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Clinical and pathological features analysis of invasive breast cancer with microcalcification
PURPOSE: Microcalcification (MC) is a valuable diagnostic indicator to detect invasive breast cancer (IBC). This study aimed to determine the clinicopathological features of IBC with MC and detect biomarkers related to the potential mechanism of the MC formation in IBC. METHODS: Data from 364 patien...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10242326/ https://www.ncbi.nlm.nih.gov/pubmed/36971046 http://dx.doi.org/10.1002/cam4.5848 |
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author | Tian, Yao Zhao, Lu Gui, Zhengwei Liu, Shiyang Liu, Chenguang Yu, Tianyao Zhang, Lin |
author_facet | Tian, Yao Zhao, Lu Gui, Zhengwei Liu, Shiyang Liu, Chenguang Yu, Tianyao Zhang, Lin |
author_sort | Tian, Yao |
collection | PubMed |
description | PURPOSE: Microcalcification (MC) is a valuable diagnostic indicator to detect invasive breast cancer (IBC). This study aimed to determine the clinicopathological features of IBC with MC and detect biomarkers related to the potential mechanism of the MC formation in IBC. METHODS: Data from 364 patients with IBC were collected for the clinical characteristic analysis. The analysis of clinical data helped us to establish a predictive model of axillary node metastasis (ANM) before surgery. In addition, 49 tissue samples of IBC patients were collected to test the protein levels of osteocalcin (OCN) and hypoxia‐inducible factor‐1α (HIF‐1α) by immunohistochemistry. RESULTS: Significant differences were observed in tumor size, age, ANM, HER2(+), TNM stage, and mutant P53 between samples from IBC patients with MC and samples from IBC patients without MC. Younger age, a larger tumor size, a higher number of childbirths, and MC were independent predictors for ANM in IBC. HIF‐1α protein level was higher in tumor tissue than in normal tissue. High protein levels of OCN and HIF‐1α are related to the complication of MC in IBC. Of the patients that exhibited high HIF‐1α protein levels, the percentage of high OCN protein levels was larger in patients with ANM. CONCLUSION: Based on this study, we concluded that patients with MC had a comparatively poor prognosis. MC was an independent predictive factor associated with the risk of ANM. High protein levels of OCN and HIF‐1α were associated with MC and ANM, which were also related to poor prognosis. OCN and HIF‐1α had a positive correlation in IBC. |
format | Online Article Text |
id | pubmed-10242326 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-102423262023-06-07 Clinical and pathological features analysis of invasive breast cancer with microcalcification Tian, Yao Zhao, Lu Gui, Zhengwei Liu, Shiyang Liu, Chenguang Yu, Tianyao Zhang, Lin Cancer Med RESEARCH ARTICLES PURPOSE: Microcalcification (MC) is a valuable diagnostic indicator to detect invasive breast cancer (IBC). This study aimed to determine the clinicopathological features of IBC with MC and detect biomarkers related to the potential mechanism of the MC formation in IBC. METHODS: Data from 364 patients with IBC were collected for the clinical characteristic analysis. The analysis of clinical data helped us to establish a predictive model of axillary node metastasis (ANM) before surgery. In addition, 49 tissue samples of IBC patients were collected to test the protein levels of osteocalcin (OCN) and hypoxia‐inducible factor‐1α (HIF‐1α) by immunohistochemistry. RESULTS: Significant differences were observed in tumor size, age, ANM, HER2(+), TNM stage, and mutant P53 between samples from IBC patients with MC and samples from IBC patients without MC. Younger age, a larger tumor size, a higher number of childbirths, and MC were independent predictors for ANM in IBC. HIF‐1α protein level was higher in tumor tissue than in normal tissue. High protein levels of OCN and HIF‐1α are related to the complication of MC in IBC. Of the patients that exhibited high HIF‐1α protein levels, the percentage of high OCN protein levels was larger in patients with ANM. CONCLUSION: Based on this study, we concluded that patients with MC had a comparatively poor prognosis. MC was an independent predictive factor associated with the risk of ANM. High protein levels of OCN and HIF‐1α were associated with MC and ANM, which were also related to poor prognosis. OCN and HIF‐1α had a positive correlation in IBC. John Wiley and Sons Inc. 2023-03-27 /pmc/articles/PMC10242326/ /pubmed/36971046 http://dx.doi.org/10.1002/cam4.5848 Text en © 2023 The Authors. Cancer Medicine published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | RESEARCH ARTICLES Tian, Yao Zhao, Lu Gui, Zhengwei Liu, Shiyang Liu, Chenguang Yu, Tianyao Zhang, Lin Clinical and pathological features analysis of invasive breast cancer with microcalcification |
title | Clinical and pathological features analysis of invasive breast cancer with microcalcification |
title_full | Clinical and pathological features analysis of invasive breast cancer with microcalcification |
title_fullStr | Clinical and pathological features analysis of invasive breast cancer with microcalcification |
title_full_unstemmed | Clinical and pathological features analysis of invasive breast cancer with microcalcification |
title_short | Clinical and pathological features analysis of invasive breast cancer with microcalcification |
title_sort | clinical and pathological features analysis of invasive breast cancer with microcalcification |
topic | RESEARCH ARTICLES |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10242326/ https://www.ncbi.nlm.nih.gov/pubmed/36971046 http://dx.doi.org/10.1002/cam4.5848 |
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