Comprehensive analysis of ESCRT transcriptome-associated signatures and identification of the regulatory role of LMO7-AS1 in osteosarcoma

Abstract Osteosarcoma (OS) is a commonly observed malignant tumor in orthopedics that has a very poor prognosis. The endosomal sorting complex required for transport (ESCRT) is important for the development and progression of cancer and may be a significant target for cancer therapy. First, we built...

Full description

Saved in:
Bibliographic Details
Main Authors: Shibing Zhao, Dasheng Tian, Fei Huang, Lei Wang, Jinhao Cheng, Zhitao He, Qitian Shen, Shuai Liang, Deliang Gong, Jun Liu, Chengfeng Yi, Chun Zhang, Erbao Bian, Juehua Jing, Tao Wang
Format: Article
Language:English
Published: BMC 2025-01-01
Series:Cancer Cell International
Subjects:
Online Access:https://doi.org/10.1186/s12935-025-03659-4
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1832571347919699968
author Shibing Zhao
Dasheng Tian
Fei Huang
Lei Wang
Jinhao Cheng
Zhitao He
Qitian Shen
Shuai Liang
Deliang Gong
Jun Liu
Chengfeng Yi
Chun Zhang
Erbao Bian
Juehua Jing
Tao Wang
author_facet Shibing Zhao
Dasheng Tian
Fei Huang
Lei Wang
Jinhao Cheng
Zhitao He
Qitian Shen
Shuai Liang
Deliang Gong
Jun Liu
Chengfeng Yi
Chun Zhang
Erbao Bian
Juehua Jing
Tao Wang
author_sort Shibing Zhao
collection DOAJ
description Abstract Osteosarcoma (OS) is a commonly observed malignant tumor in orthopedics that has a very poor prognosis. The endosomal sorting complex required for transport (ESCRT) is important for the development and progression of cancer and may be a significant target for cancer therapy. First, we built a prognostic signature using 7 ESCRT-related genes (ERGs) to predict OS patient prognosis. Analysis of internal and external datasets revealed that the ERG signature has good predictive ability and reproducibility. Immune analysis demonstrated a significant correlation between OS patient immune status and ERG signature score. Moreover, ERG signature score was found to be associated with the response of OS patients to immunotherapy and anticancer drugs. Additionally, we constructed a prognostic signature consisting of 10 ESCRT-related long noncoding RNAs (ERLs) that effectively predicted the prognosis of OS patients. Furthermore, two subgroups of OS patients with distinct prognoses (clusters 1 and 2) were identified. Finally, LMO7-AS1 was chosen for functional experimental validation. The knockdown of LMO7-AS1 suppressed the malignant progression of OS cells. Furthermore, transcriptome sequencing was performed on OS cells and revealed a correlation between LMO7-AS1 and the PI3K-Akt signaling pathway. In conclusion, our ESCRT transcriptome-associated signatures can act as prognostic biomarkers for OS, and LMO7-AS1 is a novel therapeutic target for the treatment of OS.
format Article
id doaj-art-fb8e497162264e9a8dcc7a343f7ec690
institution Kabale University
issn 1475-2867
language English
publishDate 2025-01-01
publisher BMC
record_format Article
series Cancer Cell International
spelling doaj-art-fb8e497162264e9a8dcc7a343f7ec6902025-02-02T12:43:22ZengBMCCancer Cell International1475-28672025-01-0125111710.1186/s12935-025-03659-4Comprehensive analysis of ESCRT transcriptome-associated signatures and identification of the regulatory role of LMO7-AS1 in osteosarcomaShibing Zhao0Dasheng Tian1Fei Huang2Lei Wang3Jinhao Cheng4Zhitao He5Qitian Shen6Shuai Liang7Deliang Gong8Jun Liu9Chengfeng Yi10Chun Zhang11Erbao Bian12Juehua Jing13Tao Wang14Department of Orthopaedics, The Second Affiliated Hospital of Anhui Medical UniversityDepartment of Orthopaedics, The Second Affiliated Hospital of Anhui Medical UniversityDepartment of Orthopaedics, The Second Affiliated Hospital of Anhui Medical UniversityDepartment of Orthopaedics, Division of Life Sciences and Medicine, The First Affiliated Hospital of USTC, University of Science and Technology of ChinaDepartment of Orthopaedics, The Second Affiliated Hospital of Anhui Medical UniversityDepartment of Orthopaedics, The Second Affiliated Hospital of Anhui Medical UniversityDepartment of Orthopaedics, The Second Affiliated Hospital of Anhui Medical UniversityDepartment of Orthopaedics, The Second Affiliated Hospital of Anhui Medical UniversityDepartment of Orthopaedics, The Second Affiliated Hospital of Anhui Medical UniversityDepartment of Orthopaedics, The Second Affiliated Hospital of Anhui Medical UniversityDepartment of Orthopaedics, The Second Affiliated Hospital of Anhui Medical UniversityDepartment of Orthopaedics, The Second Affiliated Hospital of Anhui Medical UniversityDepartment of Orthopaedics, The Second Affiliated Hospital of Anhui Medical UniversityDepartment of Orthopaedics, The Second Affiliated Hospital of Anhui Medical UniversityDepartment of Orthopaedics, The Second Affiliated Hospital of Anhui Medical UniversityAbstract Osteosarcoma (OS) is a commonly observed malignant tumor in orthopedics that has a very poor prognosis. The endosomal sorting complex required for transport (ESCRT) is important for the development and progression of cancer and may be a significant target for cancer therapy. First, we built a prognostic signature using 7 ESCRT-related genes (ERGs) to predict OS patient prognosis. Analysis of internal and external datasets revealed that the ERG signature has good predictive ability and reproducibility. Immune analysis demonstrated a significant correlation between OS patient immune status and ERG signature score. Moreover, ERG signature score was found to be associated with the response of OS patients to immunotherapy and anticancer drugs. Additionally, we constructed a prognostic signature consisting of 10 ESCRT-related long noncoding RNAs (ERLs) that effectively predicted the prognosis of OS patients. Furthermore, two subgroups of OS patients with distinct prognoses (clusters 1 and 2) were identified. Finally, LMO7-AS1 was chosen for functional experimental validation. The knockdown of LMO7-AS1 suppressed the malignant progression of OS cells. Furthermore, transcriptome sequencing was performed on OS cells and revealed a correlation between LMO7-AS1 and the PI3K-Akt signaling pathway. In conclusion, our ESCRT transcriptome-associated signatures can act as prognostic biomarkers for OS, and LMO7-AS1 is a novel therapeutic target for the treatment of OS.https://doi.org/10.1186/s12935-025-03659-4OsteosarcomaESCRTSignaturePrognosisImmune
spellingShingle Shibing Zhao
Dasheng Tian
Fei Huang
Lei Wang
Jinhao Cheng
Zhitao He
Qitian Shen
Shuai Liang
Deliang Gong
Jun Liu
Chengfeng Yi
Chun Zhang
Erbao Bian
Juehua Jing
Tao Wang
Comprehensive analysis of ESCRT transcriptome-associated signatures and identification of the regulatory role of LMO7-AS1 in osteosarcoma
Cancer Cell International
Osteosarcoma
ESCRT
Signature
Prognosis
Immune
title Comprehensive analysis of ESCRT transcriptome-associated signatures and identification of the regulatory role of LMO7-AS1 in osteosarcoma
title_full Comprehensive analysis of ESCRT transcriptome-associated signatures and identification of the regulatory role of LMO7-AS1 in osteosarcoma
title_fullStr Comprehensive analysis of ESCRT transcriptome-associated signatures and identification of the regulatory role of LMO7-AS1 in osteosarcoma
title_full_unstemmed Comprehensive analysis of ESCRT transcriptome-associated signatures and identification of the regulatory role of LMO7-AS1 in osteosarcoma
title_short Comprehensive analysis of ESCRT transcriptome-associated signatures and identification of the regulatory role of LMO7-AS1 in osteosarcoma
title_sort comprehensive analysis of escrt transcriptome associated signatures and identification of the regulatory role of lmo7 as1 in osteosarcoma
topic Osteosarcoma
ESCRT
Signature
Prognosis
Immune
url https://doi.org/10.1186/s12935-025-03659-4
work_keys_str_mv AT shibingzhao comprehensiveanalysisofescrttranscriptomeassociatedsignaturesandidentificationoftheregulatoryroleoflmo7as1inosteosarcoma
AT dashengtian comprehensiveanalysisofescrttranscriptomeassociatedsignaturesandidentificationoftheregulatoryroleoflmo7as1inosteosarcoma
AT feihuang comprehensiveanalysisofescrttranscriptomeassociatedsignaturesandidentificationoftheregulatoryroleoflmo7as1inosteosarcoma
AT leiwang comprehensiveanalysisofescrttranscriptomeassociatedsignaturesandidentificationoftheregulatoryroleoflmo7as1inosteosarcoma
AT jinhaocheng comprehensiveanalysisofescrttranscriptomeassociatedsignaturesandidentificationoftheregulatoryroleoflmo7as1inosteosarcoma
AT zhitaohe comprehensiveanalysisofescrttranscriptomeassociatedsignaturesandidentificationoftheregulatoryroleoflmo7as1inosteosarcoma
AT qitianshen comprehensiveanalysisofescrttranscriptomeassociatedsignaturesandidentificationoftheregulatoryroleoflmo7as1inosteosarcoma
AT shuailiang comprehensiveanalysisofescrttranscriptomeassociatedsignaturesandidentificationoftheregulatoryroleoflmo7as1inosteosarcoma
AT delianggong comprehensiveanalysisofescrttranscriptomeassociatedsignaturesandidentificationoftheregulatoryroleoflmo7as1inosteosarcoma
AT junliu comprehensiveanalysisofescrttranscriptomeassociatedsignaturesandidentificationoftheregulatoryroleoflmo7as1inosteosarcoma
AT chengfengyi comprehensiveanalysisofescrttranscriptomeassociatedsignaturesandidentificationoftheregulatoryroleoflmo7as1inosteosarcoma
AT chunzhang comprehensiveanalysisofescrttranscriptomeassociatedsignaturesandidentificationoftheregulatoryroleoflmo7as1inosteosarcoma
AT erbaobian comprehensiveanalysisofescrttranscriptomeassociatedsignaturesandidentificationoftheregulatoryroleoflmo7as1inosteosarcoma
AT juehuajing comprehensiveanalysisofescrttranscriptomeassociatedsignaturesandidentificationoftheregulatoryroleoflmo7as1inosteosarcoma
AT taowang comprehensiveanalysisofescrttranscriptomeassociatedsignaturesandidentificationoftheregulatoryroleoflmo7as1inosteosarcoma