Literature DB >> 28951311

PD-1 pathway and its clinical application: A 20year journey after discovery of the complete human PD-1 gene.

Kristin Nicole Berger1, Jeffrey Jiayu Pu2.   

Abstract

Anti-PD-1 therapy is a novel immune-checkpoint inhibition therapy with tremendous potential in treating refractory/relapsed cancers. The 20year journey of human PD-1 research went through 3 phases: 1) discovering PD-1 gene structure and genomic organization, 2) understanding the mechanism of PD-1 mediated immune-checkpoint regulatory effects in coordination with its ligands (PD-L1 and L2), 3) and translating our knowledge of PD-1 gene into a robust clinical anticancer approach by targeting the PD-1 immune-checkpoint pathway. The success of human PD-1 gene study reflects the advancement and trends of modern biomedical research from the laboratory to the bedside. However, our journey of understanding the PD-1 gene is not yet complete. Clinical investigation data show a high variety of response rates among different types of cancers to PD-1 immune-checkpoint inhibition therapy, with a range of 18% to 87%. There is no reliable biomarker to predict an individual patient's response to PD-1 inhibitory immunotherapy. Patients can present with primary, adaptive, or even acquired resistance to PD-1 immune-checkpoint inhibition therapy. Furthermore, the emerging data demonstrates that certain patients experience hyperprogressive disease status after receiving PD-1 immune-checkpoint inhibition therapy. In conclusion, PD-1 immune-checkpoint inhibition therapy has opened up a new venue of advanced cancer immunotherapy. Meanwhile, further efforts are still warranted in both basic scientific mechanism studies and clinical investigation using the principles of personalized and precision medicine.
Copyright © 2017 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Human Programmed Cell Death 1 (hPD-1) gene; Hyperprogressive disease status; Immune-checkpoint inhibition; Immunotherapy

Mesh:

Substances:

Year:  2017        PMID: 28951311     DOI: 10.1016/j.gene.2017.09.050

Source DB:  PubMed          Journal:  Gene        ISSN: 0378-1119            Impact factor:   3.688


  31 in total

1.  PD-L1 receptor expression in vulvar carcinomas is HPV-independent.

Authors:  M Choschzick; A Gut; D Fink
Journal:  Virchows Arch       Date:  2018-05-08       Impact factor: 4.064

2.  The immune microenvironment and expression of PD-L1, PD-1, PRAME and MHC I in salivary duct carcinoma.

Authors:  Bin Xu; Achim A Jungbluth; Denise Frosina; Bayan Alzumaili; Nathaniel Aleynick; Elzbieta Slodkowska; Kevin Higgins; Alan Ho; Luc Morris; Ronald Ghossein; Nora Katabi
Journal:  Histopathology       Date:  2019-10-02       Impact factor: 5.087

Review 3.  Pharmacologic inhibition of ataxia telangiectasia and Rad3-related (ATR) in the treatment of head and neck squamous cell carcinoma.

Authors:  Pooja Karukonda; Diana Odhiambo; Yvonne M Mowery
Journal:  Mol Carcinog       Date:  2021-12-29       Impact factor: 4.784

Review 4.  [Mode of action, new targets and potential biomarkers in modern immunotherapy].

Authors:  J Bedke; V Stühler; T Todenhöfer; A Stenzl
Journal:  Urologe A       Date:  2018-11       Impact factor: 0.639

Review 5.  Targeting Senescent Cells in Fibrosis: Pathology, Paradox, and Practical Considerations.

Authors:  Marissa J Schafer; Andrew J Haak; Daniel J Tschumperlin; Nathan K LeBrasseur
Journal:  Curr Rheumatol Rep       Date:  2018-01-26       Impact factor: 4.592

Review 6.  Hyperprogressive disease in patients with non-small cell lung cancer on immunotherapy.

Authors:  Jonathan S Kurman; Septimiu D Murgu
Journal:  J Thorac Dis       Date:  2018-02       Impact factor: 2.895

7.  Integrative Genome-Wide Analysis of Long Noncoding RNAs in Diverse Immune Cell Types of Melanoma Patients.

Authors:  Lei Wang; Sara J Felts; Virginia P Van Keulen; Adam D Scheid; Matthew S Block; Svetomir N Markovic; Larry R Pease; Yuji Zhang
Journal:  Cancer Res       Date:  2018-06-12       Impact factor: 12.701

Review 8.  Novel treatment strategies for patients with HER2-positive breast cancer who do not benefit from current targeted therapy drugs.

Authors:  Nan Jiang; Jing-Jing Lin; Jun Wang; Bei-Ning Zhang; Ao Li; Zheng-Yang Chen; Song Guo; Bin-Bin Li; Yu-Zhong Duan; Ru-Yi Yan; Hong-Feng Yan; Xiao-Yan Fu; Jin-Lian Zhou; He-Ming Yang; Yan Cui
Journal:  Exp Ther Med       Date:  2018-07-17       Impact factor: 2.447

9.  Intrinsic cell-penetrating activity propels Omomyc from proof of concept to viable anti-MYC therapy.

Authors:  Marie-Eve Beaulieu; Toni Jauset; Daniel Massó-Vallés; Sandra Martínez-Martín; Peter Rahl; Loïka Maltais; Mariano F Zacarias-Fluck; Sílvia Casacuberta-Serra; Erika Serrano Del Pozo; Christopher Fiore; Laia Foradada; Virginia Castillo Cano; Meritxell Sánchez-Hervás; Matthew Guenther; Eduardo Romero Sanz; Marta Oteo; Cynthia Tremblay; Génesis Martín; Danny Letourneau; Martin Montagne; Miguel Ángel Morcillo Alonso; Jonathan R Whitfield; Pierre Lavigne; Laura Soucek
Journal:  Sci Transl Med       Date:  2019-03-20       Impact factor: 17.956

10.  PD-L1 expression in colon cancer and its relationship with clinical prognosis.

Authors:  Tao Shan; Shuo Chen; Tao Wu; Yi Yang; Shunle Li; Xi Chen
Journal:  Int J Clin Exp Pathol       Date:  2019-05-01
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