Related Experiment Video
Updated: Feb 27, 2026

11:12
Optimization of a Multiplex RNA-based Expression Assay Using Breast Cancer Archival Material
Published on: August 1, 2018
8.5K
Estrogen Receptor-Low Positive (ER-Low) Breast Cancer: A Unique Clinical and Pathological Entity
Gavino Faa1,2, Eleonora Lai3, Pina Ziranu3
1Department of Medical Sciences and Public Health, University of Cagliari, AOU Cagliari, 09124 Cagliari, Italy.
Current Oncology (Toronto, Ont.)
|February 26, 2026
Summary
ER-low breast cancer, defined by 1-9% ER expression, shares traits with triple-negative breast cancer. AI tools show promise for accurate assessment and personalized treatment strategies.
Area of Science:
- Oncology
- Pathology
- Biomedical Engineering
Background:
- ER-low breast cancer (1-9% ER expression) is a distinct subtype.
- It exhibits molecular and clinical similarities to triple-negative breast cancer.
- Accurate ER assessment is challenging due to methodological variability.
Purpose of the Study:
- To review current insights into ER-low breast cancer.
- To discuss evolving therapeutic strategies.
- To explore the role of AI in managing this subtype.
Main Methods:
- Literature review of pathological and clinical data.
- Analysis of treatment responses, including chemotherapy and chemo-immunotherapy.
- Evaluation of emerging artificial intelligence tools for ER quantification.
Main Results:
- ER-low tumors demonstrate sensitivity to chemotherapy and chemo-immunotherapy.
- These tumors share aggressive behavior and molecular signatures with triple-negative breast cancer.
- AI tools, including digital pathology and deep learning, show potential for improved ER assessment and patient stratification.
Conclusions:
- ER-low breast cancer requires tailored management strategies.
- Chemotherapy and chemo-immunotherapy are promising treatment options.
- AI-driven approaches offer future potential for personalized treatment optimization.
Related Concept Videos
Transducer Mechanism: Nuclear Receptors
3.6K
Nuclear receptors, or NRs, are unique transcription factors that regulate gene transcription and affect the cellular pathways involved in reproduction, development, or metabolism. Their ability to be stimulated by small lipophilic ligands and control vital cellular processes makes them ideal drug targets. Nearly 10-15% of currently prescribed drugs target these receptors.
About 48 different soluble family members of nuclear receptors are identified that can be divided into two main classes:
About 48 different soluble family members of nuclear receptors are identified that can be divided into two main classes:
3.6K
lncRNA - Long Non-coding RNAs
10.0K
In humans, more than 80% of the genome gets transcribed. However, only around 2% of the genome codes for proteins. The remaining part produces non-coding RNAs which includes ribosomal RNAs, transfer RNAs, telomerase RNAs, and regulatory RNAs, among other types. A large number of regulatory non-coding RNAs have been classified into two groups depending upon their length – small non-coding RNAs, such as microRNA, which are less than 200 nucleotides in length, and long non-coding RNA...
10.0K

