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Nuclei-Guided Network for Breast Cancer Grading in HE-Stained Pathological Images †
Breast cancer grading methods based on hematoxylin-eosin (HE) stained pathological images can be summarized into two categories. The first category is to directly extract the pathological image features for breast cancer grading. However, unlike the coarse-grained problem of breast cancer classifica...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9185232/ https://www.ncbi.nlm.nih.gov/pubmed/35684680 http://dx.doi.org/10.3390/s22114061 |
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author | Yan, Rui Ren, Fei Li, Jintao Rao, Xiaosong Lv, Zhilong Zheng, Chunhou Zhang, Fa |
author_facet | Yan, Rui Ren, Fei Li, Jintao Rao, Xiaosong Lv, Zhilong Zheng, Chunhou Zhang, Fa |
author_sort | Yan, Rui |
collection | PubMed |
description | Breast cancer grading methods based on hematoxylin-eosin (HE) stained pathological images can be summarized into two categories. The first category is to directly extract the pathological image features for breast cancer grading. However, unlike the coarse-grained problem of breast cancer classification, breast cancer grading is a fine-grained classification problem, so general methods cannot achieve satisfactory results. The second category is to apply the three evaluation criteria of the Nottingham Grading System (NGS) separately, and then integrate the results of the three criteria to obtain the final grading result. However, NGS is only a semiquantitative evaluation method, and there may be far more image features related to breast cancer grading. In this paper, we proposed a Nuclei-Guided Network (NGNet) for breast invasive ductal carcinoma (IDC) grading in pathological images. The proposed nuclei-guided attention module plays the role of nucleus attention, so as to learn more nuclei-related feature representations for breast IDC grading. In addition, the proposed nuclei-guided fusion module in the fusion process of different branches can further enable the network to focus on learning nuclei-related features. Overall, under the guidance of nuclei-related features, the entire NGNet can learn more fine-grained features for breast IDC grading. The experimental results show that the performance of the proposed method is better than that of state-of-the-art method. In addition, we released a well-labeled dataset with 3644 pathological images for breast IDC grading. This dataset is currently the largest publicly available breast IDC grading dataset and can serve as a benchmark to facilitate a broader study of breast IDC grading. |
format | Online Article Text |
id | pubmed-9185232 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-91852322022-06-11 Nuclei-Guided Network for Breast Cancer Grading in HE-Stained Pathological Images † Yan, Rui Ren, Fei Li, Jintao Rao, Xiaosong Lv, Zhilong Zheng, Chunhou Zhang, Fa Sensors (Basel) Article Breast cancer grading methods based on hematoxylin-eosin (HE) stained pathological images can be summarized into two categories. The first category is to directly extract the pathological image features for breast cancer grading. However, unlike the coarse-grained problem of breast cancer classification, breast cancer grading is a fine-grained classification problem, so general methods cannot achieve satisfactory results. The second category is to apply the three evaluation criteria of the Nottingham Grading System (NGS) separately, and then integrate the results of the three criteria to obtain the final grading result. However, NGS is only a semiquantitative evaluation method, and there may be far more image features related to breast cancer grading. In this paper, we proposed a Nuclei-Guided Network (NGNet) for breast invasive ductal carcinoma (IDC) grading in pathological images. The proposed nuclei-guided attention module plays the role of nucleus attention, so as to learn more nuclei-related feature representations for breast IDC grading. In addition, the proposed nuclei-guided fusion module in the fusion process of different branches can further enable the network to focus on learning nuclei-related features. Overall, under the guidance of nuclei-related features, the entire NGNet can learn more fine-grained features for breast IDC grading. The experimental results show that the performance of the proposed method is better than that of state-of-the-art method. In addition, we released a well-labeled dataset with 3644 pathological images for breast IDC grading. This dataset is currently the largest publicly available breast IDC grading dataset and can serve as a benchmark to facilitate a broader study of breast IDC grading. MDPI 2022-05-27 /pmc/articles/PMC9185232/ /pubmed/35684680 http://dx.doi.org/10.3390/s22114061 Text en © 2022 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 | Article Yan, Rui Ren, Fei Li, Jintao Rao, Xiaosong Lv, Zhilong Zheng, Chunhou Zhang, Fa Nuclei-Guided Network for Breast Cancer Grading in HE-Stained Pathological Images † |
title | Nuclei-Guided Network for Breast Cancer Grading in HE-Stained Pathological Images † |
title_full | Nuclei-Guided Network for Breast Cancer Grading in HE-Stained Pathological Images † |
title_fullStr | Nuclei-Guided Network for Breast Cancer Grading in HE-Stained Pathological Images † |
title_full_unstemmed | Nuclei-Guided Network for Breast Cancer Grading in HE-Stained Pathological Images † |
title_short | Nuclei-Guided Network for Breast Cancer Grading in HE-Stained Pathological Images † |
title_sort | nuclei-guided network for breast cancer grading in he-stained pathological images † |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9185232/ https://www.ncbi.nlm.nih.gov/pubmed/35684680 http://dx.doi.org/10.3390/s22114061 |
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