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A novel drug therapeutic treatment: Hydrogen uncaging using flash photolysis for fast and focal intracellular acidification as a cancer therapeutic system.

机译:一种新颖的药物治疗方法:使用快速光解氢解开氢,以快速而集中地将细胞内酸化,作为一种癌症治疗系统。

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摘要

Current therapies for many types of cancers involve the disruption of the cancer cells' ability to alter intracellular pH (pH i). Virtually all mammalian cells, including cancerous cells, ubiquitously express the transmembrane sodium-hydrogen exchanger (NHE1), which is used to regulate pHi, salt concentrations and cell volume. Cancer cells use NHE1 to their advantage by upregulating the expression of the NHE1 protein and continually activating NHE1 to achieve cytosolic alkalization as well as extracellular acidification for increased local vascularization. Many chemotherapeutic approaches to cancer treatment involve the use of proton pump inhibitors (PPI's) to block NHE1 in order to cause a decrease in pHi and disrupt cell functions and tumor progression. However, PPI's are systemically delivered and often cause devastating side effects to normal cells. Our lab developed a novel technique using the photolytic compound 2-nitrobenzaldehyde (NBA) to induce fast and focal intracellular acidification by releasing hydrogen ions in the presence of ultraviolet (UV) light in healthy rat pheochromocytoma (PC12) cells and MCF-7 breast cancer cells. The cancer cells were also treated with NBA-conjugated upconversion nanoparticles to absorb near infrared light and emit UV light for non-invasive remote activation of NBA. This hydrogen uncaging technique has shown exceedingly high cell death through the activation of a previously undiscovered positive feedback loop seen in in MCF-7 cancer cells but not in healthy PC12 cells. The use of NBA and NBA-conjugated nanoparticles also showed minimal cytotoxic effects in the absence of UV activation. These results support our hypothesis that focal intracellular acidification would be an excellent candidate for future cancer therapeutics.
机译:当前针对多种类型癌症的疗法涉及破坏癌细胞改变细胞内pH(pH i)的能力。几乎所有的哺乳动物细胞,包括癌细胞,都普遍表达跨膜钠氢交换剂(NHE1),用于调节pHi,盐浓度和细胞体积。癌细胞通过上调NHE1蛋白的表达并持续激活NHE1来实现胞浆碱化以及细胞外酸化以增加局部血管形成,从而发挥NHE1的优势。许多用于癌症治疗的化学疗法涉及使用质子泵抑制剂(PPI's)阻断NHE1,以引起pHi降低并破坏细胞功能和肿瘤进展。但是,PPI是全身性递送的,通常会对正常细胞造成破坏性的副作用。我们的实验室开发了一种新技术,利用光解化合物2-硝基苯甲醛(NBA)在健康大鼠嗜铬细胞瘤(PC12)细胞和MCF-7乳腺癌中,在存在紫外线(UV)的情况下通过释放氢离子来诱导快速而集中的细胞内酸化细胞。癌细胞还经过NBA共轭上转换纳米粒子处理,以吸收近红外光并发射紫外线,从而实现NBA的无创远程激活。通过激活先前未发现的正反馈回路,这种氢解开氢技术已显示出极高的细胞死亡,这种回路在MCF-7癌细胞中可见,而在健康的PC12细胞中却没有。在没有紫外线激活的情况下,使用NBA和结合NBA的纳米颗粒也显示出最小的细胞毒性作用。这些结果支持我们的假设,即局灶性细胞内酸化将是未来癌症治疗的极佳候选者。

著录项

  • 作者

    O'Grady, Brian.;

  • 作者单位

    The University of Texas at San Antonio.;

  • 授予单位 The University of Texas at San Antonio.;
  • 学科 Cellular biology.;Biology.;Oncology.
  • 学位 M.S.
  • 年度 2014
  • 页码 72 p.
  • 总页数 72
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

  • 入库时间 2022-08-17 11:40:36

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