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Article: Immune related biomarkers for cancer metastasis to the brain

TitleImmune related biomarkers for cancer metastasis to the brain
Authors
KeywordsBrain metastasis
Immune biomarkers
Systemic tumor immune environment
Tumor immune microenvironment
Issue Date2022
Citation
Experimental Hematology and Oncology, 2022, v. 11 n. 1, article no. 105 How to Cite?
AbstractBrain metastasis accounts for a large number of cancer-related deaths. The host immune system, involved at each step of the metastatic cascade, plays an important role in both the initiation of the brain metastasis and their treatment responses to various modalities, through either local and or systemic effect. However, few reliable immune biomarkers have been identified in predicting the development and the treatment outcome in patients with cancer brain metastasis. Here, we provide a focused perspective of immune related biomarkers for cancer metastasis to the brain and a thorough discussion of the potential utilization of specific biomarkers such as tumor mutation burden (TMB), genetic markers, circulating and tumor-infiltrating immune cells, cytokines, in predicting the brain disease progression and regression after therapeutic intervention. We hope to inspire the field to extend the research and establish practical guidelines for developing and validating immune related biomarkers to provide personalized treatment and improve treatment outcomes in patients with metastatic brain cancers.
Persistent Identifierhttp://hdl.handle.net/10722/323639
PubMed Central ID
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorCHEN, W-
dc.contributor.authorChu, TSM-
dc.contributor.authorXu, L-
dc.contributor.authorZHAO, C-
dc.contributor.authorPoon, WS-
dc.contributor.authorLeung, GKK-
dc.contributor.authorKong, FP-
dc.date.accessioned2023-01-08T07:10:10Z-
dc.date.available2023-01-08T07:10:10Z-
dc.date.issued2022-
dc.identifier.citationExperimental Hematology and Oncology, 2022, v. 11 n. 1, article no. 105-
dc.identifier.urihttp://hdl.handle.net/10722/323639-
dc.description.abstractBrain metastasis accounts for a large number of cancer-related deaths. The host immune system, involved at each step of the metastatic cascade, plays an important role in both the initiation of the brain metastasis and their treatment responses to various modalities, through either local and or systemic effect. However, few reliable immune biomarkers have been identified in predicting the development and the treatment outcome in patients with cancer brain metastasis. Here, we provide a focused perspective of immune related biomarkers for cancer metastasis to the brain and a thorough discussion of the potential utilization of specific biomarkers such as tumor mutation burden (TMB), genetic markers, circulating and tumor-infiltrating immune cells, cytokines, in predicting the brain disease progression and regression after therapeutic intervention. We hope to inspire the field to extend the research and establish practical guidelines for developing and validating immune related biomarkers to provide personalized treatment and improve treatment outcomes in patients with metastatic brain cancers.-
dc.languageeng-
dc.relation.ispartofExperimental Hematology and Oncology-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.subjectBrain metastasis-
dc.subjectImmune biomarkers-
dc.subjectSystemic tumor immune environment-
dc.subjectTumor immune microenvironment-
dc.titleImmune related biomarkers for cancer metastasis to the brain-
dc.typeArticle-
dc.identifier.emailLeung, GKK: gkkleung@hku.hk-
dc.identifier.emailKong, FP: kong0001@hku.hk-
dc.identifier.authorityLeung, GKK=rp00522-
dc.identifier.authorityKong, FP=rp02508-
dc.description.naturepublished_or_final_version-
dc.identifier.doi10.1186/s40164-022-00349-z-
dc.identifier.pmid36527157-
dc.identifier.pmcidPMC9756766-
dc.identifier.scopuseid_2-s2.0-85144116847-
dc.identifier.hkuros343183-
dc.identifier.volume11-
dc.identifier.issue1-
dc.identifier.spagearticle no. 105-
dc.identifier.epagearticle no. 105-
dc.identifier.eissn2162-3619-
dc.identifier.isiWOS:000895884600001-

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