Suppr超能文献

胃癌中上皮-间质转化的抑制或逆转:药理学方法。

Inhibition or Reversal of the Epithelial-Mesenchymal Transition in Gastric Cancer: Pharmacological Approaches.

机构信息

Department of Human Anatomy, Medical University of Lublin, 20-090 Lublin, Poland.

Department of Forensic Medicine, Medical University of Lublin, 20-090 Lublin, Poland.

出版信息

Int J Mol Sci. 2020 Dec 29;22(1):277. doi: 10.3390/ijms22010277.

Abstract

Epithelial-mesenchymal transition (EMT) constitutes one of the hallmarks of carcinogenesis consisting in the re-differentiation of the epithelial cells into mesenchymal ones changing the cellular phenotype into a malignant one. EMT has been shown to play a role in the malignant transformation and while occurring in the tumor microenvironment, it significantly affects the aggressiveness of gastric cancer, among others. Importantly, after EMT occurs, gastric cancer patients are more susceptible to the induction of resistance to various therapeutic agents, worsening the clinical outcome of patients. Therefore, there is an urgent need to search for the newest pharmacological agents targeting EMT to prevent further progression of gastric carcinogenesis and potential metastases. Therapies targeted at EMT might be combined with other currently available treatment modalities, which seems to be an effective strategy to treat gastric cancer patients. In this review, we have summarized recent advances in gastric cancer treatment in terms of targeting EMT specifically, such as the administration of polyphenols, resveratrol, tangeretin, luteolin, genistein, proton pump inhibitors, terpenes, other plant extracts, or inorganic compounds.

摘要

上皮-间充质转化(EMT)是癌症发生的标志之一,它包括上皮细胞重新分化为间充质细胞,将细胞表型改变为恶性表型。EMT 已被证明在恶性转化中起作用,并且在肿瘤微环境中发生时,它会显著影响胃癌等的侵袭性。重要的是,EMT 发生后,胃癌患者更容易对各种治疗药物产生耐药性,从而恶化患者的临床预后。因此,迫切需要寻找针对 EMT 的新型药理学制剂,以防止胃肿瘤发生和潜在转移的进一步进展。针对 EMT 的治疗方法可能与其他目前可用的治疗方式相结合,这似乎是治疗胃癌患者的有效策略。在这篇综述中,我们总结了针对 EMT 的胃癌治疗的最新进展,例如多酚、白藜芦醇、桔皮素、木樨草素、染料木黄酮、质子泵抑制剂、萜类化合物、其他植物提取物或无机化合物的应用。

相似文献

2
Role of epithelial-mesenchymal transition in gastric cancer initiation and progression.
World J Gastroenterol. 2014 May 14;20(18):5403-10. doi: 10.3748/wjg.v20.i18.5403.
7
Cisplatin resistance in gastric cancer cells is involved with GPR30-mediated epithelial-mesenchymal transition.
J Cell Mol Med. 2020 Mar;24(6):3625-3633. doi: 10.1111/jcmm.15055. Epub 2020 Feb 12.
8
NANOGP8 is the key regulator of stemness, EMT, Wnt pathway, chemoresistance, and other malignant phenotypes in gastric cancer cells.
PLoS One. 2018 Apr 24;13(4):e0192436. doi: 10.1371/journal.pone.0192436. eCollection 2018.
9
Epithelial-mesenchymal transition confers resistance to selective FGFR inhibitors in SNU-16 gastric cancer cells.
Gastric Cancer. 2016 Jan;19(1):53-62. doi: 10.1007/s10120-014-0444-1. Epub 2014 Nov 19.

引用本文的文献

1
Epithelial-Mesenchymal Transition in Cancer: Insights Into Therapeutic Targets and Clinical Implications.
MedComm (2020). 2025 Aug 29;6(9):e70333. doi: 10.1002/mco2.70333. eCollection 2025 Sep.
4
Cellular and Molecular Mechanisms Modulated by Genistein in Cancer.
Int J Mol Sci. 2025 Jan 27;26(3):1114. doi: 10.3390/ijms26031114.
5
Prognostic significance of tumor budding, desmoplastic reaction, and lymphocytic infiltration in patients with gastric adenocarcinoma.
World J Gastrointest Pathophysiol. 2024 Apr 22;15(1):91237. doi: 10.4291/wjgp.v15.i1.91237.
6
Contribution of Autophagy to Epithelial Mesenchymal Transition Induction during Cancer Progression.
Cancers (Basel). 2024 Feb 16;16(4):807. doi: 10.3390/cancers16040807.
10
Research progress of sophoridine's pharmacological activities and its molecular mechanism: an updated review.
Front Pharmacol. 2023 Jun 16;14:1126636. doi: 10.3389/fphar.2023.1126636. eCollection 2023.

本文引用的文献

1
Gastric carcinogenesis: a comprehensive review of the angiogenic pathways.
Clin J Gastroenterol. 2021 Feb;14(1):14-25. doi: 10.1007/s12328-020-01295-1. Epub 2020 Nov 18.
6
Association of the Epithelial-Mesenchymal Transition (EMT) with Cisplatin Resistance.
Int J Mol Sci. 2020 Jun 3;21(11):4002. doi: 10.3390/ijms21114002.
9
The function of miR-200 family in oxidative stress response evoked in cancer chemotherapy and radiotherapy.
Biomed Pharmacother. 2020 May;125:110037. doi: 10.1016/j.biopha.2020.110037. Epub 2020 Feb 25.
10
Metformin as Potential Therapy for High-Grade Glioma.
Cancers (Basel). 2020 Jan 15;12(1):210. doi: 10.3390/cancers12010210.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验