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pmid:33666342

Identification of hub genes associated with neutrophils infiltration in colorectal cancer.

Hao Su · Tianyi Cai · Sen Zhang · Xialin Yan · Leqi Zhou · Zirui He · Pei Xue · Jianwen Li · Minhua Zheng · Xiao Yang · Bo Feng

Journal of cellular and molecular medicine · 2021 doi:10.1111/jcmm.16414

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Experiment

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pmid:33666342
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2026-11-01T15:41:27Z
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title
Identification of hub genes associated with neutrophils infiltration in colorectal cancer.
doi
10.1111/jcmm.16414
pmid
33666342
authors array · 11 items
[0]
Hao Su
[1]
Tianyi Cai
[2]
Sen Zhang
[3]
Xialin Yan
[4]
Leqi Zhou
[5]
Zirui He
[6]
Pei Xue
[7]
Jianwen Li
[8]
Minhua Zheng
[9]
Xiao Yang
[10]
Bo Feng
journal
Journal of cellular and molecular medicine
year
2021
abstract
Colorectal cancer (CRC) is the leading cause of cancer-related mortality in the world. Accumulating evidence indicate that tumour infiltrating immune cells participated in cancer progression. Among them, tumour infiltrating neutrophils (TINs) are reported to play crucial role in various cancers. In this study, we used CIBERSORTx, a digital cytometry tool to evaluate the neutrophils infiltration in CRC based on gene expression data of CRC tissues from GSE39582 data set and The Cancer Genome Atlas data set (TCGA-COAD and TCGA-READ). Weighted gene co-expression network analysis (WGCNA) was conducted in GSE39582 data set to identify hub genes associated with neutrophil infiltration. The association of hub gene and neutrophils was then validated in TCGA cohorts and an independent RJ cohort. Functional analysis was performed to investigate the molecular mechanisms of the interested hub gene. We found that neutrophil infiltration is elevated in CRC tissues, and it is related to a poorer prognosis. A total of 18 gene modules are identified by WGCNA in GSE39582 data set, among which lightcyan module is significantly correlated with neutrophils infiltration. Furthermore, Superoxide Dismutase 2 (SOD2) in lightcyan module was proved to correlated with neutrophils infiltration in various cancer types. In addition, SOD2 expression is highly associated with several chemokines, including CXCL8, a neutrophils-related attractant, and functional analysis revealed that SOD2 is involved in neutrophils recruitment biological process. These results indicate that an 'SOD2-CXCL8-neutrophil recruitment' axis plays a potential role in colorectal cancer progression.
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Wilcoxon test was used to compare the neutrophil scores/counts in different sample groups.
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sections[9] "Statistics and data visualization" paragraph 2
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Wilcoxon test was used to compare the neutrophil scores/counts in different sample groups.
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The RNA sequencing data of CRC patients were downloaded from Xena (http://xena.ucsc.edu/). GSE39582 and GSE36133 were obtained from GEO database (https://www.ncbi.nlm.nih.gov/gds/). Other data analysed during this study are included in this published article and the supplementary material.
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sections[23] "DATA AVAILABILITY STATEMENT" paragraph 2
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The RNA sequencing data of CRC patients were downloaded from Xena (http://xena.ucsc.edu/). GSE39582 and GSE36133 were obtained from GEO database (https://www.ncbi.nlm.nih.gov/gds/). Other data analysed during this study are included in this published article and the supplementary material.
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https://doi.org/10.1111/jcmm.16414
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The RNA sequencing data of CRC patients were downloaded from Xena (http://xena.ucsc.edu/). GSE39582 and GSE36133 were obtained from GEO database (https://www.ncbi.nlm.nih.gov/gds/). Other data analysed during this study are included in this published article and the supplementary material.
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The RNA sequencing data of CRC patients were downloaded from Xena (http://xena.ucsc.edu/). GSE39582 and GSE36133 were obtained from GEO database (https://www.ncbi.nlm.nih.gov/gds/). Other data analysed during this study are included in this published article and the supplementary material.
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[498]
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[499]
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[500]
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[501]
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[502]
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[503]
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[504]
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[505]
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[506]
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[507]
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[508]
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[509]
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[510]
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[511]
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[512]
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[513]
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[514]
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[515]
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[516]
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[517]
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[518]
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[519]
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[520]
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[521]
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[522]
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[523]
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[524]
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[525]
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[526]
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[527]
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[528]
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[529]
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[530]
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[531]
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[532]
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[533]
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[534]
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[535]
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[536]
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[537]
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[538]
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[539]
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[540]
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[541]
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[542]
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[543]
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[544]
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[545]
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[546]
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[547]
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[548]
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[549]
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[550]
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[551]
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[552]
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[553]
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[554]
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[555]
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[556]
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[557]
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[558]
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[559]
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[560]
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[561]
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[562]
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[563]
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[564]
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[565]
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[566]
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[567]
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[568]
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[569]
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[570]
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[571]
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[572]
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[573]
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[574]
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[575]
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[576]
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[577]
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[578]
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[579]
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[580]
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[581]
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[582]
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[583]
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[584]
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[585]
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[586]
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[587]
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[588]
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[589]
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[590]
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[591]
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[592]
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[593]
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[594]
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[595]
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[596]
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[597]
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[598]
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[599]
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[600]
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[601]
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[602]
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[603]
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[604]
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[605]
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[606]
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[607]
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[608]
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[609]
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[610]
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[611]
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[612]
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[613]
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[614]
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[615]
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[616]
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[617]
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[618]
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[619]
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[620]
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[621]
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[622]
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[623]
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[624]
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[625]
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[626]
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[627]
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[628]
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[629]
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[630]
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[631]
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[632]
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[633]
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[634]
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[635]
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[636]
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[637]
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[638]
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[639]
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[640]
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[641]
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[642]
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[643]
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[644]
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[645]
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[646]
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[647]
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[648]
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[650]
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[652]
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[657]
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[662]
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[667]
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[668]
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[671]
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[675]
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[676]
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[677]
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[678]
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[679]
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[680]
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[685]
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[687]
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[688]
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[689]
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[690]
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[691]
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[692]
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[698]
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[699]
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[700]
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[701]
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[702]
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[703]
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[704]
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[705]
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[706]
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[707]
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[708]
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[709]
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[710]
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[711]
GSM887546
[712]
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[713]
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[714]
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[715]
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[716]
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[717]
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[718]
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[719]
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[721]
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[722]
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[723]
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[724]
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[726]
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[727]
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[729]
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[734]
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[735]
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[738]
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[741]
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[742]
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[743]
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[746]
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[747]
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[748]
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[749]
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[752]
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[759]
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[760]
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[761]
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[762]
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[763]
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[764]
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[765]
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[766]
GSM887601
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[768]
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[769]
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[770]
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[771]
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[772]
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[773]
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[774]
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[775]
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[776]
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[777]
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[778]
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[779]
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[780]
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[781]
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[782]
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[783]
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[784]
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[785]
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[786]
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[787]
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[789]
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[792]
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[793]
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[794]
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[797]
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[798]
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[799]
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[800]
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[801]
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[802]
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[803]
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[813]
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[814]
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[815]
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[818]
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[820]
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[821]
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[822]
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[823]
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[824]
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[825]
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[826]
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[827]
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[828]
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[829]
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GSM887740
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GSM887748
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GSM887749
[915]
GSM887750
[916]
GSM887751
sample_count
917
group_sizes
null
group_sizes_basis
null
platform
15308
taxon
Homo sapiens
title
Expression data from the Cancer Cell Line Encyclopedia (CCLE)
resolution_checked_at
2026-11-01T15:39:54Z
resolution_check
identifier_resolution_only_no_download_no_licence_read
downloaded
false
licence_read
false
[2] object · 15 fields
id
data:geo:GSE39582
role
raw
format
geo-series
media_type
application/vnd.ncbi.geo-series+json
uri
https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE39582
sha256
null
bytes
null
access
open
state
resolved
reader
null
reader_status
reader_required
identifier
GSE39582
version
null
note
The RNA sequencing data of CRC patients were downloaded from Xena (http://xena.ucsc.edu/). GSE39582 and GSE36133 were obtained from GEO database (https://www.ncbi.nlm.nih.gov/gds/). Other data analysed during this study are included in this published article and the supplementary material.
structure object · 15 fields
repository
GEO
access_route
GEO accession URL
access_statement_verbatim
The RNA sequencing data of CRC patients were downloaded from Xena (http://xena.ucsc.edu/). GSE39582 and GSE36133 were obtained from GEO database (https://www.ncbi.nlm.nih.gov/gds/). Other data analysed during this study are included in this published article and the supplementary material.
access_statement_kind
data_availability_statement
sample_accessions array · 585 items
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[6]
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[8]
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[20]
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[23]
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[24]
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[25]
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[26]
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[27]
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[28]
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[29]
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[30]
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[32]
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[34]
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[35]
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[37]
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[38]
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[39]
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[40]
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[41]
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[43]
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[44]
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[49]
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[70]
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[71]
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[73]
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[75]
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[78]
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title
Gene expression Classification of Colon Cancer defines six molecular subtypes with distinct clinical, molecular and survival characteristics [Expression]
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The RNA sequencing data of CRC patients were downloaded from Xena (http://xena.ucsc.edu/). GSE39582 and GSE36133 were obtained from GEO database (https://www.ncbi.nlm.nih.gov/gds/). Other data analysed during this study are included in this published article and the supplementary material.
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The paper names GSE39582, GSE36133 in Gene Expression Omnibus (GEO) and the accession resolves in the repository. No dataset was downloaded and no licence was read.
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oaded from Gene Expression Omnibus (GEO). 11 RNA sequencing data of 17 382 samples of 30 different types
[1]
m Xena (https://xenabrowser.net/datapages/). Transcriptome data of 566 colorectal cancer (CRC) samples
[2]
ype‐Tissue Expression (GTEx) project, 12 and transcriptome of 917 cancer cell line derived from tumour
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of RJ Cohort from our hospital were used for immunohistochemical validation. In RJ cohort, a total of 79 pati
[1]
ther validation. RJ cohort were utilized for immunohistochemistry Higher TIN levels indicating poorer prognosi
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:33666342", "kind": "science-record", "revision": 7, "content_hash": "sha256:d9c41d8350eef5d486f4614ebac17eca7e61ccdd7be01fa4f3379af134b88330", "created_at": "2026-11-01T15:41:27Z", "updated_at": "2026-11-01T22:03:14Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Identification of hub genes associated with neutrophils infiltration in colorectal cancer.", "doi": "10.1111/jcmm.16414", "pmid": "33666342", "authors": ["Hao Su", "Tianyi Cai", "Sen Zhang", "Xialin Yan", "Leqi Zhou", "Zirui He", "Pei Xue", "Jianwen Li", "Minhua Zheng", "Xiao Yang", "Bo Feng"], "journal": "Journal of cellular and molecular medicine", "year": 2021, "abstract": "Colorectal cancer (CRC) is the leading cause of cancer-related mortality in the world. Accumulating evidence indicate that tumour infiltrating immune cells participated in cancer progression. Among them, tumour infiltrating neutrophils (TINs) are reported to play crucial role in various cancers. In this study, we used CIBERSORTx, a digital cytometry tool to evaluate the neutrophils infiltration in CRC based on gene expression data of CRC tissues from GSE39582 data set and The Cancer Genome Atlas data set (TCGA-COAD and TCGA-READ). Weighted gene co-expression network analysis (WGCNA) was conducted in GSE39582 data set to identify hub genes associated with neutrophil infiltration. The association of hub gene and neutrophils was then validated in TCGA cohorts and an independent RJ cohort. Functional analysis was performed to investigate the molecular mechanisms of the interested hub gene. We found that neutrophil infiltration is elevated in CRC tissues, and it is related to a poorer prognosis. A total of 18 gene modules are identified by WGCNA in GSE39582 data set, among which lightcyan module is significantly correlated with neutrophils infiltration. Furthermore, Superoxide Dismutase 2 (SOD2) in lightcyan module was proved to correlated with neutrophils infiltration in various cancer types. In addition, SOD2 expression is highly associated with several chemokines, including CXCL8, a neutrophils-related attractant, and functional analysis revealed that SOD2 is involved in neutrophils recruitment biological process. 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