MAPK, NFκB, and VEGF signaling pathways regulate breast cancer liver metastasis

被引:13
作者
Chen, Xinhua [1 ,2 ]
Zheng, Zhihong [3 ]
Chen, Limin [1 ,2 ]
Zheng, Hongyu [1 ,2 ]
机构
[1] Fujian Canc Hosp, Dept Med Oncol, Fuzhou, Fujian, Peoples R China
[2] Fujian Med Univ, Canc Hosp, Fuzhou, Fujian, Peoples R China
[3] Fujian Med Univ, Union Hosp, Dept Hematol, Fuzhou, Fujian, Peoples R China
关键词
breast cancer; metastasis; liver; microarray; interaction network; TO-MESENCHYMAL TRANSITION; PROGNOSTIC-FACTORS; 1ST RECURRENCE; PLATELETS; BEVACIZUMAB; PRINCIPLES; SURVIVAL;
D O I
10.18632/oncotarget.20843
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
In this study, we investigated the molecular pathways regulating breast cancer liver metastasis. We identified 48 differentially expressed genes (4 upregulated and 44 downregulated) by analyzing microarray dataset GSE62598 from Gene Expression Omnibus (GEO). We constructed a genetic interaction network with 84 nodes and 237 edges using the String consortium database. The network was reliably robust with a clustering coefficient (cc) of 0.598 and protein-protein interaction (PPI) enrichment p value of zero. Using the Gene Ontology and Kyoto Encyclopedia of Genes and Genomes databases, we identified MAPK, NF kappa B and VEGF signaling pathways as the most critical pathways regulating breast cancer liver metastasis. These results indicate that the distinct breast cancer metastatic stages, including dissemination from the primary breast tumor, transit through the vasculature, and survival and proliferation in the liver, are regulated by the MAPK, NF kappa B, and VEGF signaling pathways.
引用
收藏
页码:101452 / 101460
页数:9
相关论文
共 28 条
[1]   Is liver resection justified for patients with hepatic metastases from breast cancer? [J].
Adam, Rene ;
Aloia, Thomas ;
Krissat, Jinane ;
Bralet, Marie-Pierre ;
Paule, Bernard ;
Giacchetti, Sylvie ;
Delvart, Valerie ;
Azoulay, Daniel ;
Bismuth, Henri ;
Castaing, Denis .
ANNALS OF SURGERY, 2006, 244 (06) :897-908
[2]   SURVIVAL FROM 1ST RECURRENCE - RELATIVE IMPORTANCE OF PROGNOSTIC FACTORS IN 1,015 BREAST-CANCER PATIENTS [J].
CLARK, GM ;
SLEDGE, GW ;
OSBORNE, CK ;
MCGUIRE, WL .
JOURNAL OF CLINICAL ONCOLOGY, 1987, 5 (01) :55-61
[3]   RSK Is a Principal Effector of the RAS-ERK Pathway for Eliciting a Coordinate Promotile/Invasive Gene Program and Phenotype in Epithelial Cells [J].
Doehn, Ulrik ;
Hauge, Camilla ;
Frank, Scott R. ;
Jensen, Claus J. ;
Duda, Katarzyna ;
Nielsen, Jakob V. ;
Cohen, Michael S. ;
Johansen, Jens V. ;
Winther, Benny R. ;
Lund, Leif R. ;
Winther, Ole ;
Taunton, Jack ;
Hansen, Steen H. ;
Froedin, Morten .
MOLECULAR CELL, 2009, 35 (04) :511-522
[4]   KIAA0101 is associated with human renal cell carcinoma proliferation and migration induced by erythropoietin [J].
Fan, Shengjun ;
Li, Xin ;
Tie, Lu ;
Pan, Yan ;
Li, Xuejun .
ONCOTARGET, 2016, 7 (12) :13520-13537
[5]   The biology of vascular endothelial growth factor [J].
Ferrara, N ;
DavisSmyth, T .
ENDOCRINE REVIEWS, 1997, 18 (01) :4-25
[6]   Epithelial-to-mesenchymal transition is not required for lung metastasis but contributes to chemoresistance [J].
Fischer, Kari R. ;
Durrans, Anna ;
Lee, Sharrell ;
Sheng, Jianting ;
Li, Fuhai ;
Wong, Stephen T. C. ;
Choi, Hyejin ;
El Rayes, Tina ;
Ryu, Seongho ;
Troeger, Juliane ;
Schwabe, Robert F. ;
Vahdat, Linda T. ;
Altorki, Nasser K. ;
Mittal, Vivek ;
Gao, Dingcheng .
NATURE, 2015, 527 (7579) :472-+
[7]   Breast and cervical cancer in 187 countries between 1980 and 2010: a systematic analysis [J].
Forouzanfar, Mohammad H. ;
Foreman, Kyle J. ;
Delossantos, Allyne M. ;
Lozano, Rafael ;
Lopez, Alan D. ;
Murray, Christopher J. L. ;
Naghavi, Mohsen .
LANCET, 2011, 378 (9801) :1461-1484
[8]   Platelets at the interface of thrombosis, inflammation, and cancer [J].
Franco, Aime T. ;
Corken, Adam ;
Ware, Jerry .
BLOOD, 2015, 126 (05) :582-588
[9]   Contribution of platelets to tumour metastasis [J].
Gay, Laurie J. ;
Felding-Habermann, Brunhilde .
NATURE REVIEWS CANCER, 2011, 11 (02) :123-134
[10]   Shared principles in NF-κB signaling [J].
Hayden, Matthew S. ;
Ghosh, Sankar .
CELL, 2008, 132 (03) :344-362