Abstract PS17-35: B7-H3 and B7-H4 expression in triple-negative breast cancer subtypes detected by RNA in situ hybridization and immunohistochemistry: Association with clinicopathological features and T-cell infiltration

Author(s):  
Ji Shin Lee ◽  
Nah Ihm Kim ◽  
Min Ho Park
2021 ◽  
Vol 85 ◽  
pp. 104664
Author(s):  
Mohan Li ◽  
Kexin Zheng ◽  
Shiliang Ma ◽  
Pengpeng Hu ◽  
Bo Yuan ◽  
...  

2020 ◽  
pp. 23-31
Author(s):  
Anh Nguyen Phan Quynh ◽  
Thuan Dang Cong ◽  
Tien Nguyen Phuong Thao ◽  
Song Nguyen Tran Bao

Background: Breast cancer is the most frequent cause of cancer-related deaths among women worldwide. Molecular classification and the analysis of gene expression have been playing a pivotal role in deciding treatment therapy. The aim of study was to identify molecular surrogate subtypes of breast cancer by immunohistochemistry and Dual In Situ Hybridization, analysis of BCL11A gene expression was performed in molecular subtypes by RT-PCR and assessed the correlation between molecular subtypes and clinic-pathological characteristics. Materials and methods: Cross-sectional description study, tumor specimens from 138 patients were stained with Hematoxylin and Eosin to diagnosis, histopathological classification, stained with immunohistochemical markers ER, PR, HER2, Ki67 and Dual In Situ Hybridization (DISH) to classify molecular subtypes breast cancer. In which, RNA of 20 samples were extraction and performed by RT-PCR. Results: A significant association between breast carcinoma subtypes with histologic type (p=0.022) and grade (p=0.021). BCL11A was significantly down regulated in all molecular breast cancer subtypes especially in triple negative group. Conclusion: This study may help to understand pathological characteristics and the gene expression of difference breast cancer subtypes, contributing to the successful identification of therapeutic targets for breast cancer, especially triple negative group. Key words: Invasive breast carcinoma, molecular subtypes, histologic grade, Dual In Situ Hybridization (DISH), qRT-PCR


Cancers ◽  
2021 ◽  
Vol 13 (4) ◽  
pp. 765
Author(s):  
Florence Boissière-Michot ◽  
Ghita Chabab ◽  
Caroline Mollevi ◽  
Séverine Guiu ◽  
Evelyne Lopez-Crapez ◽  
...  

The prognostic impact of the different tumor-infiltrating lymphocyte (TIL) subpopulations in solid cancers is still debated. Here, we investigated the clinicopathological correlates and prognostic impact of TILs, particularly of γδ T cells, in 162 patients with triple-negative breast cancer (TNBC). A high γδ T cell density (>6.625 γδ T cells/mm2) was associated with younger age (p = 0.008), higher tumor histological grade (p = 0.002), adjuvant chemotherapy (p = 0.010), BRCA1 promoter methylation (p = 0.010), TIL density (p < 0.001), and PD-L1 (p < 0.001) and PD-1 expression (p = 0.040). In multivariate analyses, γδ T cell infiltration (cutoff = 6.625 γδ T cells/mm2) was an independent prognostic factor (5-year relapse-free survival: 63.3% vs. 89.8%, p = 0.027; 5-year overall survival: 73.8% vs. 89.9%, p = 0.031, for low vs. high infiltration). This prognostic impact varied according to the tumor PIK3CA mutational status. High γδ T cell infiltration was associated with better survival in patients with PIK3CA wild-type tumors, but the difference was not significant in the subgroup with PIK3CA-mutated tumors. Altogether, these data suggest that high γδ T cell infiltrate is correlated with immune infiltration and might represent a candidate prognostic tool in patients with TNBC.


Planta Medica ◽  
2015 ◽  
Vol 81 (11) ◽  
Author(s):  
AJ Robles ◽  
L Du ◽  
S Cai ◽  
RH Cichewicz ◽  
SL Mooberry

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