Protein Arginine Methylation: An Emerging Modification in Cancer Immunity and Immunotherapy

被引:23
作者
Dai, Weijing [1 ,2 ]
Zhang, Jianguo [1 ,2 ]
Li, Siqi [1 ,2 ]
He, Fajian [1 ,2 ]
Liu, Qiao [1 ,2 ]
Gong, Jun [1 ,2 ,3 ]
Yang, Zetian [4 ]
Gong, Yan [5 ,6 ]
Tang, Fang [1 ,2 ,3 ]
Wang, Zhihao [1 ,2 ,3 ]
Xie, Conghua [1 ,2 ,3 ]
机构
[1] Wuhan Univ, Dept Radiat & Med Oncol, Zhongnan Hosp, Wuhan, Peoples R China
[2] Wuhan Univ, Hubei Key Lab Tumor Biol Behav, Zhongnan Hosp, Wuhan, Peoples R China
[3] Wuhan Univ, Hubei Canc Clin Study Ctr, Zhongnan Hosp, Wuhan, Peoples R China
[4] Wuhan Univ, Dept Thorac Surg, Zhongnan Hosp, Wuhan, Peoples R China
[5] Wuhan Univ, Dept Biol Repositories, Zhongnan Hosp, Wuhan, Peoples R China
[6] Wuhan Univ, Hubei Engn Res Ctr, Tumor Precis Diag & Treatment Technol & Translat M, Zhongnan Hosp, Wuhan, Peoples R China
来源
FRONTIERS IN IMMUNOLOGY | 2022年 / 13卷
基金
中国国家自然科学基金;
关键词
protein arginine methyltransferases (PRMTs); cancer immunity; cancer immunotherapy; post translational; modification; molecular mechanism; TERTIARY LYMPHOID STRUCTURES; MHC CLASS-I; TUMOR-INFILTRATING LYMPHOCYTES; REGULATORY T-CELLS; METHYLTRANSFERASE; 5; IFN-GAMMA; ANTITUMOR IMMUNITY; GENE-EXPRESSION; C-MYC; ALTERNATIVE ACTIVATION;
D O I
10.3389/fimmu.2022.865964
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
In recent years, protein arginine methyltransferases (PRMTs) have emerged as new members of a gene expression regulator family in eukaryotes, and are associated with cancer pathogenesis and progression. Cancer immunotherapy has significantly improved cancer treatment in terms of overall survival and quality of life. Protein arginine methylation is an epigenetic modification function not only in transcription, RNA processing, and signal transduction cascades, but also in many cancer-immunity cycle processes. Arginine methylation is involved in the activation of anti-cancer immunity and the regulation of immunotherapy efficacy. In this review, we summarize the most up-to-date information on regulatory molecular mechanisms and different underlying arginine methylation signaling pathways in innate and adaptive immune responses during cancer. We also outline the potential of PRMT-inhibitors as effective combinatorial treatments with immunotherapy.
引用
收藏
页数:21
相关论文
共 205 条
[1]   A protein-arginine methyltransferase binds to the intracytoplasmic domain of the IFNAR1 chain in the type I interferon receptor [J].
Abramovich, C ;
Yakobson, B ;
Chebath, J ;
Revel, M .
EMBO JOURNAL, 1997, 16 (02) :260-266
[2]   CD28-mediated co-stimulation: A quantitative support for TCR signalling [J].
Acuto, O ;
Michel, F .
NATURE REVIEWS IMMUNOLOGY, 2003, 3 (12) :939-951
[3]   Protein Arginine Methyltransferase 5 Regulates ERK1/2 Signal Transduction Amplitude and Cell Fate Through CRAF [J].
Andreu-Perez, Pedro ;
Esteve-Puig, Rosaura ;
de Torre-Minguela, Carlos ;
Lopez-Fauqued, Marta ;
Josep Bech-Serra, Joan ;
Tenbaum, Stephan ;
Garcia-Trevijano, Elena R. ;
Canals, Francesc ;
Merlino, Glenn ;
Avila, Matias A. ;
Recio, Juan A. .
SCIENCE SIGNALING, 2011, 4 (190)
[4]   Dabrafenib, trametinib and pembrolizumab or placebo in BRAF-mutant melanoma [J].
Ascierto, Paolo Antonio ;
Ferrucci, Pier Francesco ;
Fisher, Rosalie ;
Del Vecchio, Michele ;
Atkinson, Victoria ;
Schmidt, Henrik ;
Schachter, Jacob ;
Queirolo, Paola ;
Long, Georgina V. ;
Di Giacomo, Anna Maria ;
Svane, Inge Marie ;
Lotem, Michal ;
Bar-Sela, Gil ;
Couture, Felix ;
Mookerjee, Bijoyesh ;
Ghori, Razi ;
Ibrahim, Nageatte ;
Moreno, Blanca Homet ;
Ribas, Antoni .
NATURE MEDICINE, 2019, 25 (06) :941-+
[5]   PRMT6 Promotes Lung Tumor Progression via the Alternate Activation of Tumor-Associated Macrophages [J].
Avasarala, Sreedevi ;
Wu, Pei-Ying ;
Khan, Samia Q. ;
Su Yanlin ;
Van Scoyk, Michelle ;
Bao, Jianqiang ;
Di Lorenzo, Alessandra ;
David, Odile ;
Bedford, Mark T. ;
Gupta, Vineet ;
Winn, Robert A. ;
Bikkavilli, Rama Kamesh .
MOLECULAR CANCER RESEARCH, 2020, 18 (01) :166-178
[6]   SPECIFIC ENZYMIC METHYLATION OF AN ARGININE IN EXPERIMENTAL ALLERGIC ENCEPHALOMYELITIS PROTEIN FROM HUMAN MYELIN [J].
BALDWIN, GS ;
CARNEGIE, PR .
SCIENCE, 1971, 171 (3971) :579-&
[7]   The tumor microenvironment at a glance [J].
Balkwill, Frances R. ;
Capasso, Melania ;
Hagemann, Thorsten .
JOURNAL OF CELL SCIENCE, 2012, 125 (23) :5591-5596
[8]   PRMT5-PTEN molecular pathway regulates senescence and self-renewal of primary glioblastoma neurosphere cells [J].
Banasavadi-Siddegowda, Y. K. ;
Russell, L. ;
Frair, E. ;
Karkhanis, V. A. ;
Relation, T. ;
Yoo, J. Y. ;
Zhang, J. ;
Sif, S. ;
Imitola, J. ;
Baiocchi, R. ;
Kaur, B. .
ONCOGENE, 2017, 36 (02) :263-274
[9]   Dynamic Treg interactions with intratumoral APCs promote local CTL dysfunction [J].
Bauer, Christian A. ;
Kim, Edward Y. ;
Marangoni, Francesco ;
Carrizosa, Esteban ;
Claudio, Natalie M. ;
Mempel, Thorsten R. .
JOURNAL OF CLINICAL INVESTIGATION, 2014, 124 (06) :2425-2440
[10]   Protein Arginine Methylation in Mammals: Who, What, and Why [J].
Bedford, Mark T. ;
Clarke, Steven G. .
MOLECULAR CELL, 2009, 33 (01) :1-13