trop -2细胞,它们的外泌体货物,以及对乳腺癌诊断和治疗的潜在影响:不断扩大的前沿

V. Kok
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引用次数: 0

摘要

乳房、卵巢和子宫内膜。3,4显然,这种Trop-2基因的上调为Trop-2过表达的癌细胞提供了选择性优势。虽然需要进一步的研究来提供更多的证据,但Trop-2基因的过表达可能与细胞膜和细胞质内Trop-2蛋白的丰度有关,这可以通过病理切片的免疫组织化学染色来检测。5,6 Trop-2糖蛋白参与癌细胞与细胞之间以及细胞与细胞外基质之间的通讯。因此,癌细胞可以在肿瘤微环境中迁移并具有侵袭性。此外,在过去的十年中,该领域的研究提供了一些重要的见解,即Trop2在组织坏死因子-α-转换酶(TACE,也称为ADAM17)的裂解和通过细胞外纤维连接蛋白激活β -1 (β 1)整合素依赖的迁移中起核心作用,其中主要受体主要是α 5 β 1 (α 5 β 1)整合素与细胞内局灶黏附激酶组装。最近,一种靶向Trop-2阳性癌细胞的抗滋养细胞表面抗原-2 (Trop-2)抗体-药物偶联物已被批准用于治疗无法切除的局部晚期或转移性三阴性乳腺癌患者,这些患者已接受两种或两种以上的全身化疗失败。这重新燃起了人们对Trop-2阳性乳腺癌、TACSTD2基因及其相互作用的microrna以及由Trop-2介导的信号传导引发的信号网络的转化研究的兴趣。此外,这篇观点论文认为,从Trop-2阳性癌细胞释放的细胞外囊泡外泌体可能在癌症进展中发挥重要作用。此外,利用trop -2释放的外泌体(货物外泌体携带的任何遗传信息,如特异性mirna、粘附分子(如整合素)和代谢物)在乳腺癌患者中的诊断应用尚待探索。大多数证据和数据来自于对上皮性癌症的研究,而不是乳腺癌,这在本文中已经介绍过。因此,本文简要总结了之前发表的其他癌症类型的数据,形成了一些假设,并提出了可能进一步探索的研究问题和方向。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Trop-2-Cells, Their Exosomal Cargo, and the Potential Impact on Diagnostics and Therapeutics in Breast Cancer: The Expanding Frontiers
breast, ovary, and endometrium. 3,4 Appar-ently, this Trop-2 gene upregulation provides selective advantages for Trop-2 overexpressing cancer cells. Although further research would be needed to provide more evidence, Trop-2 gene overexpression would correlate with the abundance of the Trop-2 protein on the cell membrane and inside the cytoplasm, which could be detected using immunohistochemical staining of a pathological slide. 5,6 Trop-2 glycoproteins are involved in the cancer cell-cell as well as cell-extracellular matrix communications. As a result, cancer cells could migrate and possess invasive properties within the tumor microenvironment. Furthermore, research in this arena in the past decade has provided some crucial insights that Trop2 plays a central role in the cleavage by tissue necrosis factor-α-converting enzyme (TACE, also known as ADAM17) and activating Beta-1 (β 1 ) integrin-dependent migration through extracellular fibronectin of which the main receptors are primarily Alpha 5 beta 1 (α 5 β 1 ) integrins assembling with the intracellular focal adhesion kinase. 7–10 This cascade of interactions and activations would ul-Trop-2-Cells, Abstract Recently, an anti-trophoblast surface antigen-2 (Trop-2) antibody-drug conjugate targeting Trop-2 positive cancer cells has been approved for treating patients with unresectable locally advanced or metastatic triple-negative breast cancer, who have failed two or more lines of systemic chemotherapy. This has renewed the interest in translational research of Trop-2 positive breast cancer, the gene TACSTD2 and microRNAs that interact with it, and the signaling networks sparked by Trop-2 mediated signaling. In addi-tion, this opinion paper argues that exosomes, extracellular vesicles that are released from Trop-2 positive cancer cells, could play a significant role in cancer progression. Furthermore, diagnostic applications using Trop-2-released exosomes, the cargo exosomes carry, which could be any genetic information such as specific miRNAs, adhesion molecules such as integrins, and metabolites, are yet to be explored in breast cancer patients. Most of the evidence and data are obtained from studies in epithelial cancers other than breast cancers, which have been introduced in the current paper. Therefore, this article briefly summarizes previously published data on other cancer types, forms some hypotheses, and proposes research questions and directions that may be explored further.
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