Matsuoka Tasuku, Yashiro Masakazu
Molecular Oncology and Therapeutics, Osaka Metropolitan University Graduate School of Medicine, Osaka 5458585, Japan.
Cancers (Basel). 2023 Dec 21;16(1):54. doi: 10.3390/cancers16010054.
Gastric cancer (GC) is one of the most common malignancies worldwide. There has been no efficient therapy for stage IV GC patients due to this disease's heterogeneity and dissemination ability. Despite the rapid advancement of molecular targeted therapies, such as HER2 and immune checkpoint inhibitors, survival of GC patients is still unsatisfactory because the understanding of the mechanism of GC progression is still incomplete. Invasion is the most important feature of GC metastasis, which causes poor mortality in patients. Recently, genomic research has critically deepened our knowledge of which gene products are dysregulated in invasive GC. Furthermore, the study of the interaction of GC cells with the tumor microenvironment has emerged as a principal subject in driving invasion and metastasis. These results are expected to provide a profound knowledge of how biological molecules are implicated in GC development. This review summarizes the advances in our current understanding of the molecular mechanism of GC invasion. We also highlight the future directions of the invasion therapeutics of GC. Compared to conventional therapy using protease or molecular inhibitors alone, multi-therapy targeting invasion plasticity may seem to be an assuring direction for the progression of novel strategies.
胃癌(GC)是全球最常见的恶性肿瘤之一。由于该疾病的异质性和扩散能力,IV期胃癌患者一直没有有效的治疗方法。尽管分子靶向治疗(如HER2和免疫检查点抑制剂)迅速发展,但胃癌患者的生存率仍然不尽人意,因为对胃癌进展机制的理解仍不完整。侵袭是胃癌转移的最重要特征,这导致患者死亡率很高。最近,基因组研究极大地加深了我们对侵袭性胃癌中哪些基因产物失调的认识。此外,对胃癌细胞与肿瘤微环境相互作用的研究已成为驱动侵袭和转移的主要课题。这些结果有望为生物分子如何参与胃癌发展提供深刻的认识。本综述总结了我们目前对胃癌侵袭分子机制的理解进展。我们还强调了胃癌侵袭治疗的未来方向。与单独使用蛋白酶或分子抑制剂的传统治疗相比,针对侵袭可塑性的多疗法似乎是新策略进展的一个可靠方向。