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The correlation and role analysis of SLC30A1 and SLC30A10 in cervical carcinoma

Background: SLC30 family genes, also known as ZnT family genes, can keep cellular zinc levels within a physiological range by exporting zinc to extracellular space or by isolating zinc in the specific regions of cytoplasm when cellular zinc concentrations are elevated in human cells. There are growi...

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Autores principales: Zhang, Jing, Chen, Xin-Wei, Shu, Li-Sha, Liu, Chong-Dong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8824890/
https://www.ncbi.nlm.nih.gov/pubmed/35154468
http://dx.doi.org/10.7150/jca.56777
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author Zhang, Jing
Chen, Xin-Wei
Shu, Li-Sha
Liu, Chong-Dong
author_facet Zhang, Jing
Chen, Xin-Wei
Shu, Li-Sha
Liu, Chong-Dong
author_sort Zhang, Jing
collection PubMed
description Background: SLC30 family genes, also known as ZnT family genes, can keep cellular zinc levels within a physiological range by exporting zinc to extracellular space or by isolating zinc in the specific regions of cytoplasm when cellular zinc concentrations are elevated in human cells. There are growing evidences that dysregulated expression of SLC30 family genes can potentially influence tumorigenesis. However, the expression and prognostic value of SLC30 family genes in cervical carcinoma are poorly characterized. Methods: In this study, we used many tools such as UALCAN, Kaplan-Meier Plotter, cBioPortal, LinkedOmics, FunRich, Metascape, GeneMANIA, Open targets and TISIDB to perform bioinformatics analysis of SLC30 family genes in cervical carcinoma. Results: We found that the expression of SLC30A1/7/10 was significantly higher in cervical carcinoma than that in normal matched tissues, while SLC30A2/8 mRNA levels were decreased compared to normal tissues. For tumor stages, SLC30A1, SLC30A7 and SLC30A10 groups significantly varied. And a high expression of SLC30A1, SLC30A6, SLC30A8 and SLC30A10 was associated with worse overall survival in cervical carcinoma patients. Besides, we found that SLC30A1/10 may have a potential regulatory role in immune infiltration in cervical carcinoma. In addition, the results showed that the high expression of SLC30A1 was resistant to 79 drugs or small molecules; Two drugs (Neopeltolide and Tozasertib) can inhibit the high expression of SLC30A10 in cancers. Conclusion: SLC30A1 and SLC30A10 can be recognized as potential diagnostic indicators and therapeutic targets in cervical carcinoma.
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spelling pubmed-88248902022-02-11 The correlation and role analysis of SLC30A1 and SLC30A10 in cervical carcinoma Zhang, Jing Chen, Xin-Wei Shu, Li-Sha Liu, Chong-Dong J Cancer Research Paper Background: SLC30 family genes, also known as ZnT family genes, can keep cellular zinc levels within a physiological range by exporting zinc to extracellular space or by isolating zinc in the specific regions of cytoplasm when cellular zinc concentrations are elevated in human cells. There are growing evidences that dysregulated expression of SLC30 family genes can potentially influence tumorigenesis. However, the expression and prognostic value of SLC30 family genes in cervical carcinoma are poorly characterized. Methods: In this study, we used many tools such as UALCAN, Kaplan-Meier Plotter, cBioPortal, LinkedOmics, FunRich, Metascape, GeneMANIA, Open targets and TISIDB to perform bioinformatics analysis of SLC30 family genes in cervical carcinoma. Results: We found that the expression of SLC30A1/7/10 was significantly higher in cervical carcinoma than that in normal matched tissues, while SLC30A2/8 mRNA levels were decreased compared to normal tissues. For tumor stages, SLC30A1, SLC30A7 and SLC30A10 groups significantly varied. And a high expression of SLC30A1, SLC30A6, SLC30A8 and SLC30A10 was associated with worse overall survival in cervical carcinoma patients. Besides, we found that SLC30A1/10 may have a potential regulatory role in immune infiltration in cervical carcinoma. In addition, the results showed that the high expression of SLC30A1 was resistant to 79 drugs or small molecules; Two drugs (Neopeltolide and Tozasertib) can inhibit the high expression of SLC30A10 in cancers. Conclusion: SLC30A1 and SLC30A10 can be recognized as potential diagnostic indicators and therapeutic targets in cervical carcinoma. Ivyspring International Publisher 2022-01-04 /pmc/articles/PMC8824890/ /pubmed/35154468 http://dx.doi.org/10.7150/jca.56777 Text en © The author(s) 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/). See http://ivyspring.com/terms for full terms and conditions.
spellingShingle Research Paper
Zhang, Jing
Chen, Xin-Wei
Shu, Li-Sha
Liu, Chong-Dong
The correlation and role analysis of SLC30A1 and SLC30A10 in cervical carcinoma
title The correlation and role analysis of SLC30A1 and SLC30A10 in cervical carcinoma
title_full The correlation and role analysis of SLC30A1 and SLC30A10 in cervical carcinoma
title_fullStr The correlation and role analysis of SLC30A1 and SLC30A10 in cervical carcinoma
title_full_unstemmed The correlation and role analysis of SLC30A1 and SLC30A10 in cervical carcinoma
title_short The correlation and role analysis of SLC30A1 and SLC30A10 in cervical carcinoma
title_sort correlation and role analysis of slc30a1 and slc30a10 in cervical carcinoma
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8824890/
https://www.ncbi.nlm.nih.gov/pubmed/35154468
http://dx.doi.org/10.7150/jca.56777
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