Modeling historic incidence trends implies early field cancerization in esophageal squamous cell carcinoma.

Patterns of cancer incidence, viewed over extended time periods, reveal important aspects of multistage carcinogenesis. Here we show how a multistage clonal expansion (MSCE) model for cancer can be harnessed to identify biological processes that shape the surprisingly dynamic and disparate incidence...

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Main Authors: Georg E Luebeck, Thomas L Vaughan, Kit Curtius, William D Hazelton
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2021-05-01
Series:PLoS Computational Biology
Online Access:https://journals.plos.org/ploscompbiol/article/file?id=10.1371/journal.pcbi.1008961&type=printable
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author Georg E Luebeck
Thomas L Vaughan
Kit Curtius
William D Hazelton
author_facet Georg E Luebeck
Thomas L Vaughan
Kit Curtius
William D Hazelton
author_sort Georg E Luebeck
collection DOAJ
description Patterns of cancer incidence, viewed over extended time periods, reveal important aspects of multistage carcinogenesis. Here we show how a multistage clonal expansion (MSCE) model for cancer can be harnessed to identify biological processes that shape the surprisingly dynamic and disparate incidence patterns of esophageal squamous cell carcinoma (ESCC) in the US population. While the dramatic rise in esophageal adenocarcinoma (EAC) in the US has been largely attributed to reflux related increases in the prevalence of Barrett's esophagus (BE), the premalignant field in which most EAC are thought to arise, only scant evidence exists for field cancerization contributing to ESCC. Our analyses of incidence patterns suggest that ESCC is associated with a premalignant field that may develop very early in life. Although the risk of ESCC, which is substantially higher in Blacks than Whites, is generally assumed to be associated with late-childhood and adult exposures to carcinogens, such as from tobacco smoking, alcohol consumption and various industrial exposures, the temporal trends we identify for ESCC suggest an onset distribution of field-defects before age 10, most strongly among Blacks. These trends differ significantly in shape and strength from field-defect trends that we estimate for US Whites. Moreover, the rates of ESCC-predisposing field-defects predicted by the model for cohorts of black children are decreasing for more recent birth cohorts (for Blacks born after 1940). These results point to a potential etiologic role of factors acting early in life, perhaps related to nutritional deficiencies, in the development of ESCC and its predisposing field-defect. Such factors may explain some of the striking racial differences seen in ESCC incidence patterns over time in the US.
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spelling doaj-art-933bcd9832fc4c53bfa8ba5520dd0f722025-08-20T02:01:03ZengPublic Library of Science (PLoS)PLoS Computational Biology1553-734X1553-73582021-05-01175e100896110.1371/journal.pcbi.1008961Modeling historic incidence trends implies early field cancerization in esophageal squamous cell carcinoma.Georg E LuebeckThomas L VaughanKit CurtiusWilliam D HazeltonPatterns of cancer incidence, viewed over extended time periods, reveal important aspects of multistage carcinogenesis. Here we show how a multistage clonal expansion (MSCE) model for cancer can be harnessed to identify biological processes that shape the surprisingly dynamic and disparate incidence patterns of esophageal squamous cell carcinoma (ESCC) in the US population. While the dramatic rise in esophageal adenocarcinoma (EAC) in the US has been largely attributed to reflux related increases in the prevalence of Barrett's esophagus (BE), the premalignant field in which most EAC are thought to arise, only scant evidence exists for field cancerization contributing to ESCC. Our analyses of incidence patterns suggest that ESCC is associated with a premalignant field that may develop very early in life. Although the risk of ESCC, which is substantially higher in Blacks than Whites, is generally assumed to be associated with late-childhood and adult exposures to carcinogens, such as from tobacco smoking, alcohol consumption and various industrial exposures, the temporal trends we identify for ESCC suggest an onset distribution of field-defects before age 10, most strongly among Blacks. These trends differ significantly in shape and strength from field-defect trends that we estimate for US Whites. Moreover, the rates of ESCC-predisposing field-defects predicted by the model for cohorts of black children are decreasing for more recent birth cohorts (for Blacks born after 1940). These results point to a potential etiologic role of factors acting early in life, perhaps related to nutritional deficiencies, in the development of ESCC and its predisposing field-defect. Such factors may explain some of the striking racial differences seen in ESCC incidence patterns over time in the US.https://journals.plos.org/ploscompbiol/article/file?id=10.1371/journal.pcbi.1008961&type=printable
spellingShingle Georg E Luebeck
Thomas L Vaughan
Kit Curtius
William D Hazelton
Modeling historic incidence trends implies early field cancerization in esophageal squamous cell carcinoma.
PLoS Computational Biology
title Modeling historic incidence trends implies early field cancerization in esophageal squamous cell carcinoma.
title_full Modeling historic incidence trends implies early field cancerization in esophageal squamous cell carcinoma.
title_fullStr Modeling historic incidence trends implies early field cancerization in esophageal squamous cell carcinoma.
title_full_unstemmed Modeling historic incidence trends implies early field cancerization in esophageal squamous cell carcinoma.
title_short Modeling historic incidence trends implies early field cancerization in esophageal squamous cell carcinoma.
title_sort modeling historic incidence trends implies early field cancerization in esophageal squamous cell carcinoma
url https://journals.plos.org/ploscompbiol/article/file?id=10.1371/journal.pcbi.1008961&type=printable
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AT thomaslvaughan modelinghistoricincidencetrendsimpliesearlyfieldcancerizationinesophagealsquamouscellcarcinoma
AT kitcurtius modelinghistoricincidencetrendsimpliesearlyfieldcancerizationinesophagealsquamouscellcarcinoma
AT williamdhazelton modelinghistoricincidencetrendsimpliesearlyfieldcancerizationinesophagealsquamouscellcarcinoma