Characterization of the gene signature correlated with favorable response to chemoradiotherapy in rectal cancer: A hypothesis‐generating study

Abstract Purpose This study aimed to define the gene signature associated with response to neoadjuvant chemoradiotherapy (nCRT), or chemoradiosensitivity (CRS) signature, in rectal cancer, and investigate the correlation between the CRS signature and characteristics of tumor. Materials and Methods T...

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Main Authors: Seung Hyuck Jeon, Eui Kyu Chie
Format: Article
Language:English
Published: Wiley 2023-04-01
Series:Cancer Medicine
Subjects:
Online Access:https://doi.org/10.1002/cam4.5586
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author Seung Hyuck Jeon
Eui Kyu Chie
author_facet Seung Hyuck Jeon
Eui Kyu Chie
author_sort Seung Hyuck Jeon
collection DOAJ
description Abstract Purpose This study aimed to define the gene signature associated with response to neoadjuvant chemoradiotherapy (nCRT), or chemoradiosensitivity (CRS) signature, in rectal cancer, and investigate the correlation between the CRS signature and characteristics of tumor. Materials and Methods Three public microarray datasets of pre‐nCRT rectal cancer were used to discover and validate the CRS signature, and the pathway analysis of the CRS signature was performed. Patients in The Cancer Genome Atlas (TCGA) dataset were stratified according to the CRS signature enrichment score, and mutational profile and proportions of infiltrated immune cells were compared. Results In the discovery dataset (GSE53781), 95 genes were upregulated in complete responders compared to non‐complete responders and defined as the CRS signature. Pathways regarding DNA replication and repair processes as well as inflammatory response were enriched in the CRS signature. In the validation datasets (GSE35452 and GSE45404), patients with favorable response to nCRT exhibited higher enrichment score of the CRS. In TCGA‐READ cohort, patients with high CRS signature harbored KRAS mutation in lower frequency than those with low CRS signature. In addition, proportions of proinflammatory immune cells were higher, but proportion of immunosuppressive M2 macrophages was lower in patients with high CRS signature than those with low CRS signature. Conclusions The current integrative bioinformatic analysis suggests the CRS signature and showed that the CRS signature is associated with dissimilar mutational profile and increased immune response. The discovered CRS signature and related characteristics may serve as candidate of stratification factor in upcoming studies for rectal cancer.
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spelling doaj.art-dbdd210f023347f6a579ba0b4d43706a2023-04-27T10:12:44ZengWileyCancer Medicine2045-76342023-04-011278981899010.1002/cam4.5586Characterization of the gene signature correlated with favorable response to chemoradiotherapy in rectal cancer: A hypothesis‐generating studySeung Hyuck Jeon0Eui Kyu Chie1Graduate School of Medical Science and Engineering Korea Advanced Institute of Science and Technology Daejeon KoreaDepartment of Radiation Oncology Seoul National University College of Medicine Seoul KoreaAbstract Purpose This study aimed to define the gene signature associated with response to neoadjuvant chemoradiotherapy (nCRT), or chemoradiosensitivity (CRS) signature, in rectal cancer, and investigate the correlation between the CRS signature and characteristics of tumor. Materials and Methods Three public microarray datasets of pre‐nCRT rectal cancer were used to discover and validate the CRS signature, and the pathway analysis of the CRS signature was performed. Patients in The Cancer Genome Atlas (TCGA) dataset were stratified according to the CRS signature enrichment score, and mutational profile and proportions of infiltrated immune cells were compared. Results In the discovery dataset (GSE53781), 95 genes were upregulated in complete responders compared to non‐complete responders and defined as the CRS signature. Pathways regarding DNA replication and repair processes as well as inflammatory response were enriched in the CRS signature. In the validation datasets (GSE35452 and GSE45404), patients with favorable response to nCRT exhibited higher enrichment score of the CRS. In TCGA‐READ cohort, patients with high CRS signature harbored KRAS mutation in lower frequency than those with low CRS signature. In addition, proportions of proinflammatory immune cells were higher, but proportion of immunosuppressive M2 macrophages was lower in patients with high CRS signature than those with low CRS signature. Conclusions The current integrative bioinformatic analysis suggests the CRS signature and showed that the CRS signature is associated with dissimilar mutational profile and increased immune response. The discovered CRS signature and related characteristics may serve as candidate of stratification factor in upcoming studies for rectal cancer.https://doi.org/10.1002/cam4.5586gene signatureimmune cellneoadjuvant chemoradiotherapyrectal cancerresponse
spellingShingle Seung Hyuck Jeon
Eui Kyu Chie
Characterization of the gene signature correlated with favorable response to chemoradiotherapy in rectal cancer: A hypothesis‐generating study
Cancer Medicine
gene signature
immune cell
neoadjuvant chemoradiotherapy
rectal cancer
response
title Characterization of the gene signature correlated with favorable response to chemoradiotherapy in rectal cancer: A hypothesis‐generating study
title_full Characterization of the gene signature correlated with favorable response to chemoradiotherapy in rectal cancer: A hypothesis‐generating study
title_fullStr Characterization of the gene signature correlated with favorable response to chemoradiotherapy in rectal cancer: A hypothesis‐generating study
title_full_unstemmed Characterization of the gene signature correlated with favorable response to chemoradiotherapy in rectal cancer: A hypothesis‐generating study
title_short Characterization of the gene signature correlated with favorable response to chemoradiotherapy in rectal cancer: A hypothesis‐generating study
title_sort characterization of the gene signature correlated with favorable response to chemoradiotherapy in rectal cancer a hypothesis generating study
topic gene signature
immune cell
neoadjuvant chemoradiotherapy
rectal cancer
response
url https://doi.org/10.1002/cam4.5586
work_keys_str_mv AT seunghyuckjeon characterizationofthegenesignaturecorrelatedwithfavorableresponsetochemoradiotherapyinrectalcancerahypothesisgeneratingstudy
AT euikyuchie characterizationofthegenesignaturecorrelatedwithfavorableresponsetochemoradiotherapyinrectalcancerahypothesisgeneratingstudy