Cancer Stem Cell Laboratory, The Breast Cancer Now Toby Robins Research Centre, Institute of Cancer Research, London, SW3 6JB, UK.
CRUK Beatson Institute, G61 1BD, Glasgow, UK.
Oncogene. 2022 Oct;41(42):4686-4695. doi: 10.1038/s41388-022-02448-x. Epub 2022 Sep 10.
Intratumour heterogeneity (ITH) has become an important focus of cancer research in recent years. ITH describes the cellular variation that enables tumour evolution, including tumour progression, metastasis and resistance to treatment. The selection and expansion of genetically distinct treatment-resistant cancer cell clones provides one explanation for treatment failure. However, tumour cell variation need not be genetically encoded. In pancreatic ductal adenocarcinoma (PDAC) in particular, the complex tumour microenvironment as well as crosstalk between tumour and stromal cells result in exceptionally variable tumour cell phenotypes that are also highly adaptable. In this review we discuss four different types of phenotypic heterogeneity within PDAC, from morphological to metabolic heterogeneity. We suggest that these different types of ITH are not independent, but, rather, can inform one another. Lastly, we highlight recent findings that suggest how therapeutic efforts may halt PDAC progression by constraining cellular heterogeneity.
近年来,肿瘤内异质性(ITH)已成为癌症研究的一个重要焦点。ITH 描述了使肿瘤进化的细胞变异,包括肿瘤进展、转移和对治疗的耐药性。具有遗传异质性的治疗耐药性癌细胞克隆的选择和扩增为治疗失败提供了一种解释。然而,肿瘤细胞的变异不一定是遗传编码的。特别是在胰腺导管腺癌 (PDAC) 中,复杂的肿瘤微环境以及肿瘤细胞与基质细胞之间的相互作用,导致肿瘤细胞表型非常多变,而且适应性也很强。在这篇综述中,我们讨论了 PDAC 中四种不同类型的表型异质性,从形态学到代谢异质性。我们认为,这些不同类型的 ITH 不是独立的,而是可以相互提供信息。最后,我们强调了最近的发现,这些发现表明治疗努力如何通过限制细胞异质性来阻止 PDAC 的进展。