This article is a correction to:
Antigen Presentation Machinery Signature-Derived CALR Mediates Migration, Polarization of Macrophages in Glioma and Predicts Immunotherapy Response
Rui Chen1†
Hao Zhang2,3†
Wantao Wu3,4†
Shuyu Li5†
Zeyu Wang2,3
Ziyu Dai2,3
Zaoqu Liu6
Jian Zhang7
Peng Luo7
Zhiwei Xia8*
Quan Cheng2,3*- 1Department of Neurosurgery, Affiliated Nanhua Hospital, University of South China, Hengyang, China
- 2Department of Neurosurgery, Xiangya Hospital, Central South University, Changsha, China
- 3National Clinical Research Center for Geriatric Disorders, Xiangya Hospital, Central South University, Changsha, China
- 4Department of Oncology, Xiangya Hospital, Central South University, Changsha, China
- 5Department of Thyroid and Breast Surgery, Tongji Hospital, Tongji Medical College of Huazhong University of Science and Technology, Wuhan, China
- 6Department of Interventional Radiology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China
- 7Department of Oncology, Zhujiang Hospital, Southern Medical University, Guangzhou, China
- 8Department of Neurology, Hunan Aerospace Hospital, Changsha, China
In the original article, there was a mistake in Figure 4G as published. The title of Figure 4G was mistakenly copyedited from the title of Figure 4F during the figure preparation. The corrected Figure 4 appears below.
FIGURE 4
Figure 4 Construction of APM signature gene-based risk score. (A) LASSO regression analysis showing the coefficients of APM signature genes. (B) Partial likelihood deviance of APM signature genes. (C) Bubble plot depicting the APM-derived risk signature genes. (D) Heatmap depicting the association between APM signature genes and risk score in the TCGA. (E) Heatmap depicting the association between APM signature genes and risk score in the CGGA. (F) The correlation between APM signature and risk score in TCGA. (G) The correlation between APM signature and risk score in the CGGA.
The authors apologize for this error and state that this does not change the scientific conclusions of the article in any way. The original article has been updated.
In the original article, there was a mistake in Figure 9E as published. Images (siRNA-CALR-1 group) were mistakenly chosen from the group named siRNA-NC during the figure preparation. The corrected Figure 9 appears below.
FIGURE 9
Figure 9 (A) Western blotting results for U251 cells treated with siRNAs. Statistical analysis of the western blotting results in different siRNA groups. (B) Statistical analysis of the qPCR results in different siRNA groups. (C) Diagram for the coculture between HMC3 and U251 cells. (D) Transwell assay for the cocultured HMC3 cells. Statistical analysis of the migrated HMC3 cells in different siRNA groups. (E) Immunofluorescence staining of CD68 and CD11c in HMC3 cells. (F) Immunofluorescence staining of CD68 and CD163 in HMC3 cells. *P < 0.05; **P < 0.01; ***P < 0.001; ****P < 0.0001.
The authors apologize for this error and state that this does not change the scientific conclusions of the article in any way. The original article has been updated.
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Keywords: antigen presentation machinery, glioma, microenvironment, prognosis, genomic alteration, immunotherapy
Citation: Chen R, Zhang H, Wu W, Li S, Wang Z, Dai Z, Liu Z, Zhang J, Luo P, Xia Z and Cheng Q (2022) Corrigendum: Antigen Presentation Machinery Signature-Derived CALR Mediates Migration, Polarization of Macrophages in Glioma and Predicts Immunotherapy Response. Front. Immunol. 13:931433. doi: 10.3389/fimmu.2022.931433
Received: 29 April 2022; Accepted: 13 May 2022;
Published: 02 June 2022.
Edited and reviewed by:
Fuming Qiu, Zhejiang University, ChinaCopyright © 2022 Chen, Zhang, Wu, Li, Wang, Dai, Liu, Zhang, Luo, Xia and Cheng. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Zhiwei Xia, eGlhemhpd2VpMjAxMUBnbWFpbC5jb20=; Quan Cheng, Y2hlbmdxdWFuQGNzdS5lZHUuY24=
†These authors have contributed equally to this work and share first authorship