Posted on 02/08/2015 4:37:54 PM PST by 2ndDivisionVet
Abstract
Here, we propose a new strategy for the treatment of early cancerous lesions and advanced metastatic disease, via the selective targeting of cancer stem cells (CSCs), a.k.a., tumor-initiating cells (TICs). We searched for a global phenotypic characteristic that was highly conserved among cancer stem cells, across multiple tumor types, to provide a mutation-independent approach to cancer therapy. This would allow us to target cancer stem cells, effectively treating cancer as a single disease of stemness, independently of the tumor tissue type. Using this approach, we identified a conserved phenotypic weak point a strict dependence on mitochondrial biogenesis for the clonal expansion and survival of cancer stem cells. Interestingly, several classes of FDA-approved antibiotics inhibit mitochondrial biogenesis as a known side-effect, which could be harnessed instead as a therapeutic effect. Based on this analysis, we now show that 4-to-5 different classes of FDA-approved drugs can be used to eradicate cancer stem cells, in 12 different cancer cell lines, across 8 different tumor types (breast, DCIS, ovarian, prostate, lung, pancreatic, melanoma, and glioblastoma (brain)). These five classes of mitochondrially-targeted antibiotics include: the erythromycins, the tetracyclines, the glycylcyclines, an anti-parasitic drug, and chloramphenicol. Functional data are presented for one antibiotic in each drug class: azithromycin, doxycycline, tigecycline, pyrvinium pamoate, as well as chloramphenicol, as proof-of-concept. Importantly, many of these drugs are non-toxic for normal cells, likely reducing the side effects of anti-cancer therapy....
(Excerpt) Read more at impactjournals.com ...
I fb mailed my friend who will get the info from her dad later today. I will post when I hear more.
Thanks Civ
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Thanks, Tired of Taxes. Good study. Hopeful stuff.
It is hopeful, isn’t it? God bless, Xzins.
Thanks, Chickensoup. That will be great!
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