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1.
Chinese Journal of Oncology ; (12): 165-169, 2023.
Artigo em Chinês | WPRIM | ID: wpr-969820

RESUMO

Objective: To observe the clinical pathology features, and immune microenvironment of HER-2 intratumoral heterogeneity breast cancer. Methods: Thirty cases of HER-2 intratumoral heterogeneous breast cancer were retrospectively analyzed in Tianjin Medical University Cancer Institute and Hospital from November 2017 to June 2020. HER-2 expression was detected by immunohistochemistry and verified by dual color silver-enhanced in-situ hybridization (D-SISH). HER-2 intratumoral positive and negative regions were divided. The pathological characteristics, subtype, and the level of tumor infiltrating lymphocytes (TILs) and the expression of programmed cell death-ligand 1 (PD-L1) were evaluated respectively. Results: The proportion of HER-2 positive cells of the breast cancer ranged from 10% to 90%. The pathological type was mainly invasive non-special typecarcinoma. Six cases presented different pathological types between HER-2 positive and negative regions. The HER-2-positive areas included 2 cases of carcinoma with apocrine differentiation, and the negative areas included 2 cases of invasive micropapillary carcinoma, 1 case of invasive papillary carcinoma, and 1 case of carcinoma with apocrine differentiation. In HER-2 positive regions, 17 cases were Luminal B and 13 cases were HER-2 overexpressed types. There were 22 cases of Luminal B and 8 cases of triple negative tumors in the HER-2 negative areas. The levels of TILs in HER-2 positive and negative areas accounted for 53.3% (16/30) and 26.7% (8/30), respectively, with a statistically significant difference (P=0.035). The positive expression of PD-L1 in HER-2 positive area and HER-2 negative area were 6 cases and 9 cases, respectively. Among 8 cases with HER-2 negative regions containing triple negative components, 4 cases were positive for PD-L1 expression. Conclusions: In the case of HER-2 intratumoral heterogeneity, it is necessary to pay attention to both HER-2 positive and negative regions, and evaluate subtype separately as far as possible. For HER-2 intratumoral heterogeneous breast cancer containing triple negative components, the treatment mode can be optimized by refining the intratumoral expression of PD-L1.


Assuntos
Humanos , Feminino , Neoplasias da Mama/patologia , Estudos Retrospectivos , Antígeno B7-H1/metabolismo , Linfócitos do Interstício Tumoral/patologia , Carcinoma , Microambiente Tumoral , Neoplasias de Mama Triplo Negativas/patologia , Prognóstico , Biomarcadores Tumorais/metabolismo
2.
Chinese Journal of Pathology ; (12): 382-386, 2011.
Artigo em Chinês | WPRIM | ID: wpr-261772

RESUMO

<p><b>OBJECTIVE</b>To study the expression of prostate stem cell antigen (PSCA) at protein and mRNA levels in invasive micropapillary carcinoma of the breast (IMPC) and to analyze the relationship between PSCA expression and clinicopathologic features.</p><p><b>METHODS</b>The expression of PSCA protein was analyzed by immunohistochemistry (LSAB) in 66 cases of IMPC and 67 cases of invasive ductal carcinoma, not otherwise specified (IDC-NOS). The association between PSCA expression and clinicopathologic features was also analyzed in IMPC. Furthermore, RT-PCR was used to detect PSCA mRNA in 10 cases of primary IMPC and 10 cases of primary IDC-NOS with paired normal breast tissues, each from the same subject.</p><p><b>RESULTS</b>Immunohistochemical analysis revealed the overexpression of PSCA in 47 of 66 (71.2%) cases of IMPC and 35 of 67 (52.2%) IDC-NOS. Statistical analysis showed a significant difference of PSCA expression between IMPC and IDC-NOS (P = 0.024). In IMPC, the expression of PSCA was correlated with lymph nodes metastasis (P = 0.039). RT-PCR showed the mRNA level of PSCA was significantly higher in primary IMPC and IDC-NOS tissue than that in paired normal breast tissue (7/10 and 5/10, respectively), and it was also significantly higher in primary IMPC tissue than that in IDC-NOS tissue.</p><p><b>CONCLUSION</b>PSCA might play an important role in lymph node metastasis in IMPC.</p>


Assuntos
Feminino , Humanos , Antígenos de Neoplasias , Genética , Metabolismo , Neoplasias da Mama , Genética , Metabolismo , Patologia , Carcinoma Ductal de Mama , Genética , Metabolismo , Patologia , Carcinoma Papilar , Genética , Metabolismo , Patologia , Proteínas Ligadas por GPI , Genética , Metabolismo , Metástase Linfática , Invasividade Neoplásica , Proteínas de Neoplasias , Genética , Metabolismo , Estadiamento de Neoplasias , RNA Mensageiro , Metabolismo
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