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BIOMARKER:

ER overexpression

i
Other names: ESR1, Era, ESR, NR3A1, ER, ER beta
Entrez ID:
1year
Progesterone Receptor Expression Significantly Correlates with Recurrence Score Regardless of Menopausal Status in HR+/HER2- BC Patients (SABCS 2024)
In our cohort of HR+/HER2- early BC patients, patient menopausal status influenced the correlation between the RS and classical histopathological features. The rate of PgR expression was the only variable consistently correlating with the RS, regardless of menopausal status. Hence, the prognostic and predictive role of this, often overlooked, parameter deserves further investigation in larger and multicentric cohorts, along with a prospective validation.
Clinical
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HER-2 (Human epidermal growth factor receptor 2) • ER (Estrogen receptor) • PGR (Progesterone receptor)
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HER-2 negative • ER overexpression
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Oncotype DX Breast Recurrence Score®Test
1year
First-line (1L) ribociclib (RIB) + endocrine therapy (ET) vs combination chemotherapy (combo CT) in clinically aggressive HR+/HER2- advanced breast cancer (ABC): a subgroup analysis of RIGHT Choice by intrinsic subtype & gene & signature expression. (SABCS 2024)
Methods Pre/perimenopausal pts with no prior systemic therapy for aggressive HR+/HER2− ABC were randomized 1:1 to RIB + letrozole/anastrozole + goserelin or physician's choice of combo CT. Contrary results in the CT arm suggest that these signatures warrant further studies on their potential predictive value. These data are hypothesis generating and should be interpreted with caution due to small sample sizes.
Clinical • Metastases
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HER-2 (Human epidermal growth factor receptor 2) • ER (Estrogen receptor)
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HER-2 negative • ER expression • ER overexpression • ER-L
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nCounter® Breast Cancer 360™ Panel • nCounter® PanCancer IO 360™ Panel
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Kisqali (ribociclib) • letrozole • anastrozole • goserelin acetate
1year
Genetic Predisposition to Cancer Associated with a Germline Pathogenic BRCA2 Variant: A Clinical Case Report (SABCS 2024)
Subsequently, he received androgen deprivation therapy (ADT) for 6 months with triptorelin and bicalutamide...The pathological stage was pT1c pN1mi.The Oncotype DX study had a Recurrence Score (RS) of 22 points, leading to a recommendation for adjuvant chemotherapy with Docetaxel-Cyclophosphamide for 4 cycles, followed by tamoxifen...Early detection through screening and appropriate medical follow-up improves the prognosis in patients carrying PV in BRCA2. Therefore, risk control monitoring and adequate genetic counseling are necessary.
Clinical • Case report • BRCA Biomarker
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HER-2 (Human epidermal growth factor receptor 2) • ER (Estrogen receptor) • PGR (Progesterone receptor) • BRCA1 (Breast cancer 1, early onset) • BRCA2 (Breast cancer 2, early onset)
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HER-2 negative • ER expression • ER overexpression • HER-2 negative + AR positive + ER positive • HER-2 negative + ER positive • HER-2 negative + PGR positive
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Oncotype DX Breast Recurrence Score®Test
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docetaxel • tamoxifen • cyclophosphamide • bicalutamide • triptorelin
1year
Estrogen Regulated Genes Compel Apoptosis in Breast Cancer Cells, Whilst Stimulate Antitumor Activity in Peritumoral Immune Cells in a Janus-Faced Manner. (PubMed, Curr Oncol)
In breast cancers, there is no resistance to genotoxic or immune blocker therapies, but rather, the nonresponsive tumor cells exhaust all compensatory possibilities against therapeutic damages. Understanding the behavior and ambition of breast cancer cells may achieve a turn in therapy via applying supportive care instead of genotoxic measures.
Review • Journal • BRCA Biomarker • Immune cell
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HER-2 (Human epidermal growth factor receptor 2) • ER (Estrogen receptor) • BRCA1 (Breast cancer 1, early onset) • BRCA2 (Breast cancer 2, early onset)
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BRCA2 mutation • ER positive • BRCA1 mutation • HER-2 overexpression • ER negative • ER overexpression
over1year
Adavosertib-encapsulated metal-organic frameworks for p53-mutated gallbladder cancer treatment via synthetic lethality. (PubMed, Sci Bull (Beijing))
The conditional factor induced by ADA@MOF-EPL further enhances the antitumor efficacy while significantly reducing systemic toxicity. Moreover, ADA@MOF-EPL demonstrates similar antitumor abilities in other p53-mutated solid tumors, revealing its potential as a broad-spectrum antitumor drug.
Journal • Synthetic lethality
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ER (Estrogen receptor) • TP53 (Tumor protein P53)
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TP53 mutation • ER expression • ER overexpression
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adavosertib (AZD1775)
almost2years
Gastrin-releasing peptide receptor as a theranostic target in breast cancer: a systematic scoping review. (PubMed, Semin Nucl Med)
Clinical assessments suggested diagnostic value for GRPR-targeted theranostics in breast cancer patients, particularly those with high estrogen receptor expression. Nevertheless, in the therapeutic clinical context, paying attention to the radiation dose administered to the pancreas and kidneys is crucial.
Review • Journal
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ER (Estrogen receptor)
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ER expression • ER overexpression
2years
Patient Characteristics Associated with Growth of Patient-Derived Tumor Implants in Mice (Patient-Derived Xenografts). (PubMed, Cancers (Basel))
The use of steroids and/or antibiotics in the patient prior to sampling can also impact the likelihood of success in PDX development. Lastly, establishing a cutoff point for tumor growth rates could guide the decision-making process during PDX development.
Preclinical • Journal
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ER (Estrogen receptor)
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ER positive • MSI-H/dMMR • ER negative • ER overexpression
2years
Prognostic Role of HER2 Expression in Patients with ER-positive/HER2-negative Breast Cancer. Results from a Population-Based Cancer Registry Study (SABCS 2023)
The putative worse prognostic impact of HER2 expression in pts with ER-positive/HER2-negative BCs was not confirmed. The better outcome observed in pts with HER2 2+/FISH- BCs may be related to the known FISH-negative (HER2-non-amplified) status of this subgroup. These findings may help identify optimal patient inclusion criteria for clinical trials with novel anti-HER2 therapies in ER-positive/HER2-negative disease.
Clinical
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HER-2 (Human epidermal growth factor receptor 2) • ER (Estrogen receptor)
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HER-2 positive • ER positive • HER-2 negative • HER-2 expression • ER overexpression • ER positive + HER-2 negative
2years
Deciphering pregnancy-associated breast cancer: distinctive molecular profile and clinical implications from GEICAM/2017-07 EMBARCAM study (SABCS 2023)
Our study shows that PABC is potentially a clinical and molecular different entity with predominance of the basal-like subtype. Moreover, our results suggest the activation of oncogenic pathways related to cell proliferation, DNA damage repair and p53 mutations which may lead to a clinically more aggressive phenotype for PABC patients. Likewise, the enrichment of BRCAness and HRD signatures found in PABC patients in our study may suggest an increased genetic instability due to a breakdown in the DNA damage repair.
Clinical • PARP Biomarker • BRCA Biomarker
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HER-2 (Human epidermal growth factor receptor 2) • ER (Estrogen receptor) • PTEN (Phosphatase and tensin homolog) • HRD (Homologous Recombination Deficiency) • CD276 (CD276 Molecule) • CDK4 (Cyclin-dependent kinase 4) • CCNA2 (Cyclin A2) • TGFB1 (Transforming Growth Factor Beta 1) • CDC20 (Cell Division Cycle 20) • FAM83D (Family With Sequence Similarity 83 Member D) • TRIP13 (Thyroid Hormone Receptor Interactor 13) • CDK3 (Cyclin Dependent Kinase 3) • KIF2C (Kinesin Family Member 2C) • MAD2L1 (Mitotic Arrest Deficient 2 Like 1) • UBE2C (Ubiquitin Conjugating Enzyme E2 C)
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HER-2 positive • TP53 mutation • HR positive • HER-2 negative • HER-2 expression • HRD • CD276 expression • HR positive + HER-2 negative • ER expression • ER overexpression • HRD signature • PTEN mutation + HR positive
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Prosigna™ Breast Cancer Prognostic Gene Signature Assay • nCounter® Breast Cancer 360™ Panel
2years
NOTCH1-mutated chronic lymphocytic leukemia displays high endoplasmic reticulum stress response with druggable potential. (PubMed, Front Oncol)
Curcumin potentiated the apoptotic effect of venetoclax in NT1-M CLL cells...These cellular effects were associated with reduced NOTCH1 activity in leukemic cells and resulted in prolonged survival of curcumin-treated mice. Overall, our results indicate that ER stress induction in NT1-M CLL might represent a new therapeutic opportunity for these high-risk CLL patients and improve the therapeutic effect of drugs currently used in CLL.
Journal
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ER (Estrogen receptor) • NOTCH1 (Notch 1) • CD5 (CD5 Molecule) • ANXA5 (Annexin A5) • CASP4 (Caspase 4)
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NOTCH1 mutation • ER overexpression • NOTCH1 expression
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Venclexta (venetoclax)
2years
Optimization of small molecule degraders and antagonists for targeting estrogen receptor based on breast cancer: current status and future. (PubMed, Front Pharmacol)
Several drugs have been designed to specifically target ER in ER-positive (ER+) breast cancer, including selective estrogen receptor modulators (SERM) such as Tamoxifen...This paper provides a comprehensive review of the structural functions of ER and highlights recent advancements in SERD and SERCA-related small molecule drugs, especially focusing on their structural optimization strategies and future optimization directions. Additionally, the therapeutic potential and challenges of novel SERDs and SERCAs in breast cancer and other ER-related diseases have been discussed.
Review • Journal
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ER (Estrogen receptor)
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ER positive • ER overexpression
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tamoxifen
2years
EVOLVE-106, a T cell engager with integrated CD2 costimulation targeting B7-H4, is a precision therapy for estrogen and Her2 receptor low breast cancers (SITC 2023)
We found that HR+ breast cancer cell lines treated with the selective estrogen-degrader fulvestrant, displayed increased B7-H4 levels and combination treatment of EVOLVE-106 with fulvestrant increases EC50 of tumor killing by 5–8 fold. Conclusions These data support the potential positioning of EVOLVE-106 as a first-in-category immunotherapeutic approach for patients with Her2 receptor low breast cancers, and both estrogen receptor positive and negative tumors, including TNBC.
IO biomarker
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HER-2 (Human epidermal growth factor receptor 2) • ER (Estrogen receptor) • VTCN1 (V-Set Domain Containing T Cell Activation Inhibitor 1) • CD2 (CD2 Molecule)
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ER positive • HER-2 expression • VTCN1 underexpression • ER expression • ER overexpression
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fulvestrant