Truu 2017 MiP2017
We have analyzed quantitatively the mitochondrial respiration in human post-operational tissue samples in colorectal cancer (HCC), normal colon tissues, colon polyps and in breast cancer (HBC). We also included MDA-MB 231 and MCF-7 cultures. In this work the technique of permeabilized fibers is used, which takes into account the complex structural and functional organization of tissue and its importance for metabolic regulation. The flux was measured as the rate of oxygen consumption, using High-Resolution FluoRespiromety (Oroboros Instruments, Austria). Mitomed medium was used for measurement, containing 5mM glutamate, 2mM malate and 10mM of succinate as substrates.
Our results show that HCC is not fully glycolytic tumor and OXPHOS system might be the main source of ATP. Kinetic parameters displayed remarkable differences between cell cultures and clinical HBC samples. Comparing healthy colon, HCC tissue and colon polyps, we found that colon polyps (52,5 ± 12,7; µM ± SEM) show similar Km values to healthy mucosal colon tissue (42 ± 14; µM ± SEM) rather than HCC (69 ± 10; µM ± SEM). We identified that the development of colon polyps results in reduced VGlut/VSucc ratio which indicates relative suppression of complex I dependent respiration, which is the hallmark of multiple mitochondrial diseases and is generally considered to be an essential property of some cancers. However, relative Complex I functional deficiency was characteristic for HCC, but not for HBC. HCC was characterized with higher mitochondrial biogenesis compared with normal colon tissue.
Further research is in progress to generate a full cancer development model consisting of cell cultures, clinical polyps and malignant versus healthy tissue samples.
Labels: MiParea: Respiration, mt-Biogenesis;mt-density, Patients Pathology: Cancer
Preparation: Permeabilized tissue
Pathway: N, NS HRR: Oxygraph-2k
- Truu L(1), Koit A(1), Chekulayev V(1), Tepp K(1), Puurand M(1), Ounpuu L(1), Klepinin A(1), Shevchuk I(1), Kaambre T(1,2)
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