Immunosenescence and cancer: Opportunities and challenges

被引:11
作者
Fu, Zhibin [1 ]
Xu, Hailong [2 ]
Yue, Lanping [2 ]
Zheng, Weiwei [2 ]
Pan, Linkang [2 ]
Gao, Fangyi [2 ]
Liu, Xingshan [2 ]
机构
[1] Shandong Univ Tradit Chinese Med, Weifang Hosp Tradit Chinese Med, Weifang, Shandong, Peoples R China
[2] Weifang Hosp Tradit Chinese Med, Weifang 261000, Shandong, Peoples R China
关键词
aging; immunosenescence; senescence; tumor microenvironment; IMMUNE CHECKPOINT INHIBITORS; EXTENDS LIFE-SPAN; T-CELLS; REPLICATIVE SENESCENCE; IMMUNOLOGICAL THEORY; MELANOMA PATIENTS; AGE; RAPAMYCIN; ACTIVATION; REGULATOR;
D O I
10.1097/MD.0000000000036045
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
As individuals age, cancer becomes increasingly common. This continually rising risk can be attributed to various interconnected factors that influence the body's susceptibility to cancer. Among these factors, the accumulation of senescent cells in tissues and the subsequent decline in immune cell function and proliferative potential are collectively referred to as immunosenescence. Reduced T-cell production, changes in secretory phenotypes, increased glycolysis, and the generation of reactive oxygen species are characteristics of immunosenescence that contribute to cancer susceptibility. In the tumor microenvironment, senescent immune cells may promote the growth and spread of tumors through multiple pathways, thereby affecting the effectiveness of immunotherapy. In recent years, immunosenescence has gained increasing attention due to its critical role in tumor development. However, our understanding of how immunosenescence specifically impacts cancer immunotherapy remains limited, primarily due to the underrepresentation of elderly patients in clinical trials. Furthermore, there are several age-related intervention methods, including metformin and rapamycin, which involve genetic and pharmaceutical approaches. This article aims to elucidate the defining characteristics of immunosenescence and its impact on malignant tumors and immunotherapy. We particularly focus on the future directions of cancer treatment, exploring the complex interplay between immunosenescence, cancer, and potential interventions.
引用
收藏
页数:7
相关论文
共 117 条
[41]   Understanding immunosenescence to improve responses to vaccines [J].
Goronzy, Joerg J. ;
Weyand, Cornelia M. .
NATURE IMMUNOLOGY, 2013, 14 (05) :428-436
[42]   Mechanisms underlying T cell ageing [J].
Goronzy, Jorg J. ;
Weyand, Cornelia M. .
NATURE REVIEWS IMMUNOLOGY, 2019, 19 (09) :573-583
[43]   Successful and Maladaptive T Cell Aging [J].
Goronzy, Jorg J. ;
Weyand, Cornelia M. .
IMMUNITY, 2017, 46 (03) :364-378
[44]   A Diverse Array of Cancer-Associated MTOR Mutations Are Hyperactivating and Can Predict Rapamycin Sensitivity [J].
Grabiner, Brian C. ;
Nardi, Valentina ;
Birsoy, Kivan ;
Possemato, Richard ;
Shen, Kuang ;
Sinha, Sumi ;
Jordan, Alexander ;
Beck, Andrew H. ;
Sabatini, David M. .
CANCER DISCOVERY, 2014, 4 (05) :554-563
[45]   Age-related increase of tumor susceptibility is associated with myeloid-derived suppressor cell mediated suppression of T cell cytotoxicity in recombinant inbred BXD12 mice [J].
Grizzle, William E. ;
Xu, Xin ;
Zhang, Shuangqin ;
Stockard, Cecil R. ;
Liu, Cunren ;
Yu, Shaohua ;
Wang, Jianhua ;
Mountz, John D. ;
Zhang, Huang-Ge .
MECHANISMS OF AGEING AND DEVELOPMENT, 2007, 128 (11-12) :672-680
[46]   DCAF1 regulates Treg senescence via the ROS axis during immunological aging [J].
Guo, Zengli ;
Wang, Gang ;
Wu, Bing ;
Chou, Wei-Chun ;
Cheng, Liang ;
Zhou, Chenlin ;
Lou, Jitong ;
Wu, Di ;
Su, Lishan ;
Zheng, Junnian ;
Ting, Jenny P-Y ;
Wan, Yisong Y. .
JOURNAL OF CLINICAL INVESTIGATION, 2020, 130 (11) :5893-5908
[47]   Rapamycin increases rDNA stability by enhancing association of Sir2 with rDNA in Saccharomyces cerevisiae [J].
Ha, Cheol Woong ;
Huh, Won-Ki .
NUCLEIC ACIDS RESEARCH, 2011, 39 (04) :1336-1350
[48]   Thymic output in aged mice [J].
Hale, J. Scott ;
Boursalian, Tamar E. ;
Turk, Gail L. ;
Fink, Pamela J. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (22) :8447-8452
[49]   Rapamycin fed late in life extends lifespan in genetically heterogeneous mice [J].
Harrison, David E. ;
Strong, Randy ;
Sharp, Zelton Dave ;
Nelson, James F. ;
Astle, Clinton M. ;
Flurkey, Kevin ;
Nadon, Nancy L. ;
Wilkinson, J. Erby ;
Frenkel, Krystyna ;
Carter, Christy S. ;
Pahor, Marco ;
Javors, Martin A. ;
Fernandez, Elizabeth ;
Miller, Richard A. .
NATURE, 2009, 460 (7253) :392-U108
[50]   Loss of T cell receptor-induced Bmi-1 in the KLRG1+ senescent CD8+ T lymphocyte [J].
Heffner, Maike ;
Fearon, Douglas T. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2007, 104 (33) :13414-13419