Obstructive sleep apnea syndrome (OSAS) is a common breathing disorder in sleep in which the airways narrow or collapse during sleep, causing obstructive sleep apnea. The prevalence of OSAS continues to rise worldwide, particularly in middle-aged and elderly individuals. The mechanism of upper airway collapse is incompletely understood but is associated with several factors, including obesity, craniofacial changes, altered muscle function in the upper airway, pharyngeal neuropathy, and fluid shifts to the neck. The main characteristics of OSAS are recurrent pauses in respiration, which lead to intermittent hypoxia (IH) and hypercapnia, accompanied by blood oxygen desaturation and arousal during sleep, which sharply increases the risk of several diseases. This paper first briefly describes the epidemiology, incidence, and pathophysiological mechanisms of OSAS. Next, the alterations in relevant signaling pathways induced by IH are systematically reviewed and discussed. For example, IH can induce gut microbiota (GM) dysbiosis, impair the intestinal barrier, and alter intestinal metabolites. These mechanisms ultimately lead to secondary oxidative stress, systemic inflammation, and sympathetic activation. We then summarize the effects of IH on disease pathogenesis, including cardiocerebrovascular disorders, neurological disorders, metabolic diseases, cancer, reproductive disorders, and COVID-19. Finally, different therapeutic strategies for OSAS caused by different causes are proposed. Multidisciplinary approaches and shared decision-making are necessary for the successful treatment of OSAS in the future, but more randomized controlled trials are needed for further evaluation to define what treatments are best for specific OSAS patients. 

/pdf/pathophysiological-mechanisms-and-therapeutic-approaches-in-m13znu94.pdf

Pathophysiological mechanisms and therapeutic approaches in obstructive sleep apnea syndrome

Intervertebral disc degeneration (IDD) is the major cause of low back pain which incurs a significant public-health and economic burden. The aetiology of IDD is complex, with developmental, genetic, biomechanical and biochemical factors contributing to the disease development. Deregulated phenotypes of nucleus pulposus cells, including aberrant differentiation, apoptosis, proliferation and extracellular matrix deposition, are involved in the initiation and progression of IDD. Non-coding RNAs, including long non-coding RNAs (lncRNAs), have recently been identified as important regulators of gene expression. Research into their roles in IDD has been very active over the past 5 years. Our review summarizes current research regarding the roles of deregulated lncRNAs (eg, RP11-296A18.3, TUG1, HCG18) in modulating nucleus pulposus cell functions in IDD. These exciting findings suggest that specific modulation of lncRNAs or their downstream signalling pathways might be an attractive approach for developing novel therapeutics for IDD.

/pdf/long-non-coding-rnas-in-nucleus-pulposus-cell-function-and-16w9fw4i47.pdf

Long non-coding RNAs in nucleus pulposus cell function and intervertebral disc degeneration

BACKGROUND/AIMS Long non-coding RNAs (lncRNAs) acting as competing endogenous RNAs (ceRNAs) play significant roles in the development of tumors, but the functions of specific lncRNAs and lncRNA-related ceRNA networks have not been fully elucidated for colon adenocarcinoma (COAD). In this study, we aimed to clarify the lncRNA-microRNA (miRNA)-mRNA ceRNA network and potential lncRNA biomarkers in COAD. METHODS We extracted data from The Cancer Genome Atlas (TCGA) and identified COAD-specific mRNAs, miRNAs, and lncRNAs. The biological processes in Gene Ontology (GO) and the Kyoto Encyclopedia of Genes and Genomes (KEGG) were analyzed for COAD-specific mRNAs. We then constructed a ceRNA network of COAD-specific mRNAs, miRNAs and lncRNAs and analyzed the correlation between expression patterns and clinical features of the lncRNAs involved. After identifying potential mRNA targets of 4 lncRNAs related to overall survival (OS), we conducted stepwise analysis of these targets through GO and KEGG. Using tissue samples from our own patients, we also verified certain analytical results using quantitative real-time PCR (qRT-PCR). RESULTS Data from 521 samples (480 tumor tissue and 41 adjacent non-tumor tissue samples) were extracted from TCGA. A total of 258 specific lncRNAs, 206 specific miRNAs, and 1467 specific mRNAs were identified (absolute log2 [fold change] > 2, false discovery rate < 0.01). Analysis of KEGG revealed that specific mRNAs were enriched in cancer-related pathways. The ceRNA network was constructed with 64 lncRNAs, 18 miRNAs, and 42 mRNAs. Among these lncRNAs involved in the network, 3 lncRNAs (LINC00355, HULC, and IGF2-AS) were confirmed to be associated with certain clinical features and 4 lncRNAs (HOTAIR, LINC00355, KCNQ1OT1, and TSSC1-IT1) were found to be negatively linked to OS (log-rank p < 0.05). KEGG showed that the potential mRNA targets of these 4 lncRNAs may be concentrated in the MAPK pathway. Certain results were validated by qRT-PCR. CONCLUSION This study providing novel insights into the lncRNA-miRNA-mRNA ceRNA network and reveals potential lncRNA biomarkers in COAD.

/pdf/analysis-of-lncrna-associated-cerna-network-reveals-5kdnqzp6zo.pdf

Analysis of lncRNA-Associated ceRNA Network Reveals Potential lncRNA Biomarkers in Human Colon Adenocarcinoma

SP1-induced ZFAS1 aggravates sepsis-induced cardiac dysfunction via miR-590-3p/NLRP3-mediated autophagy and pyroptosis.

In the past decade, there has been a shift in research, clinical development, and commercial activity to exploit the many physiological roles of RNA for use in medicine. With the rapid success in the development of lipid–RNA nanoparticles for mRNA vaccines against COVID-19 and with several approved RNA-based drugs, RNA has catapulted to the forefront of drug research. With diverse functions beyond the role of mRNA in producing antigens or therapeutic proteins, many classes of RNA serve regulatory roles in cells and tissues. These RNAs have potential as new therapeutics, with RNA itself serving as either a drug or a target. Here, based on the CAS Content Collection, we provide a landscape view of the current state and outline trends in RNA research in medicine across time, geography, therapeutic pipelines, chemical modifications, and delivery mechanisms.

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9115888

The Progress and Promise of RNA Medicine—An Arsenal of Targeted Treatments

It is estimated that more than 90% of the mammalian genome is transcribed as non-coding RNAs. Recent evidences have established that these non-coding transcripts are not junk or just transcriptional noise, but they do serve important biological purpose. One of the rapidly expanding fields of this class of transcripts is the regulatory lncRNAs, which had been a major challenge in terms of their molecular functions and mechanisms of action. The emergence of high-throughput technologies and the development in various conventional approaches have led to the expansion of the lncRNA world. The combination of multidisciplinary approaches has proven to be essential to unravel the complexity of their regulatory networks and helped establish the importance of their existence. Here, we review the current methodologies available for discovering and investigating functions of long non-coding RNAs (lncRNAs) and focus on the powerful technological advancement available to specifically address their functional importance.

Technological Developments in lncRNA Biology.

Biological functions of nanofiber scaffolds can be engineered via the incorporation of plant extracts. In the present study, Emblica officinalis (EO) (Indian Gooseberry known as amla)-loaded poly(e-caprolactone) (PCL) nanofibers were prepared via the electrospinning technique. The aim was to prepare nanofiber scaffolds with antibacterial and anti-cancerous properties. The scaffolds were characterized via SEM, XRD, small-angle X-ray scattering, FTIR spectroscopy, streaming potential, DSC, water contact angle and tensile measurements. Upon the incorporation of EO, the nanofiber surface became rougher and exhibited a ‘braid-like’ morphology. This is in contrast to the pristine PCL nanofibers, which exhibited a smooth fiber surface. The average fiber diameter increased, and the water contact angle of the nanofiber scaffolds decreased with an increase in the EO content in PCL. The crystalline structure of PCL was not affected; however, its crystallization temperature increased significantly and its melting temperature increased marginally with the addition of EO. The PCL scaffold showed a negatively charged surface and its ξ-potential increased with an increase in EO content due to the presence of various functional groups. The antibacterial studies revealed that the PCL–EO nanofiber scaffolds exhibited efficient antibacterial properties against both Gram-positive and Gram-negative bacterial strains and the zone of inhibition increased with EO content. Furthermore, cellular behavior of MCF-7 cells was studied using the MTT assay, fluorescent staining and SEM, which indicated that cell proliferation was significantly inhibited by the incorporation of EO in the scaffolds.

/pdf/emblica-officinalis-loaded-poly-e-caprolactone-electrospun-10ptub7t52.pdf

Emblica officinalis-loaded poly(ε-caprolactone) electrospun nanofiber scaffold as potential antibacterial and anticancer deployable patch

In this paper, we present a novel approach for Human Computer Interaction (HCI) where, we control cursor movement using a real-time camera. Current methods involve changing mouse parts such as adding more buttons or changing the position of the tracking ball. Instead, our method is to use a camera and computer vision technology, such as image segmentation and gesture recognition, to control mouse tasks (left and right clicking, double-clicking, and scrolling) and we show how it can perform everything as current mouse devices can. The software will be developed in JAVA language. Recognition and pose estimation in this system are user independent and robust as we will be using colour tapes on our finger to perform actions. The software can be used as an intuitive input interface to applications that require multi-dimensional control e.g. computer games etc.

Mouse Simulation Using Two Coloured Tapes

One of the most important senses in human life is vision, without it one’s life is totally filled with darkness. According to WHO globally millions of people are visually impaired estimated there are 285 million, of whom some millions are blind. Unfortunately, there are around 2.4 million people are blind in our beloved country Pakistan. Human are a crucial part of society and the blind community is a main part of society. The technologies are grown so far to make the life of humans easier more comfortable and more reliable for. However, this disability of the blind community would reduce their chance of using such innovative products. Therefore, the visually impaired community believe that they are burden to other societies and they do not capture in normal activities separates the blind people from society and because of this believe did not participate in the normally tasks of society. The visual impair people mainly face most of the problems in this real-time The aim of this work is to turn the real time world into an audio world by telling blind person about the objects in their way and can read printed text. This will enable blind persons to identify the things and read the text without any external help just by using the object detection and reading system in real time. Objective of this work: i) Object detection ii) Read printed text, using state-of-the-art (SOTA) technology.

Advanced Audio Aid for Blind People

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Technological Developments in lncRNA Biology.

Emblica officinalis-loaded poly(ε-caprolactone) electrospun nanofiber scaffold as potential antibacterial and anticancer deployable patch

Mouse Simulation Using Two Coloured Tapes

Mouse Simulation Using Two Coloured Tapes

Advanced Audio Aid for Blind People