Study of immunosenescence in the occurrence and immunotherapy of gastrointestinal malignancies

被引:0
|
作者
Dong, Daosong [1 ]
Yu, Xue [2 ]
Liu, Haoran [3 ]
Xu, Jingjing [4 ]
Guo, Jiayan [5 ]
Guo, Wei [6 ]
Li, Xiang [6 ]
Wang, Fei [7 ]
Zhang, Dongyong [8 ]
Liu, Kaiwei [9 ,10 ]
Sun, Yanbin [10 ]
机构
[1] China Med Univ, Hosp 1, Dept Pain, Shenyang 110001, Liaoning, Peoples R China
[2] China Med Univ, Hosp 1, Dept Surg Oncol & Gen Surg, Key Lab Mol Pathol & Epidemiol Gastr Canc Univ Lia, Shenyang 110001, Liaoning, Peoples R China
[3] China Med Univ, Hosp 1, Dept Breast Surg, Shenyang 110001, Peoples R China
[4] China Med Univ, Shengjing Hosp, Dept Rheumatol & Immunol, Shenyang 110001, Liaoning, Peoples R China
[5] China Med Univ, Hosp 1, Dept Plast Surg, Shenyang 110001, Peoples R China
[6] First Hosp China Med Univ, Dept Pancreat Biliary Surg, Shenyang 110001, Peoples R China
[7] China Med Univ, Hosp 1, Dept Otolaryngol, Shenyang 110001, Peoples R China
[8] China Med Univ, Hosp 1, Dept Neurosurg, Shenyang 110001, Peoples R China
[9] China Med Univ, Shengjing Hosp, Dept Ultrasound, Shenyang, Peoples R China
[10] First Hosp China Med Univ, Dept Geratol, Shenyang 110001, Peoples R China
关键词
Immunotherapy; Programmed death ligand-1 (PD-1) inhibitors; Cancer vaccines; Checkpoint inhibitors; Advanced gastric cancer; GASTROESOPHAGEAL JUNCTION CANCER; IMMUNE CHECKPOINT INHIBITORS; TUMOR-ASSOCIATED MACROPHAGES; T-LYMPHOCYTE ANTIGEN-4; NECROSIS-FACTOR-ALPHA; NATURAL-KILLER-CELLS; GASTRIC-CANCER; OPEN-LABEL; SINGLE-ARM; INDOLEAMINE 2,3-DIOXYGENASE;
D O I
10.1016/j.semcancer.2025.01.007
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
In human beings heterogenous, pervasive and lethal malignancies of different parts of the gastrointestinal (GI) tract viz., tumours of the oesophagus, stomach, small intestine, colon, and rectum, represent gastrointestinal malignancies. Primary treatment modality for gastric cancer includes chemotherapy, surgical interventions, radiotherapy, monoclonal antibodies and inhibitors of angiogenesis. However, there is a need to improve upon the existing treatment modality due to associated adverse events and the development of resistance towards treatment. Additionally, age has been found to contribute to increasing the incidence of tumours due to immunosenescence-associated immunosuppression. Immunosenescence is the natural process of ageing, wherein immune cells as well as organs begin to deteriorate resulting in a dysfunctional or malfunctioning immune system. Accretion of senescent cells in immunosenescence results in the creation of a persistent inflammatory environment or inflammaging, marked with elevated expression of pro-inflammatory and immunosuppressive cytokines and chemokines. Perturbation in the T-cell pools and persistent stimulation by the antigens facilitate premature senility of the immune cells, and senile immune cells exacerbate inflammaging conditions and the inefficiency of the immune system to identify the tumour antigen. Collectively, these conditions contribute positively towards tumour generation, growth and eventually proliferation. Thus, activating the immune cells to distinguish the tumour cells from normal cells and invade them seems to be a logical strategy for the treatment of cancer. Consequently, various approaches to immunotherapy, viz., programmed death ligand-1 (PD-1) inhibitors, Cytotoxic T-lymphocyte-associated protein 4 (CTLA-4) inhibitors etc are being extensively evaluated for their efficiency in gastric cancer. In fact, PD-1 inhibitors have been sanctioned as late late-line therapy modality for gastric cancer. The present review will focus on deciphering the link between the immune system and gastric cancer, and the alterations in the immune system that incur during the development of gastrointestinal malignancies. Also, the mechanism of evasion by tumour cells and immune checkpoints involved along with different approaches of immunotherapy being evaluated in different clinical trials will be discussed.
引用
收藏
页码:16 / 35
页数:20
相关论文
共 50 条
  • [1] Immunotherapy for Gastrointestinal Malignancies
    Toomey, Paul G.
    Vohra, Nasreen A.
    Ghansah, Tomar
    Sarnaik, Amod A.
    Pilon-Thomas, Shari A.
    CANCER CONTROL, 2013, 20 (01) : 32 - 42
  • [2] Immunotherapy in Gastrointestinal Malignancies
    Mizrahi, Jonathan
    Pant, Shubham
    IMMUNOTHERAPY, 3RD EDITION, 2020, 1244 : 93 - 106
  • [3] Immunotherapy in Gastrointestinal Malignancies
    Surana, Rishi
    Pant, Shubham
    IMMUNOTHERAPY, 4TH EDITION, 2021, 1342 : 259 - 272
  • [4] Immunotherapy—another breakthrough in gastrointestinal malignancies
    Monika Lenzi
    Thomas Winder
    memo - Magazine of European Medical Oncology, 2022, 15 : 20 - 25
  • [5] The coming of age: immunotherapy in gastrointestinal malignancies
    Mahalingam, Devalingam
    JOURNAL OF GASTROINTESTINAL ONCOLOGY, 2018, 9 (01) : 140 - 142
  • [6] Current immunotherapy in gastrointestinal malignancies A Review
    Dahiya, Dushyant Singh
    Kichloo, Asim
    Singh, Jagmeet
    Albosta, Michael
    Lekkala, Manidhar
    JOURNAL OF INVESTIGATIVE MEDICINE, 2021, 69 (03) : 689 - 696
  • [7] Current status of immunotherapy in gastrointestinal malignancies
    Lorenzen, Sylvie
    Lordick, Florian
    Loosen, Sven Heiko
    Tacke, Frank
    Trautwein, Christian
    Roderburg, Christoph
    Ettrich, Thomas J.
    Perkhofer, Lukas
    Reinacher-Schick, Anke
    Stein, Alexander
    ZEITSCHRIFT FUR GASTROENTEROLOGIE, 2020, 58 (06): : 542 - 555
  • [8] Immunotherapy in Melanoma, Gastrointestinal (GI), and Pulmonary Malignancies
    Dillon, Alexander B.
    Lin, Kevin
    Kwong, Andrew
    Ortiz, Susana
    AIMS PUBLIC HEALTH, 2015, 2 (01): : 86 - 114
  • [9] Immunotherapy-another breakthrough in gastrointestinal malignancies
    Lenzi, Monika
    Winder, Thomas
    MEMO-MAGAZINE OF EUROPEAN MEDICAL ONCOLOGY, 2022, 15 (01) : 20 - 25
  • [10] Current approaches to immunotherapy in noncolorectal gastrointestinal malignancies
    Fonseca de Jesus, Victor Hugo
    Felismino, Tiago Cordeiro
    de Barros e Silva, Milton Jose
    e Silva, Virgilio de Souza
    Riechelmann, Rachel P.
    CLINICS, 2018, 73