Department of Oncology, University of Oxford, Oxford OX3 7DQ, United Kingdom.
Institute of Molecular Biology and Biotechnologies, Ministry of Science and Education of the Republic of Azerbaijan, Baku AZ1073, Azerbaijan.
Proc Natl Acad Sci U S A. 2024 Oct 22;121(43):e2414213121. doi: 10.1073/pnas.2414213121. Epub 2024 Oct 14.
The poor prognosis of relatively undifferentiated cancers has long been recognized, suggesting that selection against differentiation and in favor of uncontrolled growth is one of the most powerful drivers of cancer progression. Goblet cells provide the mucous surface of the gut, and when present in colorectal cancers (CRC), the cancers are called mucinous. We have used the presence of MUC2, the main mucous product of goblet cells, and an associated gene product, TFF3, to classify a large panel of nearly 80 CRC-derived cell lines into five categories based on their levels of MUC2 and TFF3 expression. We have then shown that these five patterns of expression can be easily identified in the direct analysis of tumor specimens allowing a much finer characterization of CRCs with respect to the presence of goblet cell differentiation. In particular, about 30% of all CRCs fall into the category of expressing TFF3 but not MUC2, which has not previously been acknowledged. Using the cell line data, we suggest that there are up to 12 genes ( and ) that may be involved in selection against goblet cell differentiation in CRC by changes in methylation rather than mutations. Of these, , which is particularly associated with lack of goblet cell features, may function in the control of differentiation rather than direct control of cell growth, as has so far mostly been assumed. These results emphasize the importance of methylation changes in driving cancer progression.
长期以来,人们一直认识到相对未分化癌症的预后较差,这表明分化选择的缺失和不受控制的生长是癌症进展的最强大驱动力之一。杯状细胞提供肠道的黏液表面,当存在于结直肠癌 (CRC) 中时,这些癌症被称为黏液性。我们使用主要的杯状细胞黏液产物 MUC2 和相关基因产物 TFF3 的存在,根据其 MUC2 和 TFF3 表达水平,将近 80 种源自 CRC 的细胞系的大型面板分类为五类。然后,我们表明这些五种表达模式可以在肿瘤标本的直接分析中轻松识别,从而可以更精细地对 CRC 进行特征描述,以确定是否存在杯状细胞分化。特别是,大约 30%的所有 CRC 属于表达 TFF3 但不表达 MUC2 的类别,这以前尚未得到承认。使用细胞系数据,我们建议有多达 12 个基因(和)可能通过甲基化而不是突变来参与 CRC 中对杯状细胞分化的选择缺失。其中,与缺乏杯状细胞特征特别相关的,可能在分化控制中发挥作用,而不是像迄今为止大多数人假设的那样直接控制细胞生长。这些结果强调了甲基化变化在推动癌症进展中的重要性。