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S100 family members: potential therapeutic target in patients with hepatocellular carcinoma: A STROBE study
Proteins in S100 family exhibit different expressions patterns and perform different cytological functions, playing substantial roles in certain cancers, carcinogenesis, and disease progression. However, the expression and role of S100 family members in the prognosis of hepatocellular carcinoma (HCC...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7837992/ https://www.ncbi.nlm.nih.gov/pubmed/33546025 http://dx.doi.org/10.1097/MD.0000000000024135 |
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author | Zhang, Cai Yao, Rucheng Chen, Jie Zou, Qiong Zeng, Linghai |
author_facet | Zhang, Cai Yao, Rucheng Chen, Jie Zou, Qiong Zeng, Linghai |
author_sort | Zhang, Cai |
collection | PubMed |
description | Proteins in S100 family exhibit different expressions patterns and perform different cytological functions, playing substantial roles in certain cancers, carcinogenesis, and disease progression. However, the expression and role of S100 family members in the prognosis of hepatocellular carcinoma (HCC) remains unclear. To investigate the effect of S100 family members for the prognosis of liver cancer, we assessed overall survival (OS) using a Kaplan–Meier plotter (KM plotter) in liver cancer patients with different situation. Our results showed that 15 members of the S100 family exhibited high levels of expression and these levels were correlated with OS in liver cancer patients. The higher expression of S100A5, S100A7, S100A7A, S100A12, S100Z, and S100G was reflected with better survival in liver cancer patients. However, worse prognosis was related to higher levels of expression of S100A2, S100A6, S100A8, S100A9, S100A10, S100A11, S10013, S100A14, and S100P. We then evaluated the prognostic values of S100 family members expression for evaluating different stages of AJCC-T, vascular invasion, alcohol consumption, and the presence of hepatitis virus in liver cancer patients. Lastly, we studied the prognostic values of S100 family members expression for patients after sorafenib treatment. In conclusion, our findings show that the proteins of S100 family members exhibit differential expression and may be useful as targets for liver cancer, facilitating novel diagnostic and therapeutic strategies in cancer. |
format | Online Article Text |
id | pubmed-7837992 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-78379922021-01-28 S100 family members: potential therapeutic target in patients with hepatocellular carcinoma: A STROBE study Zhang, Cai Yao, Rucheng Chen, Jie Zou, Qiong Zeng, Linghai Medicine (Baltimore) 5700 Proteins in S100 family exhibit different expressions patterns and perform different cytological functions, playing substantial roles in certain cancers, carcinogenesis, and disease progression. However, the expression and role of S100 family members in the prognosis of hepatocellular carcinoma (HCC) remains unclear. To investigate the effect of S100 family members for the prognosis of liver cancer, we assessed overall survival (OS) using a Kaplan–Meier plotter (KM plotter) in liver cancer patients with different situation. Our results showed that 15 members of the S100 family exhibited high levels of expression and these levels were correlated with OS in liver cancer patients. The higher expression of S100A5, S100A7, S100A7A, S100A12, S100Z, and S100G was reflected with better survival in liver cancer patients. However, worse prognosis was related to higher levels of expression of S100A2, S100A6, S100A8, S100A9, S100A10, S100A11, S10013, S100A14, and S100P. We then evaluated the prognostic values of S100 family members expression for evaluating different stages of AJCC-T, vascular invasion, alcohol consumption, and the presence of hepatitis virus in liver cancer patients. Lastly, we studied the prognostic values of S100 family members expression for patients after sorafenib treatment. In conclusion, our findings show that the proteins of S100 family members exhibit differential expression and may be useful as targets for liver cancer, facilitating novel diagnostic and therapeutic strategies in cancer. Lippincott Williams & Wilkins 2021-01-22 /pmc/articles/PMC7837992/ /pubmed/33546025 http://dx.doi.org/10.1097/MD.0000000000024135 Text en Copyright © 2021 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by-nc/4.0 This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial License 4.0 (CCBY-NC), where it is permissible to download, share, remix, transform, and buildup the work provided it is properly cited. The work cannot be used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc/4.0 |
spellingShingle | 5700 Zhang, Cai Yao, Rucheng Chen, Jie Zou, Qiong Zeng, Linghai S100 family members: potential therapeutic target in patients with hepatocellular carcinoma: A STROBE study |
title | S100 family members: potential therapeutic target in patients with hepatocellular carcinoma: A STROBE study |
title_full | S100 family members: potential therapeutic target in patients with hepatocellular carcinoma: A STROBE study |
title_fullStr | S100 family members: potential therapeutic target in patients with hepatocellular carcinoma: A STROBE study |
title_full_unstemmed | S100 family members: potential therapeutic target in patients with hepatocellular carcinoma: A STROBE study |
title_short | S100 family members: potential therapeutic target in patients with hepatocellular carcinoma: A STROBE study |
title_sort | s100 family members: potential therapeutic target in patients with hepatocellular carcinoma: a strobe study |
topic | 5700 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7837992/ https://www.ncbi.nlm.nih.gov/pubmed/33546025 http://dx.doi.org/10.1097/MD.0000000000024135 |
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