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Epidemiological characteristics and genetic alterations in adult diffuse glioma in East Asian populations

Understanding the racial specificities of diseases—such as adult diffuse glioma, the most common primary malignant tumor of the central nervous system—is a critical step toward precision medicine. Here, we comprehensively review studies of gliomas in East Asian populations and other ancestry groups...

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Autores principales: Mo, Zongchao, Xin, Junyi, Chai, Ruichao, Woo, Peter Y.M., Chan, Danny T.M., Wang, Jiguang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Compuscript 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9630523/
https://www.ncbi.nlm.nih.gov/pubmed/36350002
http://dx.doi.org/10.20892/j.issn.2095-3941.2022.0418
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author Mo, Zongchao
Xin, Junyi
Chai, Ruichao
Woo, Peter Y.M.
Chan, Danny T.M.
Wang, Jiguang
author_facet Mo, Zongchao
Xin, Junyi
Chai, Ruichao
Woo, Peter Y.M.
Chan, Danny T.M.
Wang, Jiguang
author_sort Mo, Zongchao
collection PubMed
description Understanding the racial specificities of diseases—such as adult diffuse glioma, the most common primary malignant tumor of the central nervous system—is a critical step toward precision medicine. Here, we comprehensively review studies of gliomas in East Asian populations and other ancestry groups to clarify the racial differences in terms of epidemiology and genomic characteristics. Overall, we observed a lower glioma incidence in East Asians than in Whites; notably, patients with glioblastoma had significantly younger ages of onset and longer overall survival than the Whites. Multiple genome-wide association studies of various cohorts have revealed single nucleotide polymorphisms associated with overall and subtype-specific glioma susceptibility. Notably, only 3 risk loci—5p15.33, 11q23.3, and 20q13.33—were shared between patients with East Asian and White ancestry, whereas other loci predominated only in particular populations. For instance, risk loci 12p11.23, 15q15-21.1, and 19p13.12 were reported in East Asians, whereas risk loci 8q24.21, 1p31.3, and 1q32.1 were reported in studies in White patients. Although the somatic mutational profiles of gliomas between East Asians and non-East Asians were broadly consistent, a lower incidence of EGFR amplification in glioblastoma and a higher incidence of 1p19q-IDH-TERT triple-negative low-grade glioma were observed in East Asian cohorts. By summarizing large-scale disease surveillance, germline, and somatic genomic studies, this review reveals the unique characteristics of adult diffuse glioma among East Asians, to guide clinical management and policy design focused on patients with East Asian ancestry.
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spelling pubmed-96305232022-11-07 Epidemiological characteristics and genetic alterations in adult diffuse glioma in East Asian populations Mo, Zongchao Xin, Junyi Chai, Ruichao Woo, Peter Y.M. Chan, Danny T.M. Wang, Jiguang Cancer Biol Med Review Understanding the racial specificities of diseases—such as adult diffuse glioma, the most common primary malignant tumor of the central nervous system—is a critical step toward precision medicine. Here, we comprehensively review studies of gliomas in East Asian populations and other ancestry groups to clarify the racial differences in terms of epidemiology and genomic characteristics. Overall, we observed a lower glioma incidence in East Asians than in Whites; notably, patients with glioblastoma had significantly younger ages of onset and longer overall survival than the Whites. Multiple genome-wide association studies of various cohorts have revealed single nucleotide polymorphisms associated with overall and subtype-specific glioma susceptibility. Notably, only 3 risk loci—5p15.33, 11q23.3, and 20q13.33—were shared between patients with East Asian and White ancestry, whereas other loci predominated only in particular populations. For instance, risk loci 12p11.23, 15q15-21.1, and 19p13.12 were reported in East Asians, whereas risk loci 8q24.21, 1p31.3, and 1q32.1 were reported in studies in White patients. Although the somatic mutational profiles of gliomas between East Asians and non-East Asians were broadly consistent, a lower incidence of EGFR amplification in glioblastoma and a higher incidence of 1p19q-IDH-TERT triple-negative low-grade glioma were observed in East Asian cohorts. By summarizing large-scale disease surveillance, germline, and somatic genomic studies, this review reveals the unique characteristics of adult diffuse glioma among East Asians, to guide clinical management and policy design focused on patients with East Asian ancestry. Compuscript 2022-10-15 2022-11-01 /pmc/articles/PMC9630523/ /pubmed/36350002 http://dx.doi.org/10.20892/j.issn.2095-3941.2022.0418 Text en Copyright: © 2022, Cancer Biology & Medicine https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (CC BY) 4.0 (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution and reproduction in any medium, provided the original author and source are credited.
spellingShingle Review
Mo, Zongchao
Xin, Junyi
Chai, Ruichao
Woo, Peter Y.M.
Chan, Danny T.M.
Wang, Jiguang
Epidemiological characteristics and genetic alterations in adult diffuse glioma in East Asian populations
title Epidemiological characteristics and genetic alterations in adult diffuse glioma in East Asian populations
title_full Epidemiological characteristics and genetic alterations in adult diffuse glioma in East Asian populations
title_fullStr Epidemiological characteristics and genetic alterations in adult diffuse glioma in East Asian populations
title_full_unstemmed Epidemiological characteristics and genetic alterations in adult diffuse glioma in East Asian populations
title_short Epidemiological characteristics and genetic alterations in adult diffuse glioma in East Asian populations
title_sort epidemiological characteristics and genetic alterations in adult diffuse glioma in east asian populations
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9630523/
https://www.ncbi.nlm.nih.gov/pubmed/36350002
http://dx.doi.org/10.20892/j.issn.2095-3941.2022.0418
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