Simultaneous induction and blockade of autophagy by a single agent.

Besides cell death, autophagy and cell senescence are the main outcomes of anticancer treatment. We demonstrate that tacrine-melatonin heterodimer C10, a potent anti-Alzheimer's disease drug, has an antiproliferative effect on MCF-7 breast cancer cells. The main cell response to a 24 h-treatment with C10 was autophagy enhancement accompanied by inhibition of mTOR and AKT pathways. Significantly increased autophagy markers, such as LC3B- and ATG16L-positive vesicles, confirmed autophagy induction by C10. However, analysis of autophagic flux using mCherry-GFP-LC3B construct revealed inhibition of autophagy by C10 at the late-stage. Moreover, electron microscopy and analysis of colocalization of LC3B and LAMP-1 proteins provided evidence of autophagosome-lysosome fusion with concomitant inhibition of autolysosomal degradation function. After transient treatment with IC50 dose of C10 followed by cell culture without the drug, 20% of MCF-7 cells displayed markers of senescence. On the other hand, permanent cell treatment with C10 resulted in massive cell death on the 5th or 6th day. Recently, an approach whereby autophagy is induced by one compound and simultaneously blocked by the use of another one has been proposed as a novel anticancer strategy. We demonstrate that the same effect may be achieved using a single agent, C10. Our findings offer a new, promising strategy for anticancer treatment.

Curcumin induces senescence of primary human cells building the vasculature in a DNA damage and ATM-independent manner.

Curcumin is considered not only as a supplement of the diet but also as a drug in many types of diseases and even as a potential anti-aging compound. It can reduce inflammation that increases with age and accompanies almost all age-related diseases. It has been suggested that curcumin can play a beneficial role in the cardiovascular system. However, there are also data showing that curcumin can induce senescence in cancer cells, which is a beneficial effect in cancer therapy but an undesirable one in the case of normal cells. It is believed that cellular senescence accompanies age-related changes in the cardiovascular system. The aim of this study was to check if curcumin, in a certain range of concentrations, can induce senescence in cells building the vasculature. We have found that human vascular smooth muscle and endothelial cells derived from aorta are very sensitive to curcumin treatment and can senesce upon treatment with cytostatic doses. We observed characteristic senescence markers but the number of DNA damage foci decreased. Surprisingly, in vascular smooth muscle cell (VSMC) activation of DNA damage response pathway downstream of ataxia-telangiectasia mutated (ATM) was observed. ATM silencing and the supplementation of antioxidants, N-acetyl-L-cysteine (NAC) or trolox, did not reduce the number of senescent cells. Thus, we have shown that curcumin can induce senescence of cells building the vasculature, which is DNA damage and ATM independent and is not induced by increased reactive oxygen species (ROS) level. We postulate that an increase in the bioavailability of curcumin should be introduced very carefully considering senescence induction as a side effect.

[Natural compounds--modulators of senescence and cell death]. / Zwiqzki pochodzenia naturalnego modulujace starzenie i smierc komórek.

For hundreds of years natural compounds have been used in herbal medicine. They have been known for their antibacterial, antifungal, anticancer activities as well as for enhancing wound healing and improving immunity. Recently growing interest in natural compounds has been observed, due to their ability to modulate cellular senescence. Particularly interesting are these compounds that can induce tumor senescence, delay senescence of normal cells or reverse changes associated with senescence - acting as "rejuvenation" agents. It has been shown that some of the natural compounds can both promote senescence of tumor cells as well as prevent it in normal cells. Thus, they can be useful in therapy of age-related diseases. Natural compounds can regulate nutrient and energy sensing signaling pathways that are involved in senescence. They can also influence the synthesis of reactive oxygen species, secretion of cytokines, telomere shortening or epigenetic changes of DNA. Natural agents often act in a pleiotropic manner. They can modulate cellular senescence in many ways e.g. by direct neutralization of free radicals and affecting other regulatory signaling pathways. Furthermore natural compounds, commonly used for years e.g. as spices, usually don't have any side effects. Therefore their use as dietary supplements or in long term therapy appears to be relatively safe.