Maedo 2014 Abstract IOC 2014-04 Schroecken

From Bioblast
Maedo (2014) The regulation of mitochondrial respiration in human colorectal cancer cells in situ: the possible role of beta-tubulins Mitochondr Physiol Network 19.02.

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Maedo K, KaldmaA, Planken A, Klepinin A, Chekulayev V, Varikmaa M, Tepp K, Chevchuk I, Kaambre T (2014)

Event: IOC 2014-04 Schroecken

For decades it has been known that cancer cells establish a specific metabolic profile, characterized as aerobic fermentation or the Warburg effect. Now it has become more clear that at least some cancers exhibit increased oxydative phosphorylation (OXPHOS). We have analyzed human post-operative tissue samples from colorectal adenocarcinomas and compared it to adjacent normal colon tissue samples. The preliminary results indicate that the colorectal adenocarcinoma is not a pure glycolytic tumor and the OXPHOS system may be the main provider of ATP in these cells. The apparent Km for ADP and Vmax values are calculated for the characterization of the affinity of mitochondria for exogenous ADP: normal colon tissue displayed very low affinity for ADP (Km β‰ˆ 250Β΅M) instead of tumor tissue, where the affinity was significantly higher (Km β‰ˆ 120Β΅M). At the same time there was 1,75 times higher maximal respiration rate in tumor samples compared to normal, suggesting cancer`s enhanced respiration capacity. Changes in the value of the apparent Km for ADP has been previously associated with the binding of cytoskeletal tubulin to voltage dependent anion channel (VDAC) in the mitochondrial outer membrane. In cardiomyocytes VDAC is probably regulated by tubulin Ξ²II isoform. To clarify the role of tubulins in cancer and normal colon tissue samples we examined tubulin Ξ²I, Ξ²II, Ξ²III and Ξ²IV mRNA and protein expression profiles. Our results show that tubulin Ξ²II expression levels are similar in both samples, but there is an increase in tumour`s tubulin Ξ²III level. To conclude, in colorectal cancer other mechanisms are probably involved in the permeability of VDAC for ADP.


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