Literature DB >> 25843228

Role of CD154 in cancer pathogenesis and immunotherapy.

Ghada S Hassan1, John Stagg1, Walid Mourad2.   

Abstract

Many factors and molecules have been investigated as potential players in the pathogenesis or immunosurveillance of cancer. Among these, CD154 has been recognized as a co-stimulatory molecule with high potential for treating cancer, in addition to its contribution in the development of the disease. CD154 was initially described for its pivotal role in T cell-dependent humoral responses via an interaction with its classical receptor, CD40. Subsequent studies showed that CD154 is also implicated in cell-mediated immunity and inflammation via an interaction with CD40 alone or in combination with newly identified receptors, members of the integrin family, leading to the development of chronic inflammatory and autoimmune diseases. In the current article, we present an overview of the role of CD154 as a potential etiological factor in tumors inducing proliferation of malignant cells, their rescue from apoptosis and their invasiveness. In addition, this review describes the immuno-regulatory functions of CD154 against cancer reflected by its stimulation of antigen-presenting cells and the subsequent activation of effector cells, its enhancement of malignant cells' immunogenicity, its modulation of immune settings around tumors, and its initiation of proliferation inhibiting effects in malignant cells. In vitro as well as in vivo studies are outlined and a particular attention is given to clinical studies and progress reached at this point. Findings reviewed herein will improve our knowledge of the role of the CD154 system in cancers from causative to immunotherapeutic functions, paving the way for the identification of new targets for prevention and/or treatment of malignant disorders.
Copyright © 2015 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Animal model; Apoptosis; CD154; CD40; Cancer; Clinical trial; Immune response; Proliferation

Mesh:

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Year:  2015        PMID: 25843228     DOI: 10.1016/j.ctrv.2015.03.007

Source DB:  PubMed          Journal:  Cancer Treat Rev        ISSN: 0305-7372            Impact factor:   12.111


  10 in total

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Authors:  Paul R Walker; Denis Migliorini
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2.  Local Induction of B Cell Interleukin-10 Competency Alleviates Inflammation and Bone Loss in Ligature-Induced Experimental Periodontitis in Mice.

Authors:  Pei Yu; Yang Hu; Zhiqiang Liu; Toshihisa Kawai; Martin A Taubman; Wei Li; Xiaozhe Han
Journal:  Infect Immun       Date:  2016-12-29       Impact factor: 3.441

Review 3.  Novel Functions of Integrins as Receptors of CD154: Their Role in Inflammation and Apoptosis.

Authors:  Ghada S Hassan; Suzanne Salti; Walid Mourad
Journal:  Cells       Date:  2022-05-25       Impact factor: 7.666

Review 4.  Recent Advances in ADAM17 Research: A Promising Target for Cancer and Inflammation.

Authors:  Marcia L Moss; Dmitry Minond
Journal:  Mediators Inflamm       Date:  2017-11-02       Impact factor: 4.711

5.  CD40L inhibits cell growth of THP-1 cells by suppressing the PI3K/Akt pathway.

Authors:  Zhongxin Feng; Qi Chen; Mingqiang Ren; Zuguo Tian; Yuping Gong
Journal:  Onco Targets Ther       Date:  2019-04-18       Impact factor: 4.147

6.  Raised CD40L expression attenuates drug resistance in Adriamycin-resistant THP-1 cells.

Authors:  Zhongxin Feng; Qi Chen
Journal:  Exp Ther Med       Date:  2020-01-15       Impact factor: 2.447

7.  Soluble CD40 ligand inhibits the growth of non-Hodgkin's lymphoma cells through the JNK signaling pathway.

Authors:  Zhongxin Feng; Jishi Wang
Journal:  Oncol Lett       Date:  2020-11-18       Impact factor: 2.967

8.  Levels of human platelet-derived soluble CD40 ligand depend on haplotypes of CD40LG-CD40-ITGA2.

Authors:  Chaker Aloui; Antoine Prigent; Sofiane Tariket; Caroline Sut; Jocelyne Fagan; Fabrice Cognasse; Tahar Chakroun; Olivier Garraud; Sandrine Laradi
Journal:  Sci Rep       Date:  2016-04-20       Impact factor: 4.379

9.  Soluble CD40 ligand directly alters glomerular permeability and may act as a circulating permeability factor in FSGS.

Authors:  Sophie Doublier; Cristina Zennaro; Luca Musante; Tiziana Spatola; Giovanni Candiano; Maurizio Bruschi; Luca Besso; Massimo Cedrino; Michele Carraro; Gian Marco Ghiggeri; Giovanni Camussi; Enrico Lupia
Journal:  PLoS One       Date:  2017-11-20       Impact factor: 3.240

10.  CCR2 signaling in breast carcinoma cells promotes tumor growth and invasion by promoting CCL2 and suppressing CD154 effects on the angiogenic and immune microenvironments.

Authors:  Gage Brummer; Wei Fang; Curtis Smart; Brandon Zinda; Nadia Alissa; Cory Berkland; David Miller; Nikki Cheng
Journal:  Oncogene       Date:  2019-12-11       Impact factor: 9.867

  10 in total

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