曲妥珠单抗
张力素
PTEN公司
癌症研究
乳腺癌
医学
蛋白激酶B
癌细胞
细胞凋亡
癌症
细胞生长
药理学
内科学
肿瘤科
化学
PI3K/AKT/mTOR通路
生物化学
作者
Akram Sadeghirizi,Razieh Yazdanparast,Safiyeh Aghazadeh
出处
期刊:Tumor Biology
[SAGE]
日期:2015-12-10
卷期号:37 (5): 6737-6747
被引量:13
标识
DOI:10.1007/s13277-015-4424-9
摘要
Trastuzumab is by far the drug of choice for treatment of human epidermal growth factor receptor 2 (Her2) overexpressing breast cancer patients. However, frequently, the therapy remains ineffective due to the induced drug resistance. In spite of various reported mechanisms, we hypothesize that the acquired resistance to trastuzumab might be attributed to the failure of the drug to activate phosphatase and tensin homolog (PTEN) mainly due to the high level of reduced thioredoxin-1 protein among the resistant cells. In the present study, the effect(s) of PX-12, a Trx-1 inhibitor, was examined on proliferation of breast cancer cells which are unresponsive to trastuzumab. Treatment of the cells with PX-12 (5 μM) and trastuzumab (10 μg/ml) reduced cells viabilities, p-Akt, and Bcl2 levels while increasing the levels of reactive oxygen species (ROS) and p-JNK with consequent higher levels of G1 arrest and apoptosis among the resistant cells compared to parental trastuzumab sensitive cells. The most significant observation was that PX-12/trastuzumab co-treatment enhanced the cell membrane localization of PTEN which is believed to be the active biological form of the signal. Our data confirmed that Trx-1 inhibition is required for chemosensitization of resistant breast cancer cells to anti-Her2 therapy, and this approach might offer an alternative clinical strategy for preventing acquired resistance.
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