Association of CSMD1 with Tumor Mutation Burden and Other Clinical Outcomes in Gastric Cancer

Xuning Wang,1,2,* Shixiang Wang,3,* Yalin Han,1,4 Maolin Xu,1 Peng Li,1 Mu Ke,1 Zhipeng Teng,1 Pu Huang,1 Ziyan Diao,2,5 Yongfeng Yan,1 Qingyu Meng,1 Yanshen Kuang,1 Wei Zheng,1 Hongyi Liu,1 Xuesong Liu,3 Baoqing Jia1 1The Air Force Hospital of Northern Theater PLA, Shenyang, People’...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Wang X, Wang S, Han Y, Xu M, Li P, Ke M, Teng Z, Huang P, Diao Z, Yan Y, Meng Q, Kuang Y, Zheng W, Liu H, Liu X, Jia B
Formato: article
Lenguaje:EN
Publicado: Dove Medical Press 2021
Materias:
Acceso en línea:https://doaj.org/article/1af56eeb7b534e208fa176bad5a045fa
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:1af56eeb7b534e208fa176bad5a045fa
record_format dspace
spelling oai:doaj.org-article:1af56eeb7b534e208fa176bad5a045fa2021-11-16T18:47:50ZAssociation of CSMD1 with Tumor Mutation Burden and Other Clinical Outcomes in Gastric Cancer1178-7074https://doaj.org/article/1af56eeb7b534e208fa176bad5a045fa2021-11-01T00:00:00Zhttps://www.dovepress.com/association-of-csmd1-with-tumor-mutation-burden-and-other-clinical-out-peer-reviewed-fulltext-article-IJGMhttps://doaj.org/toc/1178-7074Xuning Wang,1,2,* Shixiang Wang,3,* Yalin Han,1,4 Maolin Xu,1 Peng Li,1 Mu Ke,1 Zhipeng Teng,1 Pu Huang,1 Ziyan Diao,2,5 Yongfeng Yan,1 Qingyu Meng,1 Yanshen Kuang,1 Wei Zheng,1 Hongyi Liu,1 Xuesong Liu,3 Baoqing Jia1 1The Air Force Hospital of Northern Theater PLA, Shenyang, People’s Republic of China; 2Department of General Surgery, The First Center of Chinese PLA General Hospital, Beijing, People’s Republic of China; 3School of Life Science and Technology, ShanghaiTech University, Shanghai, People’s Republic of China; 4PLA Rocket Force Characteristic Medical Center, Beijing, People’s Republic of China; 5Chinese PLA Medical School, Beijing, People’s Republic of China*These authors contributed equally to this workCorrespondence: Baoqing JiaDepartment of General Surgery, The First Center of Chinese PLA General Hospital, Beijing, People’s Republic of ChinaEmail baoqingjia@126.comXuesong LiuSchool of Life Science and Technology, ShanghaiTech University, Shanghai, People’s Republic of ChinaEmail liuxs@shanghaitech.edu.cnBackground: Immunotherapy is considered as a powerful and promising clinical approach for the treatment of gastric cancer (GC). However, it is still challenging to precisely screen patients who potentially benefit from immune checkpoint therapy (ICT). Identification of potential biomarkers for selecting patients sensitive to immunotherapy was urgently needed.Methods: Public sequence data and corresponding clinical data were used to explore the potential biomarkers for immunotherapy.Results: We found that CSMD1 is the most frequently mutated gene and its mutation is highly correlated with prognosis in gastric cancer patients. Interestingly, patients with mutated CSMD1 exhibit a high mutation burden and upregulated PDL1 expression. The ratio of microsatellite instability (MSI) in the CSMD1 mutation cohort was higher than that in the cohort without CSMD1 mutation. Furthermore, patients with CSMD1 mutation have been found to possess a higher number of activated CD4+ T cells and neoantigens.Conclusion: CSMD1 mutation may act as a novel biomarker for assessing the survival and immune therapy response in patients with gastric cancer.Keywords: CSMD1, PDL1, tumor mutation burden, gastric cancerWang XWang SHan YXu MLi PKe MTeng ZHuang PDiao ZYan YMeng QKuang YZheng WLiu HLiu XJia BDove Medical Pressarticlecsmd1pdl1tumor mutation burdengastric cancerMedicine (General)R5-920ENInternational Journal of General Medicine, Vol Volume 14, Pp 8293-8299 (2021)
institution DOAJ
collection DOAJ
language EN
topic csmd1
pdl1
tumor mutation burden
gastric cancer
Medicine (General)
R5-920
spellingShingle csmd1
pdl1
tumor mutation burden
gastric cancer
Medicine (General)
R5-920
Wang X
Wang S
Han Y
Xu M
Li P
Ke M
Teng Z
Huang P
Diao Z
Yan Y
Meng Q
Kuang Y
Zheng W
Liu H
Liu X
Jia B
Association of CSMD1 with Tumor Mutation Burden and Other Clinical Outcomes in Gastric Cancer
description Xuning Wang,1,2,* Shixiang Wang,3,* Yalin Han,1,4 Maolin Xu,1 Peng Li,1 Mu Ke,1 Zhipeng Teng,1 Pu Huang,1 Ziyan Diao,2,5 Yongfeng Yan,1 Qingyu Meng,1 Yanshen Kuang,1 Wei Zheng,1 Hongyi Liu,1 Xuesong Liu,3 Baoqing Jia1 1The Air Force Hospital of Northern Theater PLA, Shenyang, People’s Republic of China; 2Department of General Surgery, The First Center of Chinese PLA General Hospital, Beijing, People’s Republic of China; 3School of Life Science and Technology, ShanghaiTech University, Shanghai, People’s Republic of China; 4PLA Rocket Force Characteristic Medical Center, Beijing, People’s Republic of China; 5Chinese PLA Medical School, Beijing, People’s Republic of China*These authors contributed equally to this workCorrespondence: Baoqing JiaDepartment of General Surgery, The First Center of Chinese PLA General Hospital, Beijing, People’s Republic of ChinaEmail baoqingjia@126.comXuesong LiuSchool of Life Science and Technology, ShanghaiTech University, Shanghai, People’s Republic of ChinaEmail liuxs@shanghaitech.edu.cnBackground: Immunotherapy is considered as a powerful and promising clinical approach for the treatment of gastric cancer (GC). However, it is still challenging to precisely screen patients who potentially benefit from immune checkpoint therapy (ICT). Identification of potential biomarkers for selecting patients sensitive to immunotherapy was urgently needed.Methods: Public sequence data and corresponding clinical data were used to explore the potential biomarkers for immunotherapy.Results: We found that CSMD1 is the most frequently mutated gene and its mutation is highly correlated with prognosis in gastric cancer patients. Interestingly, patients with mutated CSMD1 exhibit a high mutation burden and upregulated PDL1 expression. The ratio of microsatellite instability (MSI) in the CSMD1 mutation cohort was higher than that in the cohort without CSMD1 mutation. Furthermore, patients with CSMD1 mutation have been found to possess a higher number of activated CD4+ T cells and neoantigens.Conclusion: CSMD1 mutation may act as a novel biomarker for assessing the survival and immune therapy response in patients with gastric cancer.Keywords: CSMD1, PDL1, tumor mutation burden, gastric cancer
format article
author Wang X
Wang S
Han Y
Xu M
Li P
Ke M
Teng Z
Huang P
Diao Z
Yan Y
Meng Q
Kuang Y
Zheng W
Liu H
Liu X
Jia B
author_facet Wang X
Wang S
Han Y
Xu M
Li P
Ke M
Teng Z
Huang P
Diao Z
Yan Y
Meng Q
Kuang Y
Zheng W
Liu H
Liu X
Jia B
author_sort Wang X
title Association of CSMD1 with Tumor Mutation Burden and Other Clinical Outcomes in Gastric Cancer
title_short Association of CSMD1 with Tumor Mutation Burden and Other Clinical Outcomes in Gastric Cancer
title_full Association of CSMD1 with Tumor Mutation Burden and Other Clinical Outcomes in Gastric Cancer
title_fullStr Association of CSMD1 with Tumor Mutation Burden and Other Clinical Outcomes in Gastric Cancer
title_full_unstemmed Association of CSMD1 with Tumor Mutation Burden and Other Clinical Outcomes in Gastric Cancer
title_sort association of csmd1 with tumor mutation burden and other clinical outcomes in gastric cancer
publisher Dove Medical Press
publishDate 2021
url https://doaj.org/article/1af56eeb7b534e208fa176bad5a045fa
work_keys_str_mv AT wangx associationofcsmd1withtumormutationburdenandotherclinicaloutcomesingastriccancer
AT wangs associationofcsmd1withtumormutationburdenandotherclinicaloutcomesingastriccancer
AT hany associationofcsmd1withtumormutationburdenandotherclinicaloutcomesingastriccancer
AT xum associationofcsmd1withtumormutationburdenandotherclinicaloutcomesingastriccancer
AT lip associationofcsmd1withtumormutationburdenandotherclinicaloutcomesingastriccancer
AT kem associationofcsmd1withtumormutationburdenandotherclinicaloutcomesingastriccancer
AT tengz associationofcsmd1withtumormutationburdenandotherclinicaloutcomesingastriccancer
AT huangp associationofcsmd1withtumormutationburdenandotherclinicaloutcomesingastriccancer
AT diaoz associationofcsmd1withtumormutationburdenandotherclinicaloutcomesingastriccancer
AT yany associationofcsmd1withtumormutationburdenandotherclinicaloutcomesingastriccancer
AT mengq associationofcsmd1withtumormutationburdenandotherclinicaloutcomesingastriccancer
AT kuangy associationofcsmd1withtumormutationburdenandotherclinicaloutcomesingastriccancer
AT zhengw associationofcsmd1withtumormutationburdenandotherclinicaloutcomesingastriccancer
AT liuh associationofcsmd1withtumormutationburdenandotherclinicaloutcomesingastriccancer
AT liux associationofcsmd1withtumormutationburdenandotherclinicaloutcomesingastriccancer
AT jiab associationofcsmd1withtumormutationburdenandotherclinicaloutcomesingastriccancer
_version_ 1718426222722023424