Public Health Sciences Division, Computational Biology Program, Fred Hutchinson Cancer Research Center, Seattle, Washington, United States of America.
Professor Emeritus, Public Health Sciences Division, Cancer Epidemiology Program, Fred Hutchinson Cancer Research Center, Seattle, Washington, United States of America.
PLoS Comput Biol. 2021 May 3;17(5):e1008961. doi: 10.1371/journal.pcbi.1008961. eCollection 2021 May.
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.
从长期来看,癌症发病率的模式揭示了多阶段致癌作用的重要方面。在这里,我们展示了如何利用癌症的多阶段克隆扩张(MSCE)模型来识别塑造美国人群中食管鳞状细胞癌(ESCC)惊人动态和不同发病率模式的生物学过程。虽然美国食管腺癌(EAC)的急剧上升在很大程度上归因于反流相关的 Barrett 食管(BE)患病率增加,这是大多数 EAC 被认为起源的癌前区域,但几乎没有证据表明癌前区域的癌变会导致 ESCC。我们对发病模式的分析表明,ESCC 与癌前区域相关,该区域可能在生命早期就已经发展。尽管 ESCC 的风险在黑人群体中明显高于白人群体,通常被认为与儿童后期和成年期接触致癌物质(如吸烟、饮酒和各种工业暴露)有关,但我们为 ESCC 确定的时间趋势表明,在 10 岁之前就已经出现了癌前缺陷的分布,黑人群体中这种情况最为明显。这些趋势在形状和强度上与我们为美国白人估计的癌前缺陷趋势有显著差异。此外,模型预测的黑人群体中易患 ESCC 的癌前缺陷发生率在最近出生的队列中(对于 1940 年后出生的黑人)正在下降。这些结果表明,在生命早期起作用的因素(可能与营养缺乏有关)可能在 ESCC 及其癌前缺陷的发展中起潜在的病因作用。这些因素可能解释了美国 ESCC 发病率模式随时间变化的一些显著的种族差异。