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pmid:39090342

Association of GATA3 expression in triple-positive breast cancer with overall survival and immune cell infiltration.

Xiuwen Chen · Weilin Zhao · Yugang Huang · Senyuan Luo · Xianbin Tang · Qiong Yi

Scientific reports · 2024 doi:10.1038/s41598-024-68788-8

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Experiment

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Data

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pmid:39090342
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title
Association of GATA3 expression in triple-positive breast cancer with overall survival and immune cell infiltration.
doi
10.1038/s41598-024-68788-8
pmid
39090342
authors array · 6 items
[0]
Xiuwen Chen
[1]
Weilin Zhao
[2]
Yugang Huang
[3]
Senyuan Luo
[4]
Xianbin Tang
[5]
Qiong Yi
journal
Scientific reports
year
2024
abstract
Breast cancer remains a leading cause of cancer-related mortality among women, with triple-positive breast cancer (TPBC) being a particularly aggressive subtype. GATA binding protein 3 (GATA3) plays a crucial role in the luminal differentiation of breast epithelium and T-cell differentiation. However, the relationship between GATA3 and immune infiltration in TPBC remains unclear. This study collected and analyzed TPBC data from The Cancer Genome Atlas (TCGA), METABRIC, and GSE123845 databases. Univariate and multivariate Cox regression analyses, along with Kaplan-Meier survival analyses, were employed to assess the prognostic value of GATA3 and other clinical features. Subsequently, Gene Set Enrichment Analysis (GSEA) was conducted to explore the potential biological functions and regulatory mechanisms of GATA3 in TPBC. Additionally, ssGSEA analysis revealed the connection between GATA3 and immune infiltration. And the effects of neoadjuvant chemotherapy and immunotherapy on GATA3 expression were also explored. Finally, clinical samples were used to detect the relationship between GATA3 expression and tumor infiltrating lymphocyte (TIL) levels. Our results demonstrated that GATA3 was significantly overexpressed in TPBC tissues compared to normal tissues (P < 0.05). A positive correlation between GATA3 mRNA and protein levels was observed (R = 0.55, P < 0.05). Notably, high GATA3 expression was associated with poor overall survival (HR = 1.24, 95% confidence interval (CI) 1.25-11.76, P < 0.05). GSEA indicated significant enrichment of immune-related gene sets in low GATA3 expression groups. Furthermore, pathologic complete response (pCR) patients exhibited significantly lower GATA3 expression compared to residual disease (RD) patients. Mutation analysis revealed higher PIK3CA and TP53 mutation rates in high GATA3 expression groups. Finally, clinical validation data showed that the degree of TILs was significantly higher in the low GATA3 expression group. In conclusion, this study suggests that high GATA3 expression may be associated with poor prognosis and may reduce immune infiltration in TPBC.
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The single-sample Gene Set Enrichment Analysis (ssGSEA) method, implemented in the GSVA R package20, was used to estimate the ratio of immune cell infiltration between the GATA3 high- and low-expression subgroups.
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sections[6] "Association between GATA3 expression and immune infiltration" paragraph 2
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The single-sample Gene Set Enrichment Analysis (ssGSEA) method, implemented in the GSVA R package20, was used to estimate the ratio of immune cell infiltration between the GATA3 high- and low-expression subgroups.
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The TCGA dataset was obtained from https://portal.gdc.cancer.gov/. The METABRIC dataset was obtained from the https://www.cbioportal.org/study/summary?id=brca_metabric. The GSE123845 dataset was obtained from the https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc = GSE123845. Further inquiries can be directed to the corresponding author.
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The TCGA dataset was obtained from https://portal.gdc.cancer.gov/. The METABRIC dataset was obtained from the https://www.cbioportal.org/study/summary?id=brca_metabric. The GSE123845 dataset was obtained from the https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc = GSE123845. Further inquiries can be directed to the corresponding author.
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In conclusion, this study suggests that high GATA3 expression may be associated with poor prognosis and may reduce immune infiltration in TPBC.
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Multi-omics and immune profiling of breast cancers undergoing neoadjuvant chemotherapy identified dynamic cellular and molecular changes associated with clinical response
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capability_table_fingerprint
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lineage object · 4 fields
parent_id
pmid:39090342
parent_hash
sha256:e62ff6787395baeae4ff1717e8a5faa253918e06ac947d35b6edb5e03452670e
fork_of
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gaps array · 7 items
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asset:data:geo:GSE123845 licence not read
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method.reader_named_unmapped
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review.human_critique
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review.independent_reader
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review.machine_critique
assays array · 2 items
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role
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definition_version
99e1195c7d6f
required_operations array · 0 items
support_state
partial
source_hashes object · 1 field
assay_lexicon
99e1195c7d6f
confidence
0.99
evidence array · 4 items
[0]
3 protein expression and TILs, we first used immunohistochemical staining and H-score analysis to assess GATA
[1]
ion levels. Some example images of the GATA3 IHC results were shown in Figure S4. Based on st
[2]
al sample. High GATA3 protein expression (A, IHC × 100) but low TILs (B, HE × 100) in the hig
[3]
p. There is low GATA3 protein expression (C, IHC × 100) but high TILs (D, HE × 100) in the lo
order_basis
paper_text_order:5073
id
assay:1
[1] object · 11 fields
role
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f2132e96ae6c7a4e
required_operations array · 1 item
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survival_km
support_state
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source_hashes object · 1 field
dsl_catalogue
f2132e96ae6c7a4e
evidence array · 1 item
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Kaplan-Meier
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id
assay:2
Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:39090342", "kind": "science-record", "revision": 3, "content_hash": "sha256:fe1fd22c23c813edbcff7e339ae19c62e71aaf3afc402f3e0f11bf53cab20d15", "created_at": "2026-11-01T20:29:10Z", "updated_at": "2026-11-01T22:12:21Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Association of GATA3 expression in triple-positive breast cancer with overall survival and immune cell infiltration.", "doi": "10.1038/s41598-024-68788-8", "pmid": "39090342", "authors": ["Xiuwen Chen", "Weilin Zhao", "Yugang Huang", "Senyuan Luo", "Xianbin Tang", "Qiong Yi"], "journal": "Scientific reports", "year": 2024, "abstract": "Breast cancer remains a leading cause of cancer-related mortality among women, with triple-positive breast cancer (TPBC) being a particularly aggressive subtype. GATA binding protein 3 (GATA3) plays a crucial role in the luminal differentiation of breast epithelium and T-cell differentiation. However, the relationship between GATA3 and immune infiltration in TPBC remains unclear. This study collected and analyzed TPBC data from The Cancer Genome Atlas (TCGA), METABRIC, and GSE123845 databases. Univariate and multivariate Cox regression analyses, along with Kaplan-Meier survival analyses, were employed to assess the prognostic value of GATA3 and other clinical features. Subsequently, Gene Set Enrichment Analysis (GSEA) was conducted to explore the potential biological functions and regulatory mechanisms of GATA3 in TPBC. Additionally, ssGSEA analysis revealed the connection between GATA3 and immune infiltration. And the effects of neoadjuvant chemotherapy and immunotherapy on GATA3 expression were also explored. Finally, clinical samples were used to detect the relationship between GATA3 expression and tumor infiltrating lymphocyte (TIL) levels. Our results demonstrated that GATA3 was significantly overexpressed in TPBC tissues compared to normal tissues (P < 0.05). A positive correlation between GATA3 mRNA and protein levels was observed (R = 0.55, P < 0.05). Notably, high GATA3 expression was associated with poor overall survival (HR = 1.24, 95% confidence interval (CI) 1.25-11.76, P < 0.05). GSEA indicated significant enrichment of immune-related gene sets in low GATA3 expression groups. Furthermore, pathologic complete response (pCR) patients exhibited significantly lower GATA3 expression compared to residual disease (RD) patients. Mutation analysis revealed higher PIK3CA and TP53 mutation rates in high GATA3 expression groups. Finally, clinical validation data showed that the degree of TILs was significantly higher in the low GATA3 expression group. 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