Literature DB >> 32679050

The role of genetic polymorphism within PD-L1 gene in cancer. Review.

Agnieszka Kula1, Miriam Dawidowicz2, Paweł Kiczmer2, Alicja Prawdzic Seńkowska2, Elżbieta Świętochowska2.   

Abstract

The maintenance of homeostasis of the immune system depends on the balance between excitatory and inhibitory signals. Programmed death ligand (PD-L1) is a molecule which downregulates the immune system targeting the programmed death receptor 1 (PD-1). Under physiological conditions, the receptor is constitutively expressed in lymphocytes. The PD-L1 / PD-1 pathway plays a key role in completing the immune response in the right way, preventing excessive stimulation of the cells of the immune system, protecting the organism against autoimmunity. Under pathological conditions PD-L1 expression may take place in tumor cells. Binding of PD-1 to its ligand on tumor cells suppresses T lymphocytes through a negative feedback. This mechanism allows abnormal cells to avoid destruction by the host immune system. The expression of PD-L1 in tumors has been described in many histological types of cancer: melanoma, lung cancer, breast and ovarian, pancreatic and esophagus adenocarcinoma, kidney tumors and bladder cancers as well as in hematopoietic malignancies. Many studies report a significant effect of PD-L1 polymorphisms on clinical parameters of patients. Studies of PD-L1 polymorphisms showed their influence on the stage of cancer, effectiveness of chemotherapy and prognosis after tumor resection. Further analysis of the polymorphisms may result in development of effective therapies that restore anti-tumor immunity. Inhibition of PD-L1 / PD-1 is one of the most promising immunotherapies for various types of cancer. This work was intended to present information about the impact of PD-L1 gene expression and polymorphisms on the clinical parameters of patients with cancer.
Copyright © 2020 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Cancer; Immunology; Programmed death ligand 1(PD-L1); Single nucleotide polymorphism (SNP)

Mesh:

Substances:

Year:  2020        PMID: 32679050     DOI: 10.1016/j.yexmp.2020.104494

Source DB:  PubMed          Journal:  Exp Mol Pathol        ISSN: 0014-4800            Impact factor:   3.362


  4 in total

1.  Prognostic Function of Programmed Cell Death-Ligand 1 in Esophageal Squamous Cell Carcinoma Patients Without Preoperative Therapy: A Systematic Review and Meta-Analysis.

Authors:  Hongxia Cui; Yarong Li; Su Li; Guangxuan Liu
Journal:  Front Oncol       Date:  2021-08-18       Impact factor: 6.244

2.  Prognostic value of immune factors in the tumor microenvironment of patients with pancreatic ductal adenocarcinoma.

Authors:  Sachie Kiryu; Zensho Ito; Machi Suka; Tsuuse Bito; Shin Kan; Kan Uchiyama; Masayuki Saruta; Taigo Hata; Yuki Takano; Shuichi Fujioka; Takeyuki Misawa; Takashi Yamauchi; Hiroyuki Yanagisawa; Nobuhiro Sato; Toshifumi Ohkusa; Haruo Sugiyama; Shigeo Koido
Journal:  BMC Cancer       Date:  2021-11-10       Impact factor: 4.430

Review 3.  Recent advances in primary resistance mechanisms against immune checkpoint inhibitors.

Authors:  Yi-Ze Li; Hong-Mei Zhang
Journal:  Curr Opin Oncol       Date:  2022-01-01       Impact factor: 3.645

4.  Assessing PD-L1 Expression Status Using Radiomic Features from Contrast-Enhanced Breast MRI in Breast Cancer Patients: Initial Results.

Authors:  Roberto Lo Gullo; Hannah Wen; Jeffrey S Reiner; Raza Hoda; Varadan Sevilimedu; Danny F Martinez; Sunitha B Thakur; Maxine S Jochelson; Peter Gibbs; Katja Pinker
Journal:  Cancers (Basel)       Date:  2021-12-14       Impact factor: 6.639

  4 in total

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