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Genetics, Treatment, and New Technologies of Hormone Receptor-Positive Breast Cancer
SIMPLE SUMMARY: In this review paper, we focused on the discussion of various important aspects of hormone receptor (HR)-positive breast cancer, including HR structure and signaling, genetics (epigenetics and gene mutations), gene expression-based assays, traditional and new drugs for treatment, and...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9954687/ https://www.ncbi.nlm.nih.gov/pubmed/36831644 http://dx.doi.org/10.3390/cancers15041303 |
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author | Sebastian, William Forchette, Lauren Donoughe, Kelsey Lun, Yibei Verma, Anisha Liu, Tuoen |
author_facet | Sebastian, William Forchette, Lauren Donoughe, Kelsey Lun, Yibei Verma, Anisha Liu, Tuoen |
author_sort | Sebastian, William |
collection | PubMed |
description | SIMPLE SUMMARY: In this review paper, we focused on the discussion of various important aspects of hormone receptor (HR)-positive breast cancer, including HR structure and signaling, genetics (epigenetics and gene mutations), gene expression-based assays, traditional and new drugs for treatment, and new technological uses in diagnosis and treatment. Particularly, we summarized the commonly mutated genes and abnormally methylated genes in HR-positive breast cancer and compared the common gene expression-based assays that are used in breast cancer as prognostic and/or predictive tools in detail. All of these topic discussions have not been fully described and summarized within other research or review articles. ABSTRACT: The current molecular classification divides breast cancer into four major subtypes, including luminal A, luminal B, HER2-positive, and basal-like, based on receptor gene expression profiling. Luminal A and luminal B are hormone receptor (HR, estrogen, and/or progesterone receptor)-positive and are the most common subtypes, accounting for around 50–60% and 15–20% of the total breast cancer cases, respectively. The drug treatment for HR-positive breast cancer includes endocrine therapy, HER2-targeted therapy (depending on the HER2 status), and chemotherapy (depending on the risk of recurrence). In this review, in addition to classification, we focused on discussing the important aspects of HR-positive breast cancer, including HR structure and signaling, genetics, including epigenetics and gene mutations, gene expression-based assays, the traditional and new drugs for treatment, and novel or new uses of technology in diagnosis and treatment. Particularly, we have summarized the commonly mutated genes and abnormally methylated genes in HR-positive breast cancer and compared four common gene expression-based assays that are used in breast cancer as prognostic and/or predictive tools in detail, including their clinical use, the factors being evaluated, patient demographics, and the scoring systems. All these topic discussions have not been fully described and summarized within other research or review articles. |
format | Online Article Text |
id | pubmed-9954687 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-99546872023-02-25 Genetics, Treatment, and New Technologies of Hormone Receptor-Positive Breast Cancer Sebastian, William Forchette, Lauren Donoughe, Kelsey Lun, Yibei Verma, Anisha Liu, Tuoen Cancers (Basel) Review SIMPLE SUMMARY: In this review paper, we focused on the discussion of various important aspects of hormone receptor (HR)-positive breast cancer, including HR structure and signaling, genetics (epigenetics and gene mutations), gene expression-based assays, traditional and new drugs for treatment, and new technological uses in diagnosis and treatment. Particularly, we summarized the commonly mutated genes and abnormally methylated genes in HR-positive breast cancer and compared the common gene expression-based assays that are used in breast cancer as prognostic and/or predictive tools in detail. All of these topic discussions have not been fully described and summarized within other research or review articles. ABSTRACT: The current molecular classification divides breast cancer into four major subtypes, including luminal A, luminal B, HER2-positive, and basal-like, based on receptor gene expression profiling. Luminal A and luminal B are hormone receptor (HR, estrogen, and/or progesterone receptor)-positive and are the most common subtypes, accounting for around 50–60% and 15–20% of the total breast cancer cases, respectively. The drug treatment for HR-positive breast cancer includes endocrine therapy, HER2-targeted therapy (depending on the HER2 status), and chemotherapy (depending on the risk of recurrence). In this review, in addition to classification, we focused on discussing the important aspects of HR-positive breast cancer, including HR structure and signaling, genetics, including epigenetics and gene mutations, gene expression-based assays, the traditional and new drugs for treatment, and novel or new uses of technology in diagnosis and treatment. Particularly, we have summarized the commonly mutated genes and abnormally methylated genes in HR-positive breast cancer and compared four common gene expression-based assays that are used in breast cancer as prognostic and/or predictive tools in detail, including their clinical use, the factors being evaluated, patient demographics, and the scoring systems. All these topic discussions have not been fully described and summarized within other research or review articles. MDPI 2023-02-18 /pmc/articles/PMC9954687/ /pubmed/36831644 http://dx.doi.org/10.3390/cancers15041303 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Sebastian, William Forchette, Lauren Donoughe, Kelsey Lun, Yibei Verma, Anisha Liu, Tuoen Genetics, Treatment, and New Technologies of Hormone Receptor-Positive Breast Cancer |
title | Genetics, Treatment, and New Technologies of Hormone Receptor-Positive Breast Cancer |
title_full | Genetics, Treatment, and New Technologies of Hormone Receptor-Positive Breast Cancer |
title_fullStr | Genetics, Treatment, and New Technologies of Hormone Receptor-Positive Breast Cancer |
title_full_unstemmed | Genetics, Treatment, and New Technologies of Hormone Receptor-Positive Breast Cancer |
title_short | Genetics, Treatment, and New Technologies of Hormone Receptor-Positive Breast Cancer |
title_sort | genetics, treatment, and new technologies of hormone receptor-positive breast cancer |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9954687/ https://www.ncbi.nlm.nih.gov/pubmed/36831644 http://dx.doi.org/10.3390/cancers15041303 |
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