Rho-GTPase activating-protein 18: a biomarker associated with good prognosis in invasive breast cancer

被引:15
作者
Aleskandarany, Mohammed A. [1 ,2 ]
Sonbul, Sultan [1 ]
Surridge, Rachel [1 ]
Mukherjee, Abhik [1 ]
Caldas, Carlos [3 ]
Diez-Rodriguez, Maria [1 ]
Ashankyty, Ibraheem [4 ]
Albrahim, Khalil I. [4 ]
Elmouna, Ahmed M. [4 ]
Aneja, Ritu [5 ]
Martin, Stewart G. [1 ]
Ellis, Ian O. [1 ]
Green, Andrew R. [1 ]
Rakha, Emad A. [1 ,2 ]
机构
[1] Univ Nottingham, Sch Med, Div Canc & Stem Cells, Nottingham NG5 1PB, England
[2] Menoufia Univ, Pathol Dept, Fac Med, Menoufyia 110532, Egypt
[3] Cambridge Res Inst, Canc Res UK, Cambridge CB 0RE, England
[4] Univ Hail, Mol Diagnost & Personalised Therapeut Unit, Hail 2440, Saudi Arabia
[5] Georgia State Univ, Dept Biol, POB 4010, Atlanta, GA 30303 USA
关键词
ARHGAP18; lymphovascular invasion; immunohistochemistry; breast cancer; prognosis; BLOOD-VESSEL INVASION; LYMPHOVASCULAR INVASION; ESTROGEN-RECEPTOR; MOTILITY;
D O I
10.1038/bjc.2017.261
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: The prognostic value of lymphovascular invasion (LVI) in breast cancer (BC) has been demonstrated in several independent studies. However, identification of driver molecules for LVI remains a challenging task. Large-scale transcriptomic profiling of histologically validated LVI can potentially identify genes that regulate LVI. Methods: Integrative bio-informatics analyses of the METABRIC study were performed utilising a subset of strictly defined LVI using histological and immunohistochemical (IHC) criteria. ARHGAP18 was among the top differentially expressed genes between LVI+ and LVI - BC with a 1.8-fold change. The prognostic impact of ARHGAP18 gene expression was assessed in the METABRIC data set (n = 1980) and externally validated using the online BC gene expression data sets utilising bc-GenExMiner v4.0 (n = 2016). Subsequently, ARHGAP18 protein expression was assessed on a large cohort of invasive BC (n = 959) with long-term follow-up using IHC. Results: Pooled analysis of ARHGAP18 mRNA expression showed that overexpression was associated with better outcome (P<0.001, hazard ratio (HR) = 0.82, 95% CI 0.75-0.90). ARHGAP18 protein was expressed in the cytoplasm and nuclei of the tumour cells and its expression was positively associated with good prognostic variables. Lack of cytoplasmic expression showed associations with LVI (P = 0.006), epithelial-mesenchymal transition and the HER+ subtype (P = 0.01). Loss of nuclear expression was associated with higher grade, HER2+ and high Ki67LI (P = 0.001). Cytoplasmic and nuclear expression showed a positive association with improved survival independent of other variables (P = 0.01, HR = 0.74, 95% CI 0.60-87). Conclusions: ARHGAP18 expression at transcriptomic and protein levels is associated with improved patients' outcomes whose deregulation may play a role in tumour progression and the development of LVI in BC. Further assessment of its potential therapeutic value in BC is warranted.
引用
收藏
页码:1176 / 1184
页数:9
相关论文
共 28 条
[1]   High-throughput protein expression analysis using tissue microarray technology of a large well-characterised series identifies biologically distinct classes of breast cancer confirming recent cDNA expression analyses [J].
Abd El-Rehim, DM ;
Ball, G ;
Pinder, SE ;
Rakha, E ;
Paish, C ;
Robertson, JFR ;
Macmillan, D ;
Blamey, RW ;
Ellis, IO .
INTERNATIONAL JOURNAL OF CANCER, 2005, 116 (03) :340-350
[2]   C-terminal Tensin-like (CTEN) is an oncogene which alters cell motility possibly through repression of E-cadherin in colorectal cancer [J].
Albasri, Abdulkader ;
Seth, Rashmi ;
Jackson, Darryl ;
Benhasouna, Ahmed ;
Crook, Simon ;
Nateri, Abdolrahman S. ;
Chapman, Roger ;
Ilyas, Mohammad .
JOURNAL OF PATHOLOGY, 2009, 218 (01) :57-65
[3]   Molecular Mechanisms Underlying Lymphovascular Invasion in Invasive Breast Cancer [J].
Aleskandarany, Mohammed A. ;
Sonbul, Sultan N. ;
Mukherjee, Abhik ;
Rakha, Emad A. .
PATHOBIOLOGY, 2015, 82 (3-4) :113-123
[4]   DIAGNOSTIC-TESTS-2 - PREDICTIVE VALUES .4. [J].
ALTMAN, DG ;
BLAND, JM .
BRITISH MEDICAL JOURNAL, 1994, 309 (6947) :102-102
[5]   ARHGAP21 Protein, a New Partner of α-Tubulin Involved in Cell-Cell Adhesion Formation and Essential for Epithelial-Mesenchymal Transition [J].
Barcellos, Karin S. A. ;
Bigarella, Carolina L. ;
Wagner, Mark V. ;
Vieira, Karla P. ;
Lazarini, Mariana ;
Langford, Peter R. ;
Machado-Neto, Joao A. ;
Call, Steven G. ;
Staley, Davis M. ;
Chung, Jarom Y. ;
Hansen, Marc D. ;
Saad, Sara T. O. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2013, 288 (04) :2179-2189
[6]   ARHGAP21 modulates FAK activity and impairs glioblastoma cell migration [J].
Bigarella, Carolina Louzao ;
Borges, Luciene ;
Costa, Fernando Ferreira ;
Olalla Saad, Sara Terezinha .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH, 2009, 1793 (05) :806-816
[7]  
Chang Garry H K, 2014, Small GTPases, V5, P1, DOI 10.4161/21541248.2014.975002
[8]  
Choi Seung-Hye, 2003, Breast J, V9, P153, DOI 10.1046/j.1524-4741.2003.09304.x
[9]   The genomic and transcriptomic architecture of 2,000 breast tumours reveals novel subgroups [J].
Curtis, Christina ;
Shah, Sohrab P. ;
Chin, Suet-Feung ;
Turashvili, Gulisa ;
Rueda, Oscar M. ;
Dunning, Mark J. ;
Speed, Doug ;
Lynch, Andy G. ;
Samarajiwa, Shamith ;
Yuan, Yinyin ;
Graef, Stefan ;
Ha, Gavin ;
Haffari, Gholamreza ;
Bashashati, Ali ;
Russell, Roslin ;
McKinney, Steven ;
Langerod, Anita ;
Green, Andrew ;
Provenzano, Elena ;
Wishart, Gordon ;
Pinder, Sarah ;
Watson, Peter ;
Markowetz, Florian ;
Murphy, Leigh ;
Ellis, Ian ;
Purushotham, Arnie ;
Borresen-Dale, Anne-Lise ;
Brenton, James D. ;
Tavare, Simon ;
Caldas, Carlos ;
Aparicio, Samuel .
NATURE, 2012, 486 (7403) :346-352
[10]   Re: Population-Based Study of Peritumoral Lymphovascular Invasion and Outcome Among Patients With Operable Breast Cancer [J].
Debled, Marc ;
de Mascarel, Isabelle ;
Brouste, Veronique ;
Mauriac, Louis ;
Macgrogan, Gaetan .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2010, 102 (04) :275-276