| 
                                                    Study of androgen receptor as a quadruple marker in breast carcinoma
                                                 | 
                                             
                                            
                                                
                                                     
                                                 | 
                                             
                                            
                                                
                                                    
                                                        
                                                            | Author:
                                                             | 
                                                            
                                                                TYAGI KISHOR, PRACHI PALSODKAR, PRACHI PALSODKAR, VAGHA SUNIT, HIWALE KISHORE MADHAVRAO
                                                             | 
                                                         
                                                        
                                                            | Abstract:
                                                             | 
                                                            
                                                                Background: Breast carcinoma  is second largest cause of tumor/cancer in the world. Breast carcinoma can be de?ned according to absence/presence of expression of oestrogen, progesterone & HER-2 receptor. Absence of all of three receptor called as Triple negative breast carcinoma (TNBC). Four main TNBC subtypes have been de?ned, Basal 1 & 2, LAR (Luminal androgen receptor) & Mesenchymal. Luminal androgen receptor depends on Androgen Receptor signaling pathway and most sensitive to AR-antagonists. Androgen receptors plays crucial role in the treatment of Carcinoma Breast, mostly used in Tamoxifen resistant and Triple negative breast carcinoma are Androgen Receptor Antagonist
Objectives: Compare of AR status with ER,PR, and Her2.
Methodology: Slide of newly diagnosed patients of breast carcinoma stained by H  and E stain and immunohistochemical stain(ER,PR,Her2,AR) will be studied.
Results: Result would be undertaken in spss softwere.
Conclusion: The conclusion will be based on findings of the study of protocol. 
                                                             | 
                                                         
                                                        
                                                            | Keyword:
                                                             | 
                                                            
                                                                Carcinoma Breast, ER, AR, PR, HER2, TNBC, Breast carcinoma Progesterone receptor, Estrogen receptor, Human epidermal growth receptor 2, Triple negative breast carcinoma
                                                             | 
                                                         
                                                        
					| EOI:
                                                             | 
					
                                                                -
                                                             | 
				 
				
                                                        
					| DOI:
                                                             | 
					
                                                                https://doi.org/10.31838/ijpr/2019.11.01.208
                                                             | 
				 
				
                                                        
                                                            | Download:
                                                             | 
                                                            
                                                                Request For Article
                                                                
                                                                
                                                             | 
                                                         
                                                     
                                                 | 
                                             
                                         
                                     |