维甲酸-聚乙二醇-硫醇金纳米颗粒偶联物治疗宫颈癌的前景看好。

IF 0.2 Q4 MEDICINE, RESEARCH & EXPERIMENTAL International journal of clinical and experimental medicine Pub Date : 2015-07-15 eCollection Date: 2015-01-01
Li Ye, Qian Song
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引用次数: 0

摘要

研究了合成的维甲酸-聚乙二醇-硫醇金纳米颗粒偶联物对宫颈癌细胞的作用。宫颈癌是发展中国家育龄妇女死亡的主要原因。与维甲酸相比,纳米粒子缀合物对宫颈癌具有更好的活性。观察到金纳米颗粒偶联物选择性递送至雌激素受体阳性宫颈癌细胞,其药物效力增强6倍。发现金纳米颗粒的转移受雌激素配体和受体的支配。维甲酸纳米颗粒缀合物似乎被存在于质膜中的雌激素受体α选择性地摄取和保留。因此,纳米颗粒连接显著提高了RA-PEG-SH的IC50值。用ra - peg - sh - aunps处理的细胞在孵育后12和24小时表现出生长抑制。RA- peg - sh - aunps在12 h和24 h的IC50分别为3 μM和1 μM。因此,使用RA纳米颗粒偶联物可能是宫颈癌治疗的更好策略。
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Promising potency of retinoic acid-poly(ethylene glycol)-thiol gold nanoparticle conjugates for cervical cancer treatment.

We investigated the effect of synthesized retinoic acid-poly(ethylene glycol)-thiol gold nanoparticle conjugates on cervical carcinoma cells. Cervical cancer is the major cause of deaths for the women of reproductive age in the developing countries. Compared to retinoic acid, the nanoparticle conjugates exhibited better activity against cervical carcinoma. Selective delivery of gold nanoparticle conjugates to estrogen receptor positive cervical cancer cells with 6-fold enhanced drug potency was observed. Transfer of gold nanoparticles was found to be dominated by estrogen ligand and receptor. It appeared that retinoic acid nanoparticle conjugates were selectively taken and retained by the estrogen receptor alpha present in the plasma membrane. Thus IC50 values for RA-PEG-SH were significantly improvedon nanoparticle ligation. Cells on treatment with RA-PEG-SH-AuNPsshowed growth inhibition at 12 and 24 h after incubation. The IC50 for RA in RA-PEG-SH-AuNPs after 12 and 24 h were 3 and 1 μM, respectively. Thus, the use of RA nanoparticle conjugates can be a better strategy for cervical carcinoma treatment.

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