Center for Molecular Medicine, University Medical Center Utrecht, Utrecht, the Netherlands.
Center for Molecular Medicine, University Medical Center Utrecht, Utrecht, the Netherlands; Department of Pathology, Radboud university medical center, Nijmegen, the Netherlands.
Biochim Biophys Acta Rev Cancer. 2022 May;1877(3):188719. doi: 10.1016/j.bbcan.2022.188719. Epub 2022 Mar 17.
Gastric cancer is globally the fourth leading cause of cancer-related deaths. Patients with diffuse-type gastric cancer (DGC) particularly have a poor prognosis that only marginally improved over the last decades, as conventional chemotherapies are frequently ineffective and specific therapies are unavailable. Early-stage DGC is characterized by intramucosal lesions of discohesive cells, which can be present for many years before the emergence of advanced DGC consisting of highly proliferative and invasive cells. The mechanisms underlying the key steps of DGC development and transition to aggressive tumors are starting to emerge. Novel mouse and organoid models for DGC, together with multi-omic analyses of DGC tumors, revealed contributions of both tumor cell-intrinsic alterations and gradual changes in the tumor microenvironment to DGC progression. In this review, we will discuss how these recent findings are leading towards an understanding of the cellular and molecular mechanisms responsible for DGC initiation and malignancy, which may provide opportunities for targeted therapies.
胃癌是全球导致癌症相关死亡的第四大主要原因。弥漫型胃癌(DGC)患者的预后尤其差,尽管在过去几十年中略有改善,但由于常规化疗通常无效且缺乏特异性疗法,这种情况并未得到改变。早期 DGC 的特征是离散细胞的黏膜内病变,这些病变在出现由高度增殖和侵袭性细胞组成的晚期 DGC 之前可能已经存在多年。DGC 发展和向侵袭性肿瘤转变的关键步骤背后的机制开始显现。用于 DGC 的新型小鼠和类器官模型以及对 DGC 肿瘤的多组学分析表明,肿瘤细胞内在改变和肿瘤微环境的逐渐变化都对 DGC 的进展有贡献。在这篇综述中,我们将讨论这些最新发现如何帮助我们理解导致 DGC 发生和恶性的细胞和分子机制,这可能为靶向治疗提供机会。