Role of exosome-mediated molecules SNORD91A and SLC40A1 in M2 macrophage polarization and prognosis of ESCC

Abstract Background Exosome-mediated interaction serves as a significant regulatory factor for M2 macrophage polarization in cancer. Methods All accessible data were acquired from The Cancer Genome Atlas (TCGA) database and analyzed using R software. Molecules implicated in exocrine secretion were a...

Full description

Bibliographic Details
Main Authors: Yang Xue, Zhengyan Cheng, Yida Liao, Xing Chen
Format: Article
Language:English
Published: Springer 2023-09-01
Series:Discover Oncology
Subjects:
Online Access:https://doi.org/10.1007/s12672-023-00797-x
_version_ 1797558798067433472
author Yang Xue
Zhengyan Cheng
Yida Liao
Xing Chen
author_facet Yang Xue
Zhengyan Cheng
Yida Liao
Xing Chen
author_sort Yang Xue
collection DOAJ
description Abstract Background Exosome-mediated interaction serves as a significant regulatory factor for M2 macrophage polarization in cancer. Methods All accessible data were acquired from The Cancer Genome Atlas (TCGA) database and analyzed using R software. Molecules implicated in exocrine secretion were amassed from the ExoCarta database. Our research initially quantified the immune microenvironment in Esophageal Squamous Cell Carcinoma (ESCC) patients based on the expression profile sourced from the TCGA database. Additionally, we delved into the biological role of M2 macrophages in ESCC via Gene Set Enrichment Analysis (GSEA). Results We observed that patients with high M2 macrophage infiltration typically have a poorer prognosis. Subsequently, a total of 1457 molecules were identified, with 103 of these molecules believed to function through exocrine mechanisms, as supported by data from the ExoCarta database. SNORD91A and SLC40A1 were ultimately pinpointed due to their correlation with patient prognosis. Moreover, we investigated their potential roles in ESCC, including biological enrichment, immune infiltration, and genomic instability analysis. Conclusions Our study identified exosome-associated molecules, namely SNORD91A and SLC40A1, which notably impact ESCC prognosis and local M2 macrophage recruitment, thereby presenting potential therapeutic targets for ESCC.
first_indexed 2024-03-10T17:36:28Z
format Article
id doaj.art-544f90283b0b4937987bc4a9c2366d30
institution Directory Open Access Journal
issn 2730-6011
language English
last_indexed 2024-03-10T17:36:28Z
publishDate 2023-09-01
publisher Springer
record_format Article
series Discover Oncology
spelling doaj.art-544f90283b0b4937987bc4a9c2366d302023-11-20T09:50:27ZengSpringerDiscover Oncology2730-60112023-09-0114111110.1007/s12672-023-00797-xRole of exosome-mediated molecules SNORD91A and SLC40A1 in M2 macrophage polarization and prognosis of ESCCYang Xue0Zhengyan Cheng1Yida Liao2Xing Chen3Department of Thoracic Surgery, Sichuan Academy of Medical Sciences & Sichuan Provincial People’s HospitalDepartment of Pathology, Sichuan Academy of Medical Science & Sichuan Provincial People’s HospitalDepartment of Thoracic Surgery, Sichuan Academy of Medical Sciences & Sichuan Provincial People’s HospitalDepartment of Thoracic Surgery, Sichuan Academy of Medical Sciences & Sichuan Provincial People’s HospitalAbstract Background Exosome-mediated interaction serves as a significant regulatory factor for M2 macrophage polarization in cancer. Methods All accessible data were acquired from The Cancer Genome Atlas (TCGA) database and analyzed using R software. Molecules implicated in exocrine secretion were amassed from the ExoCarta database. Our research initially quantified the immune microenvironment in Esophageal Squamous Cell Carcinoma (ESCC) patients based on the expression profile sourced from the TCGA database. Additionally, we delved into the biological role of M2 macrophages in ESCC via Gene Set Enrichment Analysis (GSEA). Results We observed that patients with high M2 macrophage infiltration typically have a poorer prognosis. Subsequently, a total of 1457 molecules were identified, with 103 of these molecules believed to function through exocrine mechanisms, as supported by data from the ExoCarta database. SNORD91A and SLC40A1 were ultimately pinpointed due to their correlation with patient prognosis. Moreover, we investigated their potential roles in ESCC, including biological enrichment, immune infiltration, and genomic instability analysis. Conclusions Our study identified exosome-associated molecules, namely SNORD91A and SLC40A1, which notably impact ESCC prognosis and local M2 macrophage recruitment, thereby presenting potential therapeutic targets for ESCC.https://doi.org/10.1007/s12672-023-00797-xESCCExosomesM2 Macrophage PolarizationSNORD91ASLC40A1
spellingShingle Yang Xue
Zhengyan Cheng
Yida Liao
Xing Chen
Role of exosome-mediated molecules SNORD91A and SLC40A1 in M2 macrophage polarization and prognosis of ESCC
Discover Oncology
ESCC
Exosomes
M2 Macrophage Polarization
SNORD91A
SLC40A1
title Role of exosome-mediated molecules SNORD91A and SLC40A1 in M2 macrophage polarization and prognosis of ESCC
title_full Role of exosome-mediated molecules SNORD91A and SLC40A1 in M2 macrophage polarization and prognosis of ESCC
title_fullStr Role of exosome-mediated molecules SNORD91A and SLC40A1 in M2 macrophage polarization and prognosis of ESCC
title_full_unstemmed Role of exosome-mediated molecules SNORD91A and SLC40A1 in M2 macrophage polarization and prognosis of ESCC
title_short Role of exosome-mediated molecules SNORD91A and SLC40A1 in M2 macrophage polarization and prognosis of ESCC
title_sort role of exosome mediated molecules snord91a and slc40a1 in m2 macrophage polarization and prognosis of escc
topic ESCC
Exosomes
M2 Macrophage Polarization
SNORD91A
SLC40A1
url https://doi.org/10.1007/s12672-023-00797-x
work_keys_str_mv AT yangxue roleofexosomemediatedmoleculessnord91aandslc40a1inm2macrophagepolarizationandprognosisofescc
AT zhengyancheng roleofexosomemediatedmoleculessnord91aandslc40a1inm2macrophagepolarizationandprognosisofescc
AT yidaliao roleofexosomemediatedmoleculessnord91aandslc40a1inm2macrophagepolarizationandprognosisofescc
AT xingchen roleofexosomemediatedmoleculessnord91aandslc40a1inm2macrophagepolarizationandprognosisofescc