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Ethnic differences in hepatocellular carcinoma prevalence and therapeutic outcomes
BACKGROUND: Hepatocellular carcinoma (HCC) is a leading cause of cancer‐related death worldwide. The incidence of HCC is affected by genetic and non‐genetic factors. Genetically, mutations in the genes, tumor protein P53 (TP53), catenin beta 1 (CTNNB1), AT‐rich interaction domain 1A (ARIC1A), cyclin...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10440848/ https://www.ncbi.nlm.nih.gov/pubmed/37344125 http://dx.doi.org/10.1002/cnr2.1821 |
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author | Chavda, Vivek Zajac, Kelsee K. Gunn, Jenna Lynn Balar, Pankti Khadela, Avinash Vaghela, Dixa Soni, Shruti Ashby, Charles R. Tiwari, Amit K. |
author_facet | Chavda, Vivek Zajac, Kelsee K. Gunn, Jenna Lynn Balar, Pankti Khadela, Avinash Vaghela, Dixa Soni, Shruti Ashby, Charles R. Tiwari, Amit K. |
author_sort | Chavda, Vivek |
collection | PubMed |
description | BACKGROUND: Hepatocellular carcinoma (HCC) is a leading cause of cancer‐related death worldwide. The incidence of HCC is affected by genetic and non‐genetic factors. Genetically, mutations in the genes, tumor protein P53 (TP53), catenin beta 1 (CTNNB1), AT‐rich interaction domain 1A (ARIC1A), cyclin dependent kinase inhibitor 2A (CDKN2A), mannose 6‐phosphate (M6P), smooth muscle action against decapentaplegic (SMAD2), retinoblastoma gene (RB1), cyclin D, antigen presenting cells (APC), AXIN1, and E‐cadherin, have been shown to contribute to the occurrence of HCC. Non‐genetic factors, including alcohol consumption, exposure to aflatoxin, age, gender, presence of hepatitis B (HBV), hepatitis C (HCV), and non‐alcoholic fatty liver disease (NAFLD), increase the risk of HCC. RECENT FINDINGS: The severity of the disease and its occurrence vary based on geographical location. Furthermore, men and minorities have been shown to be disproportionately affected by HCC, compared with women and non‐minorities. Ethnicity has been reported to significantly affect tumorigenesis and clinical outcomes in patients diagnosed with HCC. Generally, differences in gene expression and/or the presence of comorbid medical diseases affect or influence the progression of HCC. Non‐Caucasian HCC patients are significantly more likely to have poorer survival outcomes, compared to their Caucasian counterparts. Finally, there are a number of factors that contribute to the success rate of treatments for HCC. CONCLUSION: Assessment and treatment of HCC must be consistent using evidence‐based guidelines and standardized outcomes, as well as international clinical practice guidelines for global consensus. Standardizing the assessment approach and method will enable comparison and improvement of liver cancer research through collaboration between researchers, healthcare providers, and advocacy groups. In this review, we will focus on discussing epidemiological factors that result in deviations and changes in treatment approaches for HCC. |
format | Online Article Text |
id | pubmed-10440848 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-104408482023-08-22 Ethnic differences in hepatocellular carcinoma prevalence and therapeutic outcomes Chavda, Vivek Zajac, Kelsee K. Gunn, Jenna Lynn Balar, Pankti Khadela, Avinash Vaghela, Dixa Soni, Shruti Ashby, Charles R. Tiwari, Amit K. Cancer Rep (Hoboken) The publication of this supplement has been funded by Gilead Sciences, Inc. BACKGROUND: Hepatocellular carcinoma (HCC) is a leading cause of cancer‐related death worldwide. The incidence of HCC is affected by genetic and non‐genetic factors. Genetically, mutations in the genes, tumor protein P53 (TP53), catenin beta 1 (CTNNB1), AT‐rich interaction domain 1A (ARIC1A), cyclin dependent kinase inhibitor 2A (CDKN2A), mannose 6‐phosphate (M6P), smooth muscle action against decapentaplegic (SMAD2), retinoblastoma gene (RB1), cyclin D, antigen presenting cells (APC), AXIN1, and E‐cadherin, have been shown to contribute to the occurrence of HCC. Non‐genetic factors, including alcohol consumption, exposure to aflatoxin, age, gender, presence of hepatitis B (HBV), hepatitis C (HCV), and non‐alcoholic fatty liver disease (NAFLD), increase the risk of HCC. RECENT FINDINGS: The severity of the disease and its occurrence vary based on geographical location. Furthermore, men and minorities have been shown to be disproportionately affected by HCC, compared with women and non‐minorities. Ethnicity has been reported to significantly affect tumorigenesis and clinical outcomes in patients diagnosed with HCC. Generally, differences in gene expression and/or the presence of comorbid medical diseases affect or influence the progression of HCC. Non‐Caucasian HCC patients are significantly more likely to have poorer survival outcomes, compared to their Caucasian counterparts. Finally, there are a number of factors that contribute to the success rate of treatments for HCC. CONCLUSION: Assessment and treatment of HCC must be consistent using evidence‐based guidelines and standardized outcomes, as well as international clinical practice guidelines for global consensus. Standardizing the assessment approach and method will enable comparison and improvement of liver cancer research through collaboration between researchers, healthcare providers, and advocacy groups. In this review, we will focus on discussing epidemiological factors that result in deviations and changes in treatment approaches for HCC. John Wiley and Sons Inc. 2023-06-21 /pmc/articles/PMC10440848/ /pubmed/37344125 http://dx.doi.org/10.1002/cnr2.1821 Text en © 2023 The Authors. Cancer Reports published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | The publication of this supplement has been funded by Gilead Sciences, Inc. Chavda, Vivek Zajac, Kelsee K. Gunn, Jenna Lynn Balar, Pankti Khadela, Avinash Vaghela, Dixa Soni, Shruti Ashby, Charles R. Tiwari, Amit K. Ethnic differences in hepatocellular carcinoma prevalence and therapeutic outcomes |
title | Ethnic differences in hepatocellular carcinoma prevalence and therapeutic outcomes |
title_full | Ethnic differences in hepatocellular carcinoma prevalence and therapeutic outcomes |
title_fullStr | Ethnic differences in hepatocellular carcinoma prevalence and therapeutic outcomes |
title_full_unstemmed | Ethnic differences in hepatocellular carcinoma prevalence and therapeutic outcomes |
title_short | Ethnic differences in hepatocellular carcinoma prevalence and therapeutic outcomes |
title_sort | ethnic differences in hepatocellular carcinoma prevalence and therapeutic outcomes |
topic | The publication of this supplement has been funded by Gilead Sciences, Inc. |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10440848/ https://www.ncbi.nlm.nih.gov/pubmed/37344125 http://dx.doi.org/10.1002/cnr2.1821 |
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