研究人员找到杀死癌细胞的精确方法
Researchers Find Precise Way To Kill Cancer Cells

原始链接: https://www.zerohedge.com/medical/researchers-find-precise-way-kill-cancer-cells

伊利诺伊大学厄巴纳-香槟分校的科学家开发了一种利用光而不是传统化学疗法来对抗癌细胞的新方法。 这种技术被称为光遗传学,将高度针对性的光束聚焦到单个癌细胞上,启动它们的自我毁灭,同时保持附近的健康细胞不受影响。 同时,这个过程会触发免疫系统,促使白细胞到达并增强身体对未来威胁的防御能力。 研究人员通过将植物的光响应基因整合到肠道细胞培养物中,并将其与负责调节程序性细胞死亡或坏死性凋亡的基因偶联,实现了这一突破。 研究生兼主要作者 Teak-Jung Oh 解释说,当暴露在光线下时,RIPK3 蛋白会聚集在一起,引发连锁反应,导致坏死性凋亡。 了解这种机制不仅可能有助于治疗癌症,还可能有助于治疗与坏死性凋亡相关的其他疾病,例如神经退行性疾病和炎症性肠病。 他们的研究结果发表在《分子生物学杂志》上。

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原文

Authored by Huey Freeman via The Epoch Times (emphasis ours),

Cancer treatments that aim to destroy deadly cells often cause damage and pain as they wreak havoc on neighboring cells and tissues. However, scientists have discovered a new method of targeting harmful cells using light for precise destruction, according to a recent study.

“Usually treatments for cancer use pharmacological induction to kill the cells, but those chemicals tend to diffuse throughout the tissues and it’s hard to contain to a precise location,” said University of Illinois Urbana-Champaign biochemistry professor and study leader Kai Zhang in a press release. “You get a lot of unwanted effects.”

Cancer cells 3D illustration. (Jezper/Shutterstock)

The researchers deploy optogenetics, an approach that uses optical systems to control cell functions, to focus a light beam on a target smaller than one cell.

That is how we can use light to very precisely target a cell and turn on its death pathway,” Mr. Zhang said in the press release.

In addition to killing the cancer cell, another intended outcome is to trigger the immune system to respond to the light. Mr. Zhang said that the ruptured cells release cytokines, a type of small protein, attracting white blood cells that help the immune system fight infection. By killing cancer cells, the researchers hope to train T-cell white blood cells to recognize and attack the cancer, Mr. Zhang said.

The researchers made the cells respond to light by borrowing a light-activated gene from plants and inserting it into intestine cell cultures. They then attached those genes to the genes for a protein, RIPK3, that regulates necroptosis, a form of cell death caused by various stimuli.

Teak-Jung Oh, a graduate student and the paper’s first author, said the light activation process causes the RIPK3 proteins to cluster together, mimicking the natural death pathway.

Understanding the cell signaling pathway for necroptosis is especially important because it has been known to be involved with diseases like neurodegenerative disease and inflammatory bowel disease,” said Mr. Oh. “Knowing how necroptosis affects progression in these diseases is important. And if you don’t know the molecular mechanisms, you don’t really know what to target to slow the progression.”

The study was published in the July issue of the Journal of Molecular Biology.

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