer; metastasis; mTOR; prognosis; METABOLISM; TARGET; INFLAMMATION; CULLIN1; MARKER;
D O I
10.2217/bmm-2019-0357
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
Aim: Gastric cancer (GC) is one of the most common malignant tumors in the world. It is important to find accurate and reliable biomarkers in order to decrease whole morbidity and mortality. Results: We examined the expression of COX-2 and mTOR on GC tissue microarrays by immunohistochemistry. Multi-variate COX regression analysis showed that the expression of COX-2 or mTOR was an independent factor in the prognosis of GC patients. In addition, COX-2 and mTOR had the potentially synergistic effect on predicting the prognosis of GC. Conclusion: The combined expression of COX-2 and mTOR could serve as efficient prognostic indicators and COX-2 could suppress GC metastasis via regulating mTOR.
引用
收藏
页码:421 / 432
页数:12
相关论文
共 27 条
[1]   Cullin1 is a novel marker of poor prognosis and a potential therapeutic target in human breast cancer [J].
Bai, J. ;
Yong, H. M. ;
Chen, F. F. ;
Mei, P. J. ;
Liu, H. ;
Li, C. ;
Pan, Z. Q. ;
Wu, Y. P. ;
Zheng, J. N. .
ANNALS OF ONCOLOGY, 2013, 24 (08) :2016-2022
[2]   The hairless mouse in skin research [J].
Benavides, Fernando ;
Oberyszyn, Tatiana M. ;
VanBuskirk, Anne M. ;
Reeve, Vivienne E. ;
Kusewitt, Donna F. .
JOURNAL OF DERMATOLOGICAL SCIENCE, 2009, 53 (01) :10-18
[3]   Role of LKB1-CRTC1 on Glycosylated COX-2 and Response to COX-2 Inhibition in Lung Cancer [J].
Cao, Chunxia ;
Gao, Ruli ;
Zhang, Min ;
Amelio, Antonio L. ;
Fallahi, Mohammad ;
Chen, Zirong ;
Gu, Yumei ;
Hu, Chengbin ;
Welsh, Eric A. ;
Engel, Brienne E. ;
Haura, Eric B. ;
Cress, W. Douglas ;
Wu, Lizi ;
Zajac-Kaye, Maria ;
Kaye, Frederic J. .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2015, 107 (01)
[4]   Cyclo-oxygenase 2: a pharmacological target for the prevention of cancer [J].
Dannenberg, AJ ;
Altorki, NK ;
Boyle, JO ;
Dang, C ;
Howe, LR ;
Weksler, BB ;
Subbararnaiah, K .
LANCET ONCOLOGY, 2001, 2 (09) :544-551
[5]   mTOR and Tumor Cachexia [J].
Duval, Adrian P. ;
Jeanneret, Cheryl ;
Santoro, Tania ;
Dormond, Olivier .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2018, 19 (08)
[6]   Cancer incidence and mortality among young adults aged 20-39 years worldwide in 2012: a population-based study [J].
Fidler, Miranda M. ;
Gupta, Sumit ;
Soerjomataram, Isabelle ;
Ferlay, Jacques ;
Steliarova-Foucher, Eva ;
Bray, Freddie .
LANCET ONCOLOGY, 2017, 18 (12) :1579-1589
[7]   Defining the role of mTOR in cancer [J].
Guertin, David A. ;
Sabatini, David M. .
CANCER CELL, 2007, 12 (01) :9-22
[8]   mTOR signaling in osteosarcoma: Oncogenesis and therapeutic aspects (Review) [J].
Hu, Kai ;
Dai, Hai-Bo ;
Qiu, Zhi-Long .
ONCOLOGY REPORTS, 2016, 36 (03) :1219-1225
[9]   Japanese gastric cancer treatment guidelines 2014 (ver. 4) [J].
Japanese Gastric Cancer Association .
GASTRIC CANCER, 2017, 20 (01) :1-19
[10]   Cell-type-specific roles for COX-2 in UVB-induced skin cancer [J].
Jiao, Jing ;
Mikulec, Carol ;
Ishikawa, Tomo-o ;
Magyar, Clara ;
Dumlao, Darren S. ;
Dennis, Edward A. ;
Fischer, Susan M. ;
Herschman, Harvey .
CARCINOGENESIS, 2014, 35 (06) :1310-1319