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Kindlin-2 could influence breast nodule elasticity and improve lymph node metastasis in invasive breast cancer
This study investigated the relationship between quantitative parameters of shear wave elastography (SWE, maximum elasticity [Emax], minimum elasticity [Emin], mean elasticity [Emean]), collagen intensity and Kindlin-2 expression in benign and malignant breast nodules, and if Kindlin-2 expression is...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5533728/ https://www.ncbi.nlm.nih.gov/pubmed/28755003 http://dx.doi.org/10.1038/s41598-017-07075-1 |
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author | Xue, Xiaowei Li, Junlai Wan, Wenbo Shi, Xianquan Zheng, Yiqiong |
author_facet | Xue, Xiaowei Li, Junlai Wan, Wenbo Shi, Xianquan Zheng, Yiqiong |
author_sort | Xue, Xiaowei |
collection | PubMed |
description | This study investigated the relationship between quantitative parameters of shear wave elastography (SWE, maximum elasticity [Emax], minimum elasticity [Emin], mean elasticity [Emean]), collagen intensity and Kindlin-2 expression in benign and malignant breast nodules, and if Kindlin-2 expression is related with lymph node metastasis. A total of 102 breast nodules from 102 patients were included in our study who underwent ultrasound elastography before surgery or core needle biopsy. There was a significant difference between benign and malignant breast nodules in Emax, Emean, collagen intensity and Kindlin-2 expression, but it had no difference in Emin. Collagen intensity and Kindlin-2 expression both correlated positively with Emax, but not with Emean. Among 38 malignant breast nodules, the average Emax of the metastasis group was higher than that of the non-metastasis group, but it had no statistical significance. Compared with the non-metastasis group, Kindlin-2 expression was considerably higher in the metastasis group. However, there was no difference in collagen intensity between the metastasis group and the non-metastasis group. In conclusion, Kindlin-2 and collagen might contribute to breast nodule elasticity through molecular mechanisms. In breast cancer, overexpression of Kindlin-2 might be a risk factor for lymph node metastasis. |
format | Online Article Text |
id | pubmed-5533728 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55337282017-08-03 Kindlin-2 could influence breast nodule elasticity and improve lymph node metastasis in invasive breast cancer Xue, Xiaowei Li, Junlai Wan, Wenbo Shi, Xianquan Zheng, Yiqiong Sci Rep Article This study investigated the relationship between quantitative parameters of shear wave elastography (SWE, maximum elasticity [Emax], minimum elasticity [Emin], mean elasticity [Emean]), collagen intensity and Kindlin-2 expression in benign and malignant breast nodules, and if Kindlin-2 expression is related with lymph node metastasis. A total of 102 breast nodules from 102 patients were included in our study who underwent ultrasound elastography before surgery or core needle biopsy. There was a significant difference between benign and malignant breast nodules in Emax, Emean, collagen intensity and Kindlin-2 expression, but it had no difference in Emin. Collagen intensity and Kindlin-2 expression both correlated positively with Emax, but not with Emean. Among 38 malignant breast nodules, the average Emax of the metastasis group was higher than that of the non-metastasis group, but it had no statistical significance. Compared with the non-metastasis group, Kindlin-2 expression was considerably higher in the metastasis group. However, there was no difference in collagen intensity between the metastasis group and the non-metastasis group. In conclusion, Kindlin-2 and collagen might contribute to breast nodule elasticity through molecular mechanisms. In breast cancer, overexpression of Kindlin-2 might be a risk factor for lymph node metastasis. Nature Publishing Group UK 2017-07-28 /pmc/articles/PMC5533728/ /pubmed/28755003 http://dx.doi.org/10.1038/s41598-017-07075-1 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Xue, Xiaowei Li, Junlai Wan, Wenbo Shi, Xianquan Zheng, Yiqiong Kindlin-2 could influence breast nodule elasticity and improve lymph node metastasis in invasive breast cancer |
title | Kindlin-2 could influence breast nodule elasticity and improve lymph node metastasis in invasive breast cancer |
title_full | Kindlin-2 could influence breast nodule elasticity and improve lymph node metastasis in invasive breast cancer |
title_fullStr | Kindlin-2 could influence breast nodule elasticity and improve lymph node metastasis in invasive breast cancer |
title_full_unstemmed | Kindlin-2 could influence breast nodule elasticity and improve lymph node metastasis in invasive breast cancer |
title_short | Kindlin-2 could influence breast nodule elasticity and improve lymph node metastasis in invasive breast cancer |
title_sort | kindlin-2 could influence breast nodule elasticity and improve lymph node metastasis in invasive breast cancer |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5533728/ https://www.ncbi.nlm.nih.gov/pubmed/28755003 http://dx.doi.org/10.1038/s41598-017-07075-1 |
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