Expression and clinical significance of microRNA-126-3p in breast carcinomas with different immunohistochemical profiling
Liqin Li, Jing Li, Jinliang Ping, Huilian Huang, Jing Zhong, Licheng Dai
Abstract
Liqin Li, Jing Li, Jinliang Ping, Huilian Huang, Jing Zhong, Licheng Dai
Abstract
Objective To investigate the expression of microRNA (miRNA, miR)-126-3p in breast carcinomas with four different immunohistochemical profiling and their relevance to clinicopathologic features. Methods The expression of miR-126-3p was detected by real-time fluorescent quantitative polymerase chain reaction (FQ-PCR) in 67 paired frozen breast carcinomas tissues and further detected by TMA-ISH in 140 cases of formalin fixed paraffin-embedded (FFPE) breast carcinomas tissues. Results MiR-126-3p expression level was lower in carcinoma tissues than that in paired para-cancerous tissues, and lowest in triple-negative breast cancer (TNBC) immune phenotype without significant difference using FQ-PCR method. The results of TMA-ISH showed that miR-126-3p was mainly expressed in stroma of tumor tissue, and its expression level was higher in tumor tissue than that in breast fibroadenomas (χ2=21.48, P<0.01). Triple-negative breast cancers in stroma showed the lowest miR-126-3p expression level (high expression rate of 60%), and human epidermal growth factor receptor-2 (Her-2) over-expressed group showed the highest expression level (high expression rate of 91.3%) within four subtypes, which had the significant differences (χ2=6.26; P<0.05). Furthermore, strong miR-126-3p expression was significantly associated with Her-2 expression (χ2=5.73, P<0.05). Conclusion There was a difference in the miR-126-3p expression in breast tumor between different immune phenotypes, which may be used as a potential individual diagnostic and drug target for breast cancer patients. Key words: Breast carcinoma; MicroRNA-126-3p; Human epidermal growth factor receptor-2 over-expression
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Objective To investigate the expression of microRNA (miRNA, miR)-126-3p in breast carcinomas with four different immunohistochemical profiling and their relevance to clinicopathologic features. Methods The expression of miR-126-3p was detected by real-time fluorescent quantitative polymerase chain reaction (FQ-PCR) in 67 paired frozen breast carcinomas tissues and further detected by TMA-ISH in 140 cases of formalin fixed paraffin-embedded (FFPE) breast carcinomas tissues. Results MiR-126-3p expression level was lower in carcinoma tissues than that in paired para-cancerous tissues, and lowest in triple-negative breast cancer (TNBC) immune phenotype without significant difference using FQ-PCR method. The results of TMA-ISH showed that miR-126-3p was mainly expressed in stroma of tumor tissue, and its expression level was higher in tumor tissue than that in breast fibroadenomas (χ2=21.48, P<0.01). Triple-negative breast cancers in stroma showed the lowest miR-126-3p expression level (high expression rate of 60%), and human epidermal growth factor receptor-2 (Her-2) over-expressed group showed the highest expression level (high expression rate of 91.3%) within four subtypes, which had the significant differences (χ2=6.26; P<0.05). Furthermore, strong miR-126-3p expression was significantly associated with Her-2 expression (χ2=5.73, P<0.05). Conclusion There was a difference in the miR-126-3p expression in breast tumor between different immune phenotypes, which may be used as a potential individual diagnostic and drug target for breast cancer patients. Key words: Breast carcinoma; MicroRNA-126-3p; Human epidermal growth factor receptor-2 over-expression
Key concepts: Immunohistochemistry, Breast cancer, Breast carcinoma, Stroma, microRNA, Pathology, Clinical significance, Real-time polymerase chain reaction