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Comprehensive Analysis of the Expression and Prognostic Value of SPINT1/2 in Breast Carcinoma
BACKGROUND: Hepatocyte growth factor (HGF) signaling plays a plethora of roles in tumorigenesis and progression in many cancer types. As HGF activator inhibitors, serine protease inhibitor, Kunitz types 1 and 2 (SPINT1 and SPINT2) have been reported to be differentially expressed in breast cancer, b...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8351597/ https://www.ncbi.nlm.nih.gov/pubmed/34381422 http://dx.doi.org/10.3389/fendo.2021.665666 |
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author | Wu, Qiulin Yin, Guobing Luo, Jing Zhang, Yingzi Ai, Tiantian Tian, Jiao Jin, Yudi Lei, Jinwei Liu, Shengchun |
author_facet | Wu, Qiulin Yin, Guobing Luo, Jing Zhang, Yingzi Ai, Tiantian Tian, Jiao Jin, Yudi Lei, Jinwei Liu, Shengchun |
author_sort | Wu, Qiulin |
collection | PubMed |
description | BACKGROUND: Hepatocyte growth factor (HGF) signaling plays a plethora of roles in tumorigenesis and progression in many cancer types. As HGF activator inhibitors, serine protease inhibitor, Kunitz types 1 and 2 (SPINT1 and SPINT2) have been reported to be differentially expressed in breast cancer, but their prognostic significance and functioning mechanism remain unclear. METHODS: In our study, multiple databases and bioinformatics tools were used to investigate SPINT1/2 expression profiles, prognostic significance, genetic alteration, methylation, and regulatory network in breast carcinoma. RESULTS: SPINT1/2 expression was upregulated in breast cancer, and was relatively higher in human epidermal growth factor receptor 2 (HER2) and node positive patients. Elevated SPINT1/2 expression was significantly correlated with a poorer prognosis. Genetic alterations and SPINT1/2 hypomethylation were observed. In breast carcinoma, SPINT1/2 were reciprocally correlated and shared common co-expressed genes. Gene ontology (GO) and the Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment analysis showed that their common co-expressed genes were primarily involved in regulating cell attachment and migration. CONCLUSIONS: Our study identified the expression profiles, prognostic significance and potential roles of SPINT1/2 in breast carcinoma. These study results showed that the SPINT1/2 were potential prognostic biomarker for patients with breast cancer. |
format | Online Article Text |
id | pubmed-8351597 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-83515972021-08-10 Comprehensive Analysis of the Expression and Prognostic Value of SPINT1/2 in Breast Carcinoma Wu, Qiulin Yin, Guobing Luo, Jing Zhang, Yingzi Ai, Tiantian Tian, Jiao Jin, Yudi Lei, Jinwei Liu, Shengchun Front Endocrinol (Lausanne) Endocrinology BACKGROUND: Hepatocyte growth factor (HGF) signaling plays a plethora of roles in tumorigenesis and progression in many cancer types. As HGF activator inhibitors, serine protease inhibitor, Kunitz types 1 and 2 (SPINT1 and SPINT2) have been reported to be differentially expressed in breast cancer, but their prognostic significance and functioning mechanism remain unclear. METHODS: In our study, multiple databases and bioinformatics tools were used to investigate SPINT1/2 expression profiles, prognostic significance, genetic alteration, methylation, and regulatory network in breast carcinoma. RESULTS: SPINT1/2 expression was upregulated in breast cancer, and was relatively higher in human epidermal growth factor receptor 2 (HER2) and node positive patients. Elevated SPINT1/2 expression was significantly correlated with a poorer prognosis. Genetic alterations and SPINT1/2 hypomethylation were observed. In breast carcinoma, SPINT1/2 were reciprocally correlated and shared common co-expressed genes. Gene ontology (GO) and the Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment analysis showed that their common co-expressed genes were primarily involved in regulating cell attachment and migration. CONCLUSIONS: Our study identified the expression profiles, prognostic significance and potential roles of SPINT1/2 in breast carcinoma. These study results showed that the SPINT1/2 were potential prognostic biomarker for patients with breast cancer. Frontiers Media S.A. 2021-07-26 /pmc/articles/PMC8351597/ /pubmed/34381422 http://dx.doi.org/10.3389/fendo.2021.665666 Text en Copyright © 2021 Wu, Yin, Luo, Zhang, Ai, Tian, Jin, Lei and Liu https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Endocrinology Wu, Qiulin Yin, Guobing Luo, Jing Zhang, Yingzi Ai, Tiantian Tian, Jiao Jin, Yudi Lei, Jinwei Liu, Shengchun Comprehensive Analysis of the Expression and Prognostic Value of SPINT1/2 in Breast Carcinoma |
title | Comprehensive Analysis of the Expression and Prognostic Value of SPINT1/2 in Breast Carcinoma |
title_full | Comprehensive Analysis of the Expression and Prognostic Value of SPINT1/2 in Breast Carcinoma |
title_fullStr | Comprehensive Analysis of the Expression and Prognostic Value of SPINT1/2 in Breast Carcinoma |
title_full_unstemmed | Comprehensive Analysis of the Expression and Prognostic Value of SPINT1/2 in Breast Carcinoma |
title_short | Comprehensive Analysis of the Expression and Prognostic Value of SPINT1/2 in Breast Carcinoma |
title_sort | comprehensive analysis of the expression and prognostic value of spint1/2 in breast carcinoma |
topic | Endocrinology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8351597/ https://www.ncbi.nlm.nih.gov/pubmed/34381422 http://dx.doi.org/10.3389/fendo.2021.665666 |
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