SHP2在乳腺癌侵袭转移中的作用

Qinanqian Chen, Ying Zheng, Bin Zhang, Xuchen Cao
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引用次数: 0

摘要

Src同源2结构域磷酸酶(SHP2)是一种跨膜蛋白酪氨酸磷酸酶,由原癌基因PTPN11编码。SHP2通过调节细胞内蛋白酪氨酸磷酸化水平,在细胞信号转导通路和细胞活动中发挥重要作用。SHP2的激活状态与乳腺癌的激素水平调控、肿瘤的侵袭转移状态、肿瘤干细胞的发生进展以及Ras/ERK、PI3K/Akt/mTOR等信号通路密切相关。基因敲除或基因沉默表达有助于抑制肿瘤生长,不可逆地阻碍肿瘤重新获得干细胞的能力,扰乱乳腺癌侵袭转移的信号通路。最近的研究表明,SHP2可能有助于将抗癌药物提高到更高的水平。本文就SHP2与乳腺癌侵袭转移关系的研究进展作一综述。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Role of SHP2 in invasion and metastasis of breast cancer
Src homology 2 domain-containing phosphatase (SHP2), which is encoded by proto-oncogene PTPN11, is one of the transmembrane protein-tyrosine phosphatases. SHP2 has an important function in signal transduction pathways and activities of cells through the regulation of tyrosine phosphorylation level of intracellular proteins. The status of SHP2 activation is closely connected with the regulation of hormone levels, state of invasion and metastasis of tumor, development and progression of tumor stem cells of breast cancer, as well as signal pathways including Ras/ERK and PI3K/Akt/mTOR. Gene knockout or gene silencing expression helps inhibit tumor growth, irreversibly hindering the ability of the tumor to regain stem cells and disturb the signal pathways of the invasion and metastasis of breast cancer. Recent studies have shown that SHP2 may help in bringing anticancer drugs to a higher level. This article concentrates on the research progress in relationship of SHP2 with invasion and metastasis of breast cancer.
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