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A nonmainstream approach against cancer

机译:对癌症的非玛瑙方法

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The discovery of antibiotics as specific and effective drugs against infectious agents has generated the belief that the famous Paul Erlich theory on magic bullet should be applied to cancer as well. However, after around 60 years of failures in finding a magic bullet against cancer, a question appears mandatory: does the magic bullet against cancer really exist? In trying to understand more on the issue, we propose three discoveries are coming from a nonmainstream approach against cancer. Tumor is acidic, and tumor acidity impairs drugs entering within tumor cells and isolates tumors from the rest of the body. Proton pumps are key in allowing tumor cells to live in the acidic microenvironment. A class of antiacidic drugs, proton pump inhibitors (PPIs), were shown to have a potent anti-tumor effect, through inhibition of proton pumps in tumor cells. PPIs are indeed prodrugs needing acidity to be activated into the active molecule. So they use protonation by H+ as an activating mechanism, while the vast majority of drugs are totally neutralized by protonation. An anti-tumor therapy based on PPI showed to be effective both in vitro and in vivo. Differently from normal cells, cancer cells meet their energy needs in great part by fermentation, and it appears conceivable that hypoxia and low nutrient transform tumor cells into fermenting anaerobes. This suggests that cancer cells are more similar to unicellular organisms, aimed at surviving in a continuous fighting, rather than cooperating, with other cells, as it occurs in the normal homeostasis of our body. We have shown that cancer cells take their fuel by "cannibalizing'' other cells, either dead or alive, especially when starved and in acidic condition. This finding led to the discovery of a new oncogene TM9SF4 that human malignant cell shares with amoebas. The evidence is accumulating that almost all the cells release extracellular vehicles (EVs), from micro- to nanosize, which shuttle a variety of molecules. Tumor cells, particularly when stressed in their hostile microenvironment, release high levels of EVs, able to interact with target cells in various ways, within an organ or at a distance. They may represent both valuable tumor biomarker and shuttles for drugs with anti-tumor properties. This article wants to burst a real change in future anti-cancer strategies, based on the idea that tumors are much more common features than specific molecular targets.
机译:作为特定和有效的针对传染性药物的抗生素发现的发现已经产生了魔术子弹的着名保罗尔·埃莱希理论,也应适用于癌症。然而,在大约60年的失败后寻找魔术子弹患有针对癌症的魔术子弹,一个问题似乎强制性:魔术子弹对抗癌症真的存在吗?在试图了解更多问题时,我们提出了三个发现来自非母目对抗癌症的方法。肿瘤是酸性的,肿瘤酸度损害在肿瘤细胞内进入的药物,并将肿瘤与身体的其余部分分离出来。质子泵是允许肿瘤细胞生活在酸性微环境中的关键。通过抑制肿瘤细胞中的质子泵,显示了一类抗亚替视药,质子泵抑制剂(PPI)具有效率的抗肿瘤作用。 PPI是需要酸度被激活到活性分子中的前药。因此,它们使用H +作为激活机制的质子化,而绝大多数药物被质子化完全中和。基于PPI的抗肿瘤治疗显示在体外和体内有效。与正常细胞不同,癌细胞以发酵在很大程度上满足其能量需求,并且缺氧和低营养素将肿瘤细胞转化为发酵厌氧菌。这表明癌细胞更类似于单细胞生物,旨在在连续战斗中存活,而不是与其他细胞一起存活,因为它发生在我们身体的正常稳态中。我们已经表明,癌细胞通过“蚕食”其他细胞,尤其是在饥饿和酸性条件下的情况下“蚕食”其他细胞来燃料。这种发现导致了一种新的癌基因TM9SF4,人类恶性细胞与AmoEbas股份。该证据积累了几乎所有细胞释放细胞外载体(EVS),从微量到纳米尺寸,穿梭于各种分子。肿瘤细胞,特别是当在其敌对微环境中胁迫时,释放高水平的EV,能够与目标相互作用细胞以各种方式,在器官内或远处。它们可以代表具有抗肿瘤性质的药物的有价值的肿瘤生物标志物和梭子。本文基于这一想法,本文希望在未来的抗癌策略中突发真正的变化肿瘤比特定分子靶标更常见。

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