Literature DB >> 32939993

The tumour immune landscape and its implications in cutaneous melanoma.

Grace H Attrill1,2, Peter M Ferguson1,2,3, Umaimainthan Palendira1,4, Georgina V Long1,2,5, James S Wilmott1,2, Richard A Scolyer1,2,3.   

Abstract

The field of tumour immunology has rapidly advanced in the last decade, leading to the advent of effective immunotherapies for patients with advanced cancers. This highlights the critical role of the immune system in determining tumour development and outcome. The tumour immune microenvironment (TIME) is highly heterogeneous, and the interactions between tumours and the immune system are vastly complex. Studying immune cell function in the TIME will provide an improved understanding of the mechanisms underpinning these interactions. This review examines the role of immune cell populations in the TIME based on their phenotype, function and localisation, as well as contextualising their position in the dynamic relationship between tumours and the immune system. We discuss the function of immune cell populations, examine their impact on patient outcome and highlight gaps in current understanding of their roles in the TIME, both in cancers in general and specifically in melanoma. Studying the TIME by evaluating both pro-tumour and anti-tumour effects may elucidate the conditions which lead to tumour growth and metastasis or immune-mediated tumour regression. Moreover, an in-depth understanding of these conditions could contribute to improved prognostication, more effective use of current immunotherapies and guide the development of novel treatment strategies and therapies.
© 2020 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

Entities:  

Keywords:  TILs; immunology; lymphocytes; melanoma; tumour microenvironment

Mesh:

Year:  2020        PMID: 32939993     DOI: 10.1111/pcmr.12926

Source DB:  PubMed          Journal:  Pigment Cell Melanoma Res        ISSN: 1755-1471            Impact factor:   4.693


  7 in total

1.  Using Immune-Related lncRNA Signature for Prognosis and Response to Immunotherapy in Cutaneous Melanoma.

Authors:  Ling Xue; Pingfan Wu; Xiaowen Zhao; Xiaojie Jin; Jingjing Wang; Yuxiang Shi; Xiaojing Yang; Yali She; Yaling Li; Changtian Li
Journal:  Int J Gen Med       Date:  2021-10-08

2.  Validation of an Accurate Automated Multiplex Immunofluorescence Method for Immuno-Profiling Melanoma.

Authors:  Zarwa Yaseen; Tuba N Gide; Jordan W Conway; Alison J Potter; Camelia Quek; Angela M Hong; Georgina V Long; Richard A Scolyer; James S Wilmott
Journal:  Front Mol Biosci       Date:  2022-05-19

3.  High expression of lncRNA HSD11B1-AS1 indicates favorable prognosis and is associated with immune infiltration in cutaneous melanoma.

Authors:  Kaiyuan Liu; Li Zhang; Xiuli Li; Jingjun Zhao
Journal:  Oncol Lett       Date:  2021-12-20       Impact factor: 2.967

4.  Identification and Construction of a Predictive Immune-Related lncRNA Signature Model for Melanoma.

Authors:  Fang-Wei Li; Sheng-Kang Luo
Journal:  Int J Gen Med       Date:  2021-12-01

5.  Analyzing Prognostic Hub Genes in the Microenvironment of Cutaneous Melanoma by Computer Integrated Bioinformatics.

Authors:  Guangyao Li; Jingye Zhang; Yourao Liu; Xiqing Cheng; Kai Sun; Wenjuan Hong; Ke Sha
Journal:  Comput Intell Neurosci       Date:  2022-03-08

Review 6.  Clinical features, molecular pathology, and immune microenvironmental characteristics of acral melanoma.

Authors:  Jianping Gui; Zhen Guo; Di Wu
Journal:  J Transl Med       Date:  2022-08-16       Impact factor: 8.440

7.  Detailed spatial immunophenotyping of primary melanomas reveals immune cell subpopulations associated with patient outcome.

Authors:  Grace H Attrill; Hansol Lee; Annie T Tasker; Nurudeen A Adegoke; Angela L Ferguson; Ines Pires da Silva; Robyn P M Saw; John F Thompson; Umaimainthan Palendira; Georgina V Long; Peter M Ferguson; Richard A Scolyer; James S Wilmott
Journal:  Front Immunol       Date:  2022-08-08       Impact factor: 8.786

  7 in total

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