Cargando…

SLC25A1-associated prognostic signature predicts poor survival in acute myeloid leukemia patients

Background: Acute myeloid leukemia (AML) is a heterogeneous malignant disease. SLC25A1, the gene encoding mitochondrial carrier subfamily of solute carrier proteins, was reported to be overexpressed in certain solid tumors. However, its expression and value as prognostic marker has not been assessed...

Descripción completa

Detalles Bibliográficos
Autores principales: Liu, Fangshu, Deng, Suqi, Li, Yue, Du, Juan, Zeng, Hui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9852877/
https://www.ncbi.nlm.nih.gov/pubmed/36685828
http://dx.doi.org/10.3389/fgene.2022.1081262
_version_ 1784872759552114688
author Liu, Fangshu
Deng, Suqi
Li, Yue
Du, Juan
Zeng, Hui
author_facet Liu, Fangshu
Deng, Suqi
Li, Yue
Du, Juan
Zeng, Hui
author_sort Liu, Fangshu
collection PubMed
description Background: Acute myeloid leukemia (AML) is a heterogeneous malignant disease. SLC25A1, the gene encoding mitochondrial carrier subfamily of solute carrier proteins, was reported to be overexpressed in certain solid tumors. However, its expression and value as prognostic marker has not been assessed in AML. Methods: We retrieved RNA profile and corresponding clinical data of AML patients from the Beat AML, TCGA, and TARGET databases (TARGET_AML). Patients in the TCGA cohort were well-grouped into two group based on SLC25A1 and differentially expressed genes were determined between the SLC25A1 high and low group. The expression of SLC25A1 was validated with clinical samples. The survival and apoptosis of two AML cell lines were analyzed with SLC25A1 inhibitor (CTPI-2) treatment. Cox and the least absolute shrinkage and selection operator (LASSO) regression analyses were applied to Beat AML database to identify SLC25A1-associated genes for the construction of a prognostic risk-scoring model. Survival analysis was performed by Kaplan-Meier and receiver operator characteristic curves. Results: Our analysis revealed that high expressed level of SLC25A1 in AML patients correlates with unfavorable prognosis. Moreover, SLC25A1 expression was positively associated with metabolism activity. We further demonstrated that the inhibition of SLC25A1 could inhibit the proliferation and increase the apoptosis of AML cells. In addition, a panel of SLC25A1-associated genes, was identified to construct a prognostic risk-scoring model. This SLC25A1-associated prognostic signature (SPS) is an independent risk factor with high area under curve (AUC) values of receiver operating characteristic (ROC) curves. A high SPS in leukemia patients is associated with poor survival. A Prognostic nomogram including the SPS and other clinical parameters, was constructed and its predictive efficiency was confirmed. Conclusion: We have successfully established a SPS prognostic model that predict outcome and risk stratification in AML. This risk model can be used as an independent biomarker to assess prognosis of AML.
format Online
Article
Text
id pubmed-9852877
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-98528772023-01-21 SLC25A1-associated prognostic signature predicts poor survival in acute myeloid leukemia patients Liu, Fangshu Deng, Suqi Li, Yue Du, Juan Zeng, Hui Front Genet Genetics Background: Acute myeloid leukemia (AML) is a heterogeneous malignant disease. SLC25A1, the gene encoding mitochondrial carrier subfamily of solute carrier proteins, was reported to be overexpressed in certain solid tumors. However, its expression and value as prognostic marker has not been assessed in AML. Methods: We retrieved RNA profile and corresponding clinical data of AML patients from the Beat AML, TCGA, and TARGET databases (TARGET_AML). Patients in the TCGA cohort were well-grouped into two group based on SLC25A1 and differentially expressed genes were determined between the SLC25A1 high and low group. The expression of SLC25A1 was validated with clinical samples. The survival and apoptosis of two AML cell lines were analyzed with SLC25A1 inhibitor (CTPI-2) treatment. Cox and the least absolute shrinkage and selection operator (LASSO) regression analyses were applied to Beat AML database to identify SLC25A1-associated genes for the construction of a prognostic risk-scoring model. Survival analysis was performed by Kaplan-Meier and receiver operator characteristic curves. Results: Our analysis revealed that high expressed level of SLC25A1 in AML patients correlates with unfavorable prognosis. Moreover, SLC25A1 expression was positively associated with metabolism activity. We further demonstrated that the inhibition of SLC25A1 could inhibit the proliferation and increase the apoptosis of AML cells. In addition, a panel of SLC25A1-associated genes, was identified to construct a prognostic risk-scoring model. This SLC25A1-associated prognostic signature (SPS) is an independent risk factor with high area under curve (AUC) values of receiver operating characteristic (ROC) curves. A high SPS in leukemia patients is associated with poor survival. A Prognostic nomogram including the SPS and other clinical parameters, was constructed and its predictive efficiency was confirmed. Conclusion: We have successfully established a SPS prognostic model that predict outcome and risk stratification in AML. This risk model can be used as an independent biomarker to assess prognosis of AML. Frontiers Media S.A. 2023-01-06 /pmc/articles/PMC9852877/ /pubmed/36685828 http://dx.doi.org/10.3389/fgene.2022.1081262 Text en Copyright © 2023 Liu, Deng, Li, Du and Zeng. 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 Genetics
Liu, Fangshu
Deng, Suqi
Li, Yue
Du, Juan
Zeng, Hui
SLC25A1-associated prognostic signature predicts poor survival in acute myeloid leukemia patients
title SLC25A1-associated prognostic signature predicts poor survival in acute myeloid leukemia patients
title_full SLC25A1-associated prognostic signature predicts poor survival in acute myeloid leukemia patients
title_fullStr SLC25A1-associated prognostic signature predicts poor survival in acute myeloid leukemia patients
title_full_unstemmed SLC25A1-associated prognostic signature predicts poor survival in acute myeloid leukemia patients
title_short SLC25A1-associated prognostic signature predicts poor survival in acute myeloid leukemia patients
title_sort slc25a1-associated prognostic signature predicts poor survival in acute myeloid leukemia patients
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9852877/
https://www.ncbi.nlm.nih.gov/pubmed/36685828
http://dx.doi.org/10.3389/fgene.2022.1081262
work_keys_str_mv AT liufangshu slc25a1associatedprognosticsignaturepredictspoorsurvivalinacutemyeloidleukemiapatients
AT dengsuqi slc25a1associatedprognosticsignaturepredictspoorsurvivalinacutemyeloidleukemiapatients
AT liyue slc25a1associatedprognosticsignaturepredictspoorsurvivalinacutemyeloidleukemiapatients
AT dujuan slc25a1associatedprognosticsignaturepredictspoorsurvivalinacutemyeloidleukemiapatients
AT zenghui slc25a1associatedprognosticsignaturepredictspoorsurvivalinacutemyeloidleukemiapatients