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Overexpression of SKA3 correlates with poor prognosis in female early breast cancer

BACKGROUND: Spindle and kinetochore associated complex subunit 3 (SKA3) plays an important role in tumorigenesis and the progression of various tumors. But the relationship between SKA3 and early breast cancer remains unclear. The study aimed to explore the prognostic significance of SKA3 in breast...

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Autores principales: Zhong, Yue, Zhuang, Zhenjie, Mo, Peiju, Lin, Mandi, Gong, Jiaqian, Huang, Jiarong, Mo, Haiyan, Lu, Yuyun, Huang, Mei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PeerJ Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8675262/
https://www.ncbi.nlm.nih.gov/pubmed/34993016
http://dx.doi.org/10.7717/peerj.12506
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author Zhong, Yue
Zhuang, Zhenjie
Mo, Peiju
Lin, Mandi
Gong, Jiaqian
Huang, Jiarong
Mo, Haiyan
Lu, Yuyun
Huang, Mei
author_facet Zhong, Yue
Zhuang, Zhenjie
Mo, Peiju
Lin, Mandi
Gong, Jiaqian
Huang, Jiarong
Mo, Haiyan
Lu, Yuyun
Huang, Mei
author_sort Zhong, Yue
collection PubMed
description BACKGROUND: Spindle and kinetochore associated complex subunit 3 (SKA3) plays an important role in tumorigenesis and the progression of various tumors. But the relationship between SKA3 and early breast cancer remains unclear. The study aimed to explore the prognostic significance of SKA3 in breast cancer. METHODS: In the study, SKA3 expression was initially assessed using the Oncomine database and The Cancer Genome Atlas database (TCGA). Then, we presented validation results for RT-qPCR (quantitative reverse transcription PCR) and ELISA (enzyme-linked immunosorbent assay). The relationship between clinical characteristics and SKA3 expression was assessed by Chi-square test and Fisher’s exact test. Kaplan–Meier method and Cox regression analysis were conducted to evaluate the prognostic value of SKA3. Gene set enrichment analysis (GSEA) was performed to screen biological pathways using the TCGA dataset. Besides, single sample gene set enrichment analysis (ssGSEA) was utilized to identify immune infiltration cells about SKA3. RESULTS: SKA3 mRNA was expressed at high levels in breast cancer tissues compared with normal tissues. Chi-square test and Fisher’s exact test showed SKA3 expression was related to age, tumor (T) classification, node (N) classification, tumor-node-metastasis (TNM) stage, estrogen receptor (ER), progesterone receptor (PR), molecular subtype, and race. RT-qPCR results showed that SKA3 expression was overexpressed in ER, PR status, and molecular subtype in Chinese people. Kaplan–Meier curves implicated that high SKA3 expression was related to a poor prognosis in female early breast cancer patients. Cox regression models showed that high SKA3 expression could be used as an independent risk factor for female early breast cancer. Four signaling pathways were enriched in the high SKA3 expression group, including mTORC1 signaling pathway, MYC targets v1, mitotic spindle, estrogen response early. Besides, the SKA3 expression level was associate with infiltrating levels of activated CD4 T cells and eosinophils in breast cancer. CONCLUSION: High SKA3 expression correlates with poor prognosis and immune infiltrates in breast cancer. SKA3 may become a biomarker for the prognosis of breast cancer.
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spelling pubmed-86752622022-01-05 Overexpression of SKA3 correlates with poor prognosis in female early breast cancer Zhong, Yue Zhuang, Zhenjie Mo, Peiju Lin, Mandi Gong, Jiaqian Huang, Jiarong Mo, Haiyan Lu, Yuyun Huang, Mei PeerJ Bioinformatics BACKGROUND: Spindle and kinetochore associated complex subunit 3 (SKA3) plays an important role in tumorigenesis and the progression of various tumors. But the relationship between SKA3 and early breast cancer remains unclear. The study aimed to explore the prognostic significance of SKA3 in breast cancer. METHODS: In the study, SKA3 expression was initially assessed using the Oncomine database and The Cancer Genome Atlas database (TCGA). Then, we presented validation results for RT-qPCR (quantitative reverse transcription PCR) and ELISA (enzyme-linked immunosorbent assay). The relationship between clinical characteristics and SKA3 expression was assessed by Chi-square test and Fisher’s exact test. Kaplan–Meier method and Cox regression analysis were conducted to evaluate the prognostic value of SKA3. Gene set enrichment analysis (GSEA) was performed to screen biological pathways using the TCGA dataset. Besides, single sample gene set enrichment analysis (ssGSEA) was utilized to identify immune infiltration cells about SKA3. RESULTS: SKA3 mRNA was expressed at high levels in breast cancer tissues compared with normal tissues. Chi-square test and Fisher’s exact test showed SKA3 expression was related to age, tumor (T) classification, node (N) classification, tumor-node-metastasis (TNM) stage, estrogen receptor (ER), progesterone receptor (PR), molecular subtype, and race. RT-qPCR results showed that SKA3 expression was overexpressed in ER, PR status, and molecular subtype in Chinese people. Kaplan–Meier curves implicated that high SKA3 expression was related to a poor prognosis in female early breast cancer patients. Cox regression models showed that high SKA3 expression could be used as an independent risk factor for female early breast cancer. Four signaling pathways were enriched in the high SKA3 expression group, including mTORC1 signaling pathway, MYC targets v1, mitotic spindle, estrogen response early. Besides, the SKA3 expression level was associate with infiltrating levels of activated CD4 T cells and eosinophils in breast cancer. CONCLUSION: High SKA3 expression correlates with poor prognosis and immune infiltrates in breast cancer. SKA3 may become a biomarker for the prognosis of breast cancer. PeerJ Inc. 2021-12-13 /pmc/articles/PMC8675262/ /pubmed/34993016 http://dx.doi.org/10.7717/peerj.12506 Text en © 2021 Zhong et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited.
spellingShingle Bioinformatics
Zhong, Yue
Zhuang, Zhenjie
Mo, Peiju
Lin, Mandi
Gong, Jiaqian
Huang, Jiarong
Mo, Haiyan
Lu, Yuyun
Huang, Mei
Overexpression of SKA3 correlates with poor prognosis in female early breast cancer
title Overexpression of SKA3 correlates with poor prognosis in female early breast cancer
title_full Overexpression of SKA3 correlates with poor prognosis in female early breast cancer
title_fullStr Overexpression of SKA3 correlates with poor prognosis in female early breast cancer
title_full_unstemmed Overexpression of SKA3 correlates with poor prognosis in female early breast cancer
title_short Overexpression of SKA3 correlates with poor prognosis in female early breast cancer
title_sort overexpression of ska3 correlates with poor prognosis in female early breast cancer
topic Bioinformatics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8675262/
https://www.ncbi.nlm.nih.gov/pubmed/34993016
http://dx.doi.org/10.7717/peerj.12506
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