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Xmrks 着点:鱼类模型在癌症研究中用于研究表皮生长因子受体信号通路。

Xmrks the Spot: Fish Models for Investigating Epidermal Growth Factor Receptor Signaling in Cancer Research.

机构信息

Department of Cell and Molecular Biology, Cancer Center and Research Institute, University of Mississippi Medical Center, 2500 North State Street, Jackson, MS 39216, USA.

School of Medicine, Deakin University, Locked Bag 20000, Geelong, VIC 3220, Australia.

出版信息

Cells. 2021 May 7;10(5):1132. doi: 10.3390/cells10051132.

Abstract

Studies conducted in several fish species, e.g., (green swordtail) and maculatus (southern platyfish) crosses, (medaka), and (zebrafish), have identified an oncogenic role for the receptor tyrosine kinase, Xmrk, a gene product closely related to the human epidermal growth factor receptor (EGFR), which is associated with a wide variety of pathological conditions, including cancer. Comparative analyses of Xmrk and EGFR signal transduction in melanoma have shown that both utilize STAT5 signaling to regulate apoptosis and cell proliferation, PI3K to modulate apoptosis, FAK to control migration, and the Ras/Raf/MEK/MAPK pathway to regulate cell survival, proliferation, and differentiation. Further, Xmrk and EGFR may also modulate similar chemokine, extracellular matrix, oxidative stress, and microRNA signaling pathways in melanoma. In hepatocellular carcinoma (HCC), Xmrk and EGFR signaling utilize STAT5 to regulate cell proliferation, and Xmrk may signal through PI3K and FasR to modulate apoptosis. At the same time, both activate the Ras/Raf/MEK/MAPK pathway to regulate cell proliferation and E-cadherin signaling. Xmrk models of melanoma have shown that inhibitors of PI3K and MEK have an anti-cancer effect, and in HCC, that the steroidal drug, adrenosterone, can prevent metastasis and recover E-cadherin expression, suggesting that fish Xmrk models can exploit similarities with EGFR signal transduction to identify and study new chemotherapeutic drugs.

摘要

在多个鱼类物种(如绿色剑尾鱼和黄斑蓝皮鱼杂交鱼、斑马鱼和青鳉)中进行的研究已经确定了受体酪氨酸激酶 Xmrk 的致癌作用,Xmrk 是一种与人表皮生长因子受体 (EGFR) 密切相关的基因产物,与多种病理状况有关,包括癌症。对黑色素瘤中 Xmrk 和 EGFR 信号转导的比较分析表明,两者都利用 STAT5 信号来调节细胞凋亡和细胞增殖,利用 PI3K 来调节细胞凋亡,利用 FAK 来控制细胞迁移,利用 Ras/Raf/MEK/MAPK 通路来调节细胞存活、增殖和分化。此外,Xmrk 和 EGFR 还可能调节黑色素瘤中类似的趋化因子、细胞外基质、氧化应激和 microRNA 信号通路。在肝细胞癌 (HCC) 中,Xmrk 和 EGFR 信号通过 STAT5 调节细胞增殖,Xmrk 可能通过 PI3K 和 FasR 信号调节细胞凋亡。同时,两者都激活 Ras/Raf/MEK/MAPK 通路来调节细胞增殖和 E-钙粘蛋白信号。黑色素瘤的 Xmrk 模型表明,PI3K 和 MEK 的抑制剂具有抗癌作用,而在 HCC 中,甾体药物肾上腺酮可以预防转移并恢复 E-钙粘蛋白的表达,这表明鱼类 Xmrk 模型可以利用与 EGFR 信号转导的相似性来识别和研究新的化疗药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/99dc/8150686/c116000e378a/cells-10-01132-g001.jpg

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