Roles of circadian clocks in cancer pathogenesis and treatment

Circadian clocks are ubiquitous timing mechanisms that generate approximately 24-h rhythms in cellular and bodily functions across nearly all living species. These internal clock systems enable living organisms to anticipate and respond to daily changes in their environment in a timely manner, optimizing temporal physiology and behaviors. Dysregulation of circadian rhythms by genetic and environmental risk factors increases susceptibility to multiple diseases, particularly cancers. A growing number of studies have revealed dynamic crosstalk between circadian clocks and cancer pathways, providing mechanistic insights into the therapeutic utility of circadian rhythms in cancer treatment. This review will discuss the roles of circadian rhythms in cancer pathogenesis, highlighting the recent advances in chronotherapeutic approaches for improved cancer treatment.Subject terms: Circadian rhythms, Targeted therapies     

Circadian variations in biologically closed electrochemical circuits in Aloe vera and Mimosa pudica

The circadian clock regulates a wide range of electrophysiological and developmental processes in plants. This paper presents, for the first time, the direct influence of a circadian clock on biologically closed electrochemical circuits in vivo. Here we show circadian variation of the plant responses to electrical stimulation. The biologically closed electrochemical circuits in the leaves of Aloe vera and Mimosa pudica, which regulate their physiology, were analyzed using the charge stimulation method. The electrostimulation was provided with different timing and different voltages. Resistance between Ag/AgCl electrodes in the leaf of Aloe vera was higher during the day than at night. Discharge of the capacitor in Aloe vera at night was faster than during the day. Discharge of the capacitor in a pulvinus of Mimosa pudica was faster during the day. The biologically closed electrical circuits with voltage gated ion channels in Mimosa pudica are also activated the next day, even in the darkness. These results show that the circadian clock can be maintained endogenously and has electrochemical oscillators, which can activate ion channels in biologically closed electrochemical circuits. We present the equivalent electrical circuits in both plants and their circadian variation to explain the experimental data.     

Biological clocks: mechanisms and developments.

Almost all organisms ranging from unicellular protists to mammals were found to show biological rhythms. Many workers have performed various kinds of experiment to understand the mechanism as well as to find the origin of the clock responsible for these rhythms. However, there is no doubt about the existence of a biologically controlled clock in almost all organisms; yet its origin and mechanism still remain a mystery. Many theories have been put forward to explain the mechanism of these biological clocks and it seems that the cell membrane may play a key role. The existence of a very high electric field of the order of 10(5) V cm-1 across the cell membrane may have some role in the mechanism of the biological clock. Of all the factors which have the effects on biological rhythms, light and temperature are found to be the most common. Also, the study of these biological clocks can help to solve the sleeping problems of international travellers and shift workers as well as to improve diagnosis, cure and prevention from diseases.     

Sleep,circadian rhythms,and the pathogenesis of Alzheimer Disease

Disturbances in the sleep–wake cycle and circadian rhythms are common symptoms of Alzheimer Disease (AD), and they have generally been considered as late consequences of the neurodegenerative processes. Recent evidence demonstrates that sleep–wake and circadian disruption often occur early in the course of the disease and may even precede the development of cognitive symptoms. Furthermore, the sleep–wake cycle appears to regulate levels of the pathogenic amyloid-beta peptide in the brain, and manipulating sleep can influence AD-related pathology in mouse models via multiple mechanisms. Finally, the circadian clock system, which controls the sleep–wake cycle and other diurnal oscillations in mice and humans, may also have a role in the neurodegenerative process. In this review, we examine the current literature related to the mechanisms by which sleep and circadian rhythms might impact AD pathogenesis, and we discuss potential therapeutic strategies targeting these systems for the prevention of AD.     

Neuroanatomical approaches to the study of insect photoperiodism

The anatomical locations of three components of insect photoperiodism--the photoperiodic photoreceptor, photoperiodic clock and hormonal effector--are summarized and compared between species. Among photoperiodic photoreceptors, either the retinal or extraretinal types or both are operative, and there is no general relationship between phylogeny and photoreceptor type. The photoperiodic clock comprises time measurement and counter systems. Currently, it is generally accepted that circadian oscillators are involved in the photoperiodic clock. Several recent studies have raised the possibility that timeless, a circadian clock gene, plays a role in the photoperiodic clock in flies. The dorsal protocerebrum has been identified as an important region regulating the endocrine system for adult, pupal and embryonic diapause controlled by photoperiod. In the blow fly Protophormia terraenovae, neural connections between circadian clock neurons and indispensable neurons in the pars lateralis for diapause induction in the dorsal protocerebrum have been demonstrated. This neural network may provide the access needed to investigate the neural components of the photoperiodic clock.     

Crayfish Procambarus clarkii retina and nervous system exhibit antioxidant circadian rhythms coupled with metabolic and luminous daily cycles

Based on previous work in which we proposed midgut as a putative peripheral oscillator responsible for circadian reduced glutathione (GSH) crayfish status, herein we investigated the retina and optic lobe-brain (OL-B) circadian GSH system and its ability to deal with reactive oxygen species (ROS) produced as a consequence of metabolic rhythms and light variations. We characterized daily and antioxidant circadian variations of the different parameters of the glutathione system, including GSH, oxidized glutathione (GSSG), glutathione reductase (GR) and glutathione peroxidase (GPx), as well as metabolic and lipoperoxidative circadian oscillations in retina and OL-B, determining internal and external GSH-system synchrony. The results demonstrate statistically significant bi- and unimodal daily and circadian rhythms in all GSH-cycle parameters, substrates and enzymes in OL-B and retina, as well as an apparent direct effect of light on these rhythms, especially in the retina. The luminous condition appears to stimulate the GSH system to antagonize ROS and lipid peroxidation (LPO) daily and circadian rhythms occurring in both structures, oscillating with higher LPO under dark conditions. We suggest that the difference in the effect of light on GSH rhythmic mechanisms of both structures for antagonizing ROS could be due to differences in glutathione-system coupling strength with the circadian clock.     

The circadian control of skin and cutaneous photodamage(†)

Biologically, light including ultraviolet (UV) radiation is vital for life. However, UV exposure does not come without risk, as it is a major factor in the development of skin cancer. Natural protections against UV damage may have been affected by lifestyle changes over the past century, including changes in our sun exposure due to working environments, and the use of sunscreens. In addition, extended "day time" through the use of artificial light may contribute to the disruption of our circadian rhythms; the daily cycles of changes in critical bio-factors including gene expression. Circadian disruption has been implicated in many health conditions, including cardiovascular, metabolic and psychiatric diseases, as well as many cancers. Interestingly, the pineal hormone melatonin plays a role in both circadian regulation as well as protection from UV skin damage, and is therefore an important factor to consider when studying the impact of UV light. This review discusses the beneficial and deleterious effects of solar exposure, including UV skin damage, Vitamin D production, circadian rhythm disruption and the impact of melatonin. Understanding these benefits and risks is critical for the development of protective strategies against solar radiation.     

Real-time cell electrophysiology using a multi-channel dielectrophoretic-dot microelectrode array

Dielectrophoresis (DEP) has been used for many years for the analysis of the electrophysiological properties of cells. However, such analyses have in the past been time-consuming, such that it can take 30 min or more to collect sufficient data to make valid interpretations from a single DEP spectrum. This has limited the application of the technology to a rapid tool for non-invasive, label-free research in areas from drug discovery to diagnostics. In this paper we present the development of a programmable, multi-channel DEP system for rapid biophysical assessment of populations of biological cells. A new assay format has been developed for continuous near-real-time monitoring, using simultaneous application of up to eight alternating current electrical signals to independently addressable dot microelectrodes in an array format, allowing a DEP spectrum to be measured in 20?s, with a total cycle time between measurements of 90?s. To demonstrate the system, human leukaemic K562 cells were monitored after exposure to staurosporine and valinomycin. The DEP response curves showed the timing and manner in which the membrane properties changed for the actions of these two drugs at the early phase of induction. This technology shows the great potential for increasing our understanding of the role of electrophysiology in drug action, by observing the changes in electrical characteristics as they occur.     

EXTRARETINAL PHOTORECEFTION IN INSECTS

Abstract— Extraretinal photoreceptors are widespread among insects and function in the photoperiodic control of development and in the entrainment of circadian rhythms. The effects of light on the daily and seasonal regulation of brain neuroendocrine activity are mediated solely through extraretinal photoreceptors. In primitive insects, the eyes participate in the entrainment of nonendocrine circadian rhythms such as the locomotor rhythm. In more advanced forms, however, extraretinal pathways appear to be the only pathway for the entrainment of all rhythms thus far examined. But even in this latter case, the eyes sometimes effect a masking of the expression of the overt rhythm. An exact localization of the extraretinal receptors has not been accomplished, but in all studies to date they appear to be associated with the cerebral lobe region of the brain. Action spectra for photoperiodic responses have been determined for a number of insects. In general the responses are maximally sensitive in the blue with a marked decline in the red although exceptions do exist. Complete action spectra for circadian responses have been determined only for two insects. In both cases a plateau of sensitivity extends through the blue with a steep drop at longer wavelengths. From the action spectra data, the extraretinal receptors appear to have a threshold sensitivity less than 3 times 10^-2 J/m². The pigment nature of the receptor is unknown although it appears not to be a carotenoid derivative.     

The surface conductance of red blood cells and platelets is modulated by the cell membrane potential

Dielectrophoretic analysis of cell electrical properties via the Clausius–Mossotti model has been widely used to estimate values of the membrane conductance, membrane capacitance and cytoplasm conductivity of cells. However, although the latter two values produced by this method compare well to those acquired by other electrophysiological methods, the membrane conductance is often substantially larger than that acquired by methods such as patch clamp. In this paper, the electrical properties of red blood cells (RBC) are analysed at two conductivities and following membrane-altering treatments, to develop a mathematical model of membrane conductance. Results suggest that the RBC “membrane conductance” term is primarily dominated by surface conduction, comprising an element related to medium conductivity augmented by conduction in the electrical double layer, which is in turn altered by the cell membrane potential. Validation of the relationship between membrane potential and membrane conductance was performed using platelets, where a similar relationship was observed. This sheds new light on the origin and significance of the membrane conductance term and explains for the first time phenomena of alterations in the parameter counter to changes in membrane potential or cytoplasm conductivity.     

Common features of photoperiodism in plants and animals

Abstract— Light break experiments show the role of the circadian clock in photoperiodic timemeasurement. Additional evidence comes from experiments which show the close relation between temperature- or light-induced phase shifts in cycles of photoperiodic responsiveness and simultaneous phase shifts of other processes which are under control of the circadian clock. Using the circadian clock is a common feature of photoperiodism in plants and animals. This clock controls quantitative and qualitative changes in the responsiveness to light. However, quite different pigment systems may be involved, resulting in different action spectra for light break effects. In many cases, these action spectra differ also from the action spectra for phase shifts in the circadian clock.     

Regulation of the Cyanobacterial Circadian Clock by Electrochemically Controlled Extracellular Electron Transfer

There is growing awareness that circadian clocks are closely related to the intracellular redox state across a range of species. As the redox state is determined by the exchange of the redox species, electrochemically controlled extracellular electron transfer (EC‐EET), a process in which intracellular electrons are exchanged with extracellular electrodes, is a promising approach for the external regulation of circadian clocks. Herein, we discuss whether the circadian clock can be regulated by EC‐EET using the cyanobacterium Synechococcus elongatus PCC7942 as a model system. In vivo monitoring of chlorophyll fluorescence revealed that the redox state of the plastoquionone pool could be controlled with EC‐EET by simply changing the electrode potential. As a result, the endogenous circadian clock of S. elongatus cells was successfully entrained through periodically modulated EC‐EET by emulating the natural light/dark cycle, even under constant illumination conditions. This is the first example of regulating the biological clock by electrochemistry.     

ENTRAINMENT OF HUMAN ORCADIAN RHYTHMS BY LIGHT-DARK CYCLES: A REASSESSMENT

Abstract— Man is the only eukaryotic organism in which it has been reported that the circadian system cannot be entrained to a 24-h period by a simple light-dark (LD) cycle. In this paper, we reexamine the evidence for that claim and demonstrate that there were some fundamental flaws in the experimental design of the previous studies on which this conclusion was based. We report new studies in which we tested the efficacy of LD cycles in entraining the circadian rhythms of human subjects living in isolation from environmental time cues. We found that the cyclic alternation of light and dark, when applied to human subjects in a comparable way to experiments in other species, was an effective entraining agent. Our results and a critical review of the literature indicate that a LD cycle alone can be an effective environmental synchronizer of the human circadian timing system. Other factors, such as the knowledge of time of day, social contacts, the feeding schedule, and the imposed rest-activity schedule may contribute to stable entrainment, although their relative strengths as synchronizers have yet to be determined.     

Incorporation of alpha-hemolysin in different tethered bilayer lipid membrane architectures

Tethered bilayer lipid membranes are stable solid supported model membrane systems. They can be used to investigate the incorporation and function of membrane proteins. In order to study ion translocation mediated via incorporated proteins, insulating membranes are necessary. The architecture of the membrane can have an important effect on both the electrical properties of the lipid bilayer as well as on the possibility to functionally host proteins. Alpha-hemolysin pores have been functionally incorporated into a tethered bilayer lipid membrane coupled to a gold electrode. The protein incorporation has been monitored optically and electrically and the influence of the molecular structure of the anchor lipids on the insertion properties has been investigated.     

EXTRARETINAL PHOTORECEPTION IN ENTRAINMENT OF CRUSTACEAN ORCADIAN RHYTHMS*

Abstract— An attempt was made to determine whether entrainment of the circadian rhythms of locomotor activity and ERG amplitude of the crayfish involved extraretinal photoreception. The results of a variety of experiments involving surgical lesions and localized illumination provided evidence that both rhythms can be entrained via an extraretinal pathway. The data also demonstrate that the caudal photoreceptor is unnecessary for entrainment. Our evidence to date suggests that the extraretinal photoreceptor is located in the supraesophageal ganglion; however, the possibility of photoreceptive input from other regions of the CNS, particularly the optic lobe, has not been eliminated. It is also tentatively concluded that the circadian oscillators for both the locomotor and the ERG amplitude rhythms are located within the supraesophageal ganglion, but more data are needed to confirm this conclusion.     

Improvement of the proton exchange membrane fuel cell performances by optimization of the hot pressing process for membrane electrode assembly

The present study deals with PEM fuel cells, namely with the optimization of the hot pressing process for membrane electrode assembly (MEA) fabrication. Designs of experiments (DoE) have been used for evaluating the effect of hot pressing parameters (pressure, temperature, and time) on the MEA electrical performances. Full factorial 2³ DoE showed that the most important parameter is the pressing temperature. Surface response methodology indicated a non-monotonous behavior of the MEA electrical performances with respect to the pressing temperature. The MEA electrical performances increased with the pressing temperature in the temperature range from 100 to 115 °C, and decreased significantly in the temperature range from 115 to 130 °C. This behavior was attributed to drastic changes of the Nafion® 112 membrane properties and membrane/electrode interface over this temperature range. Observations of the MEA cross-section structure by scanning electron microscopy confirmed such hypotheses. Thermo-mechanical properties of Nafion® as determined by dynamic scanning calorimetry allowed estimating the glass transition temperature at ca. T _g?≈?117 °C in the conditions of the present study. The higher H₂/air fuel cell performance of ca. 0.8 W cm^?2 was obtained with the optimized pressing temperature for MEA fabrication of ca. 115 °C close to the T _g temperature of Nafion® 112, whereas for higher temperature the structure of the Nafion® membrane and of the membrane–electrode interface is damaged.