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首页> 外文期刊>Expert opinion on therapeutic targets >Lemur tyrosine kinase-3 (LMTK3) as a target in oestrogen positive breast cancer.
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Lemur tyrosine kinase-3 (LMTK3) as a target in oestrogen positive breast cancer.

机译:狐猴酪氨酸激酶3(LMTK3)作为雌激素阳性乳腺癌的靶标。

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摘要

Oestrogen receptor positive (ER~+) breast cancers are susceptible to endocrine treatments, such as tamoxifen. However, resistance is a major problem when treating breast cancer with these agents. ERalpha phosphorylation is implicated in this resistance to tamoxifen, and kinases are the enzymes that catalyse phosphorylation. A kinome search in human breast cancer cells identified lemur tyrosine kinase 3 (LMTK3). In primary breast cancer samples, high nuclear LMTK3 expression was associated with a shorter disease-free survival time. In tamoxifen-resistant cell lines, the addition of LMTK3 siRNA, increased the inhibitory effect of tamoxifen. In nude mice, with established human MCF-7 breast cancer tumours, LMTK3 siRNA decreased tumour growth. In conclusion, LMKT3 is a possible target and marker of breast cancer.
机译:雌激素受体阳性(ER〜+)乳腺癌易受内分泌治疗,例如他莫昔芬。但是,当用这些药物治疗乳腺癌时,耐药性是主要问题。 ERalpha磷酸化与对他莫昔芬的抗性有关,激酶是催化磷酸化的酶。在人乳腺癌细胞中进行的基因组搜索确定了狐猴酪氨酸激酶3(LMTK3)。在原发性乳腺癌样本中,高核LMTK3表达与较短的无病生存时间相关。在他莫昔芬耐药细胞系中,LMTK3 siRNA的添加增加了他莫昔芬的抑制作用。在具有确定的人MCF-7乳腺癌肿瘤的裸鼠中,LMTK3 siRNA降低了肿瘤的生长。总之,LMKT3是乳腺癌的可能靶标和标志物。

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