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CXCR4 and breast cancer are reported together in 7 articles.
Gene
CXCR4
- HGNC
- HGNC:2561
39articles
39mentions
0variants with confirmed gene link
Most co-reported phenotypes (articles)
Phenotype
Breast cancer
1,211articles
1,211mentions
12co-reported genes shown
Most co-reported genes (articles)
Counts are literature co-mentions in SaudiVarKB, not clinical or causal assertions. Gene details: HGNC; variant status: ClinVar via dbSNP.
Publications
7 records shown · first 60Exploring the landscape of autoimmune disorder-associated genes and their impact on immune microenvironment in breast cancer patients.
PMID 40672619 | PMCID PMC12261193 | DOI 10.62347/EANH4082 · American journal of translational research · 2025 · 10 validated mentions
Evidence preview
| Type | Entity | Source evidence | Confidence | Extractor |
|---|---|---|---|---|
| gene | CXCR4 | “Ten hub genes were identified, with CXCR4, MMP9, CTLA4, CD80, and ICOS upregulated, and IL6, KIT, PPARG, SLC2A4, and CEBPA downregulated.” | 0.98 | hgnc_dict_v1 |
| phenotype | breast cancer | “Exploring the landscape of autoimmune disorder-associated genes and their impact on immune microenvironment in breast cancer patients.” | 0.98 | phenotype_alias_lexicon_v2 |
| gene | MMP9 | “Ten hub genes were identified, with CXCR4, MMP9, CTLA4, CD80, and ICOS upregulated, and IL6, KIT, PPARG, SLC2A4, and CEBPA downregulated.” | 0.98 | hgnc_dict_v1 |
| gene | CTLA4 | “Ten hub genes were identified, with CXCR4, MMP9, CTLA4, CD80, and ICOS upregulated, and IL6, KIT, PPARG, SLC2A4, and CEBPA downregulated.” | 0.98 | hgnc_dict_v1 |
Unravelling the therapeutic potential of dual TGFβ-1 and CXCR4 inhibition in breast cancer using computational strategies.
PMID 41348904 | PMCID PMC12680324 | DOI 10.1371/journal.pone.0323665 · PloS one · 2025 · 6 validated mentions
Evidence preview
| Type | Entity | Source evidence | Confidence | Extractor |
|---|---|---|---|---|
| gene | CXCR4 | “Unravelling the therapeutic potential of dual TGFβ-1 and CXCR4 inhibition in breast cancer using computational strategies.” | 0.98 | hgnc_dict_v1 |
| phenotype | breast cancer | “Unravelling the therapeutic potential of dual TGFβ-1 and CXCR4 inhibition in breast cancer using computational strategies.” | 0.98 | phenotype_alias_lexicon_v2 |
| gene | IL19 | “TGFβ-1, IL19, CXCR4, BMP1, VCAN, and WNT2 have been implicated to be instrumental to critical oncogenic pathways; however, their cumulative contribution toward the pathophysiology of BC has not yet been investigated.” | 0.98 | hgnc_dict_v1 |
| gene | BMP1 | “TGFβ-1, IL19, CXCR4, BMP1, VCAN, and WNT2 have been implicated to be instrumental to critical oncogenic pathways; however, their cumulative contribution toward the pathophysiology of BC has not yet been investigated.” | 0.98 | hgnc_dict_v1 |
CXCR4 expression is elevated in TNBC patient derived samples and Z-guggulsterone abrogates tumor progression by targeting CXCL12/CXCR4 signaling axis in preclinical breast cancer model.
PMID 37290620 | DOI 10.1016/j.envres.2023.116335 · Environmental research · 2023 · 3 validated mentions
Evidence preview
| Type | Entity | Source evidence | Confidence | Extractor |
|---|---|---|---|---|
| gene | CXCR4 | “CXCR4 expression is elevated in TNBC patient derived samples and Z-guggulsterone abrogates tumor progression by targeting CXCL12/CXCR4 signaling axis in preclinical breast cancer model.” | 0.98 | hgnc_dict_v1 |
| phenotype | breast cancer | “CXCR4 expression is elevated in TNBC patient derived samples and Z-guggulsterone abrogates tumor progression by targeting CXCL12/CXCR4 signaling axis in preclinical breast cancer model.” | 0.98 | phenotype_alias_lexicon_v2 |
| gene | CXCL12 | “CXCR4 expression is elevated in TNBC patient derived samples and Z-guggulsterone abrogates tumor progression by targeting CXCL12/CXCR4 signaling axis in preclinical breast cancer model.” | 0.98 | hgnc_dict_v1 |
Recurrence biomarkers of triple negative breast cancer treated with neoadjuvant chemotherapy and anti-EGFR antibodies.
PMID 34535679 | PMCID PMC8448841 | DOI 10.1038/s41523-021-00334-5 · NPJ breast cancer · 2021 · 3 validated mentions
Evidence preview
| Type | Entity | Source evidence | Confidence | Extractor |
|---|---|---|---|---|
| gene | CXCR4 | “In post-NAT residual tumors, RR cases showed high expression of SOX2 and CXCR4.” | 0.98 | hgnc_dict_v1 |
| phenotype | breast cancer | “Recurrence biomarkers of triple negative breast cancer treated with neoadjuvant chemotherapy and anti-EGFR antibodies.” | 0.98 | phenotype_alias_lexicon_v2 |
| gene | SOX2 | “In post-NAT residual tumors, RR cases showed high expression of SOX2 and CXCR4.” | 0.98 | hgnc_dict_v1 |
The prognostic value of JUNB-positive CTCs in metastatic breast cancer: from bioinformatics to phenotypic characterization.
PMID 31370904 | PMCID PMC6676640 | DOI 10.1186/s13058-019-1166-4 · Breast cancer research : BCR · 2019 · 7 validated mentions
Evidence preview
| Type | Entity | Source evidence | Confidence | Extractor |
|---|---|---|---|---|
| gene | CXCR4 | “Among these genes, the chemokine receptor CXCR4 plays a central role.” | 0.98 | hgnc_dict_v1 |
| phenotype | breast cancer | “The prognostic value of JUNB-positive CTCs in metastatic breast cancer: from bioinformatics to phenotypic characterization.” | 0.98 | phenotype_alias_lexicon_v2 |
| gene | JUNB | “After prioritization according to the CXCR4 corresponding pathways, five molecules (JUNB, YWHAB, TYROBP, NFYA, and PRDX1) were selected for further analysis in biological samples.” | 0.98 | hgnc_dict_v1 |
| gene | YWHAB | “After prioritization according to the CXCR4 corresponding pathways, five molecules (JUNB, YWHAB, TYROBP, NFYA, and PRDX1) were selected for further analysis in biological samples.” | 0.98 | hgnc_dict_v1 |
Thymoquinone Inhibits Bone Metastasis of Breast Cancer Cells Through Abrogation of the CXCR4 Signaling Axis.
PMID 30564115 | PMCID PMC6288203 | DOI 10.3389/fphar.2018.01294 · Frontiers in pharmacology · 2018 · 2 validated mentions
Evidence preview
| Type | Entity | Source evidence | Confidence | Extractor |
|---|---|---|---|---|
| gene | CXCR4 | “Thymoquinone Inhibits Bone Metastasis of Breast Cancer Cells Through Abrogation of the CXCR4 Signaling Axis.” | 0.98 | hgnc_dict_v1 |
| phenotype | breast cancer | “Thymoquinone Inhibits Bone Metastasis of Breast Cancer Cells Through Abrogation of the CXCR4 Signaling Axis.” | 0.98 | phenotype_alias_lexicon_v2 |
Posttranscriptional control of the chemokine receptor CXCR4 expression in cancer cells.
PMID 24692066 | PMCID PMC4146410 | DOI 10.1093/carcin/bgu080 · Carcinogenesis · 2014 · 5 validated mentions
Evidence preview
| Type | Entity | Source evidence | Confidence | Extractor |
|---|---|---|---|---|
| gene | CXCR4 | “Posttranscriptional control of the chemokine receptor CXCR4 expression in cancer cells.” | 0.98 | hgnc_dict_v1 |
| phenotype | breast cancer | “In the invasive breast cancer phenotype, aberrant expression of CXCR4 is linked to both TTP deficiency and HuR overexpression.” | 0.98 | phenotype_alias_lexicon_v2 |
| gene | ZFP36 | “Here, we find that CXCR4 harbors AU-rich elements (AREs) in the 3'-untranslated region (3'-UTR) that bind and respond to the RNA-binding proteins, tristetraprolin (TTP/ZFP36) and HuR (ELAVL1).” | 0.98 | hgnc_dict_v1 |
| gene | ELAVL1 | “Here, we find that CXCR4 harbors AU-rich elements (AREs) in the 3'-untranslated region (3'-UTR) that bind and respond to the RNA-binding proteins, tristetraprolin (TTP/ZFP36) and HuR (ELAVL1).” | 0.98 | hgnc_dict_v1 |