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A framework to predict the molecular classification and prognosis of breast cancer patients and characterize the landscape of immune cell infiltration

A framework to predict the molecular classification and prognosis of breast cancer patients and characterize the landscape of immune cell infiltration
A framework to predict the molecular classification and prognosis of breast cancer patients and characterize the landscape of immune cell infiltration
It is known that all current cancer therapies can only benefit a limited proportion of patients; thus, molecular classification and prognosis evaluation are critical for correctly classifying breast cancer patients and selecting the best treatment strategy. These processes usually involve the disclosure of molecular information like mutation, expression, and immune microenvironment of a breast cancer patient, which are not been fully studied until now. Therefore, there is an urgent clinical need to identify potential markers to enhance molecular classification, precision prognosis, and therapy stratification for breast cancer patients. In this study, we explored the gene expression profiles of 1,721 breast cancer patients through CIBERSORT and ESTIMATE algorithms; then, we obtained a comprehensive intratumoral immune landscape. The immune cell infiltration (ICI) patterns of breast cancer were classified into 3 separate subtypes according to the infiltration levels of 22 immune cells. The differentially expressed genes between these subtypes were further identified, and ICI scores were calculated to assess the immune landscape of BRCA patients. Importantly, we demonstrated that ICI scores correlate with patients’ survival, tumor mutation burden, neoantigens, and sensitivity to specific drugs. Based on these ICI scores, we were able to predict the prognosis of patients and their response to immunotherapy. Together, these findings provide a realistic scenario to stratify breast cancer patients for precision medicine.
Biomarkers, Tumor/genetics, Breast Neoplasms/genetics, Female, Gene Expression Regulation, Neoplastic, Humans, Mutation, Precision Medicine, Prognosis, Tumor Microenvironment/genetics
1748-670X
Zheng, Kun
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Luo, Zhiyong
3da5fc3a-70b1-45cc-bf1e-2ee6dd1f6ce1
Zhou, Yilu
1878565d-39e6-467d-a027-7320bf4cdaf2
Zhang, Lili
b69fc74a-a857-4181-98a0-1f691a9bec9c
Wang, Yali
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Chen, Xiuqiong
089a6c81-e1a2-4551-87cb-d848afb3bf5d
Yao, Shuo
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Xiong, Huihua
ea351243-345d-43ed-b55c-ebbad64669f0
Yuan, Xianglin
fa1f20ae-d03a-43dc-b13f-b826e665750d
Zou, Yanmei
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Wang, Yihua
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Xiong, Hua
d7236d3f-1ddb-4527-bc46-26b9571fcc17
Zheng, Kun
8ad20b1c-27e0-4048-9601-7ec2218fba7f
Luo, Zhiyong
3da5fc3a-70b1-45cc-bf1e-2ee6dd1f6ce1
Zhou, Yilu
1878565d-39e6-467d-a027-7320bf4cdaf2
Zhang, Lili
b69fc74a-a857-4181-98a0-1f691a9bec9c
Wang, Yali
1897d60f-dda5-46fa-b756-ed22e0712bfd
Chen, Xiuqiong
089a6c81-e1a2-4551-87cb-d848afb3bf5d
Yao, Shuo
102773aa-09c6-4097-a7e5-9636e2ea2801
Xiong, Huihua
ea351243-345d-43ed-b55c-ebbad64669f0
Yuan, Xianglin
fa1f20ae-d03a-43dc-b13f-b826e665750d
Zou, Yanmei
3917131c-49f0-4164-9e3a-ca27b0ef587e
Wang, Yihua
f5044a95-60a7-42d2-87d6-5f1f789e3a7e
Xiong, Hua
d7236d3f-1ddb-4527-bc46-26b9571fcc17

Zheng, Kun, Luo, Zhiyong, Zhou, Yilu, Zhang, Lili, Wang, Yali, Chen, Xiuqiong, Yao, Shuo, Xiong, Huihua, Yuan, Xianglin, Zou, Yanmei, Wang, Yihua and Xiong, Hua (2022) A framework to predict the molecular classification and prognosis of breast cancer patients and characterize the landscape of immune cell infiltration. Computational and Mathematical Methods in Medicine, 2022, [4635806]. (doi:10.1155/2022/4635806).

Record type: Article

Abstract

It is known that all current cancer therapies can only benefit a limited proportion of patients; thus, molecular classification and prognosis evaluation are critical for correctly classifying breast cancer patients and selecting the best treatment strategy. These processes usually involve the disclosure of molecular information like mutation, expression, and immune microenvironment of a breast cancer patient, which are not been fully studied until now. Therefore, there is an urgent clinical need to identify potential markers to enhance molecular classification, precision prognosis, and therapy stratification for breast cancer patients. In this study, we explored the gene expression profiles of 1,721 breast cancer patients through CIBERSORT and ESTIMATE algorithms; then, we obtained a comprehensive intratumoral immune landscape. The immune cell infiltration (ICI) patterns of breast cancer were classified into 3 separate subtypes according to the infiltration levels of 22 immune cells. The differentially expressed genes between these subtypes were further identified, and ICI scores were calculated to assess the immune landscape of BRCA patients. Importantly, we demonstrated that ICI scores correlate with patients’ survival, tumor mutation burden, neoantigens, and sensitivity to specific drugs. Based on these ICI scores, we were able to predict the prognosis of patients and their response to immunotherapy. Together, these findings provide a realistic scenario to stratify breast cancer patients for precision medicine.

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More information

Accepted/In Press date: 16 May 2022
e-pub ahead of print date: 7 June 2022
Published date: 7 June 2022
Additional Information: Copyright © 2022 Kun Zheng et al.
Keywords: Biomarkers, Tumor/genetics, Breast Neoplasms/genetics, Female, Gene Expression Regulation, Neoplastic, Humans, Mutation, Precision Medicine, Prognosis, Tumor Microenvironment/genetics

Identifiers

Local EPrints ID: 457832
URI: http://eprints.soton.ac.uk/id/eprint/457832
ISSN: 1748-670X
PURE UUID: d4bdfc91-6254-4d35-8f8d-7f63fc73911d
ORCID for Yilu Zhou: ORCID iD orcid.org/0000-0002-4090-099X
ORCID for Yihua Wang: ORCID iD orcid.org/0000-0001-5561-0648

Catalogue record

Date deposited: 20 Jun 2022 16:40
Last modified: 17 Mar 2024 03:39

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Contributors

Author: Kun Zheng
Author: Zhiyong Luo
Author: Yilu Zhou ORCID iD
Author: Lili Zhang
Author: Yali Wang
Author: Xiuqiong Chen
Author: Shuo Yao
Author: Huihua Xiong
Author: Xianglin Yuan
Author: Yanmei Zou
Author: Yihua Wang ORCID iD
Author: Hua Xiong

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