Right here, we devised a new strategy for eradicating malignancy stem cells (CSCs), via a synthetic-metabolic approach, including two FDA-approved antibiotics and a dietary vitamin supplement. strong inhibitory effects of this DAV triple combination therapy on mitochondrial oxygen usage and ATP production were directly validated using metabolic flux analysis. Consequently, the induction of mitochondrial biogenesis due to mild oxidative stress, coupled with inhibition of mitochondrial protein translation, may be a new encouraging therapeutic anti-cancer strategy. Consistent CCK2R Ligand-Linker Conjugates 1 with these assertions, Vitamin C is known to become highly concentrated within mitochondria, by a specific transporter, namely SVCT2, inside a sodium-coupled way. Also, the concentrations of antibiotics utilized right here represent sub-antimicrobial degrees of Azithromycin and Doxycycline, thus preventing the potential complications connected with antibiotic level of resistance. Finally, we also discuss possible implications for improving health-span and life-span, as Azithromycin is an anti-aging drug that behaves like a senolytic, which selectively kills and removes senescent fibroblasts. and evidence helps the potential inhibitory effects of Doxycycline on cancer growth through inhibition of CSC propagation [1C5]. More specifically, we demonstrated that Doxycycline inhibits CSC propagation, as assessed using the 3D mammosphere assay, with an IC-50 between 2-to-10 M, specifically in MCF7 cells, an ER(+) human breast cancer cell line [1,2]. Importantly, quantitatively similar results were obtained with several other human breast cancer cell lines, such as T47D [ER(+)] and MDA-MB-231 (triple-negative). Recently, Antibiotic for Breast Cancer (ABC) trial was conducted at The University of Pisa Hospital . The ABC trial aimed to assess the anti-proliferative and anti-CSC mechanistic actions of Doxycycline in early breast cancer patients . The primary endpoint of the ABC trial was to determine whether short-term (2 weeks) pre-operative treatment with oral Doxycycline of stage I-to-III early breast cancer patients resulted in inhibition of tumor proliferation markers, as determined by a reduction in tumor Ki67 from baseline (pre-treatment) to post-treatment, at the time of surgical excision . Secondary endpoints were used to determine if pre-operative treatment with CCK2R Ligand-Linker Conjugates 1 Doxycycline in the same breast cancer patients resulted in inhibition of CSC propagation and a reduction of mitochondrial markers. A pilot study of the ABC trial demonstrated that Doxycycline treatment successfully decreased the expression of CSC markers in breast cancer tumor samples. Post-doxycycline tumor samples demonstrated a statistically significant 40% decrease in the stemness marker CD44, when compared to pre-Doxycycline tumor samples . CD44 levels were reduced between 17.65% and 66.67%, in 8 out of 9 patients treated with Doxycycline . In contrast, only one patient showed a rise in CD44, by 15%. This represents a nearly 90% positive response rate. Similar results were also obtained with ALDH1 , another marker of stemness, especially in HER2(+) patients. In contrast, markers CD253 of mitochondria, proliferation, apoptosis and neo-angiogenesis, were all similar between the two groups. These results suggest that Doxycycline can selectively eradicate CSCs in breast cancer patients . Given these promising results in the ABC pilot study, here we aimed to potentiate the efficacy of Doxycycline further, for patient advantage. Our preliminary outcomes indicate how the inhibitory ramifications CCK2R Ligand-Linker Conjugates 1 of Doxycycline on CSC propagation could be additional potentiated, by using a mixture therapy technique, with two extra pharmacological agents, specifically i) Azithromycin and ii) Supplement C. Azithromycin inhibits the top mitochondrial ribosome, as an off-target side-effect. Supplement C functions as a CCK2R Ligand-Linker Conjugates 1 gentle pro-oxidant, that may produce free of charge radicals and, as a result, induces mitochondrial biogenesis. This mixture therapy was made to stimulate mitochondrial biogenesis, while inhibiting mitochondrial proteins translation concurrently, resulting in practical ATP depletion. This happens because inhibition of mitochondrial proteins translation efficiently blocks the creation of protein encoded by mitochondrial DNA (mt-DNA), that are necessary for OXPHOS definitely, thereby creating.