141 research outputs found

    Efficacy of cisplatin and fluorouracil chemotherapy plus Jianpi Yiqi formula in the treatment of advanced gastric cancer

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    Purpose: To investigate the efficacy of cisplatin and fluorouracil chemotherapy in combination with the Jianpi Yiqi formula in the treatment of advanced gastric cancer.Methods: A total of 64 patients with advanced gastric cancer admitted and treated at Xianyang Central Hospital from April 2019 to October 2021 were recruited and assigned equally to chemotherapy group and combination group according to the time of admission. Chemotherapy group received cisplatin and fluorouracil, while the combination group received the Jianpi Yiqi formula based on the treatment given to the chemotherapy group. Some clinical indices were evaluated in the patients.Results: Intervention in the combination group was associated with a higher total effectiveness when compared with chemotherapy group (p < 0.05). Cisplatin and fluorouracil plus Jianpi Yiqi formula resulted in significantly higher European Organization for Research and Treatment of Cancer Quality of Life Questionnaire Core 30-item (EORTC QLQ-C30) score than cisplatin with fluorouracil (p < 0.05). Furthermore, cisplatin and fluorouracil plus Jianpi Yiqi formula led to considerably higher Karnofsky Performance Scale (KPS) scores versus cisplatin with fluorouracil (p < 0.05).Conclusion: In the treatment of advanced gastric cancer, cisplatin-fluorouracil chemotherapy in conjunction with the Jianpi Yiqi formula produces remarkable efficacy. This strategy increases lesion dissolution rates, improves the quality of life and behavioral status of patients, and reduces adverse reactions, resulting in prolonged patients' progression survival (PFS) and overall survival (OS) levels

    The development of a glossary of contemporary Chinese values and its initial application

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    A value is an outward or inward view of what is β€œworthwhile” and is a belief system that people uses to distinguish between good and bad and to guide their behavior. Values vary from culture to culture and from time to time. In order to develop a vocabulary for measuring the values of contemporary Chinese, an open-ended survey was conducted in Study 1 to collect the value vocabulary of the Chinese public, and a text analysis was conducted in Study 2 to acquire the value vocabulary of the Chinese society. In Study 3, a word list of contemporary Chinese values was developed by integrating the words obtained from the above two studies and combining words from previous studies, and a preliminary application of the word list was conducted. The results revealed that Chinese values include four dimensions: self-fulfillment, self-cultivation, social development, and interpersonal ethics. Chinese values are characterized by diversity, and some of the socially advocated values have been internalized into the value system of individuals

    Inferring activity changes of transcription factors by binding association with sorted expression profiles

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    <p>Abstract</p> <p>Background</p> <p>The identification of transcription factors (TFs) associated with a biological process is fundamental to understanding its regulatory mechanisms. From microarray data, however, the activity changes of TFs often cannot be directly observed due to their relatively low expression levels, post-transcriptional modifications, and other complications. Several approaches have been proposed to infer TF activity changes from microarray data. In some models, a linear relationship between gene expression and TF-gene binding strength is assumed. In some other models, the target genes of a TF are first determined by a significance cutoff to binding affinity scores, and then expression differentiation is checked between the target and other genes.</p> <p>Results</p> <p>We propose a novel method, referred to as BASE (binding association with sorted expression), to infer TF activity changes from microarray expression profiles with the help of binding affinity data. It searches the maximum association between bind affinity profile of a TF and expression change profile along the direction of sorted differentiation. The method does not make hard target gene selection, rather, the significances of TF activity changes are evaluated by permutation tests of binding association at the end. To show the effectiveness of this method, we apply it to three typical examples using different kinds of binding affinity data, namely, ChIP-chip data, motif discovery data, and positional weighted matrix scanning data, respectively. The implications obtained from all three examples are consistent with established biological results. Moreover, the inferences suggest new and biological meaningful hypotheses for further investigation.</p> <p>Conclusion</p> <p>The proposed method makes transcription inference from profiles of expression and binding affinity. The same machinery can be used to deal with various kinds of binding affinity data. The method does not require a linear assumption, and has the desirable property of scale-invariance with respect to TF-specific binding affinity. This method is easy to implement and can be routinely applied for transcriptional inferences in microarray studies.</p

    Neural activity dissociation between thought-based and perception-based response conflict

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    Based on the idea that intentions have different penetrability to perception and thought (Fodor, 1983), four Stroop-like tasks, AA, AW, WA, and WW are used, where the A represents an arrow and the CPPR (closest processing prior to response) is perception, and the W represents a word and the CPPR is thought. Event-related brain potentials were recorded as participants completed these tasks, and sLORETA (standardized low resolution brain electromagnetic tomography) was used to localize the sources at specific time points. These results showed that there is an interference effect in the AA and WA tasks, but not in the AW or WW tasks. The activated brain areas related to the interference effect in the AA task were the PFC and ACC, and PFC activation took place prior to ACC activation; but only PFC in WA task. Combined with previous results, a new neural mechanism of cognitive control is proposed

    Visual duration aftereffect is position invariant

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    Adaptation to relatively long or short sensory events leads to a negative aftereffect, such that the durations of the subsequent events within a certain range appear to be contracted or expanded. The distortion in perceived duration is presumed to arise from the adaptation of duration detectors. Here, we focus on the positional sensitivity of those visual duration detectors by exploring whether the duration aftereffect may be constrained by the visual location of stimuli. We adopted two different paradigms, one that tests for transfer across visual hemifields, and the other that tests for simultaneous selectivity between visual hemifields. By employing these experimental designs, we show that the duration aftereffect strongly transfers across visual hemifields and is not contingent on them. The lack of position specificity suggests that duration detectors in the visual system may operate at a relatively later stage of sensory processing

    Correlation of microsynteny conservation and disease gene distribution in mammalian genomes

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    <p>Abstract</p> <p>Background</p> <p>With the completion of the whole genome sequence for many organisms, investigations into genomic structure have revealed that gene distribution is variable, and that genes with similar function or expression are located within clusters. This clustering suggests that there are evolutionary constraints that determine genome architecture. However, as most of the evidence for constraints on genome evolution comes from studies on yeast, it is unclear how much of this prior work can be extrapolated to mammalian genomes. Therefore, in this work we wished to examine the constraints on regions of the mammalian genome containing conserved gene clusters.</p> <p>Results</p> <p>We first identified regions of the mouse genome with microsynteny conservation by comparing gene arrangement in the mouse genome to the human, rat, and dog genomes. We then asked if any particular gene types were found preferentially in conserved regions. We found a significant correlation between conserved microsynteny and the density of mouse orthologs of human disease genes, suggesting that disease genes are clustered in genomic regions of increased microsynteny conservation.</p> <p>Conclusion</p> <p>The correlation between microsynteny conservation and disease gene locations indicates that regions of the mouse genome with microsynteny conservation may contain undiscovered human disease genes. This study not only demonstrates that gene function constrains mammalian genome organization, but also identifies regions of the mouse genome that can be experimentally examined to produce mouse models of human disease.</p

    PERK Activation Promotes Medulloblastoma Tumorigenesis by Attenuating Premalignant Granule Cell Precursor Apoptosis.

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    Evidence suggests that activation of pancreatic endoplasmic reticulum kinase (PERK) signaling in response to endoplasmic reticulum stress negatively or positively influences cell transformation by regulating apoptosis. Patched1 heterozygous deficient (Ptch1(+/-)) mice reproduce human Gorlin's syndrome and are regarded as the best animal model to study tumorigenesis of the sonic hedgehog subgroup of medulloblastomas. It is believed that medulloblastomas in Ptch1(+/-) mice results from the transformation of granule cell precursors (GCPs) in the developing cerebellum. Here, we determined the role of PERK signaling on medulloblastoma tumorigenesis by assessing its effects on premalignant GCPs and tumor cells. We found that PERK signaling was activated in both premalignant GCPs in young Ptch1(+/-) mice and medulloblastoma cells in adult mice. We demonstrated that PERK haploinsufficiency reduced the incidence of medulloblastomas in Ptch1(+/-) mice. Interestingly, PERK haploinsufficiency enhanced apoptosis of premalignant GCPs in young Ptch1(+/-) mice but had no significant effect on medulloblastoma cells in adult mice. Moreover, we showed that the PERK pathway was activated in medulloblastomas in humans. These results suggest that PERK signaling promotes medulloblastoma tumorigenesis by attenuating apoptosis of premalignant GCPs during the course of malignant transformation.Grant numbers and sources of support: National Institutes of Health (NS73132, NS37956, and CA21765), National Multiple Sclerosis Society (RG4813-A-2 and RG5239-A-3), and Wellcome Trust.This is the final version of the article. It first appeared from Elsevier via https://doi.org/10.1016/j.ajpath.2016.03.00

    The Effects of Same- and Other-Race Facial Expressions of Pain on Temporal Perception

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    Previous studies suggested that threatening stimuli lengthen subjective duration, while facial expressions of pain were found to produce a shortening effect on temporal perception in a recent study. Moreover, individuals’ responses to others’ pain were influenced by the individuals’ relationship to a racial group. However, the effects of same- and other-race pained facial expressions on temporal perception, remain unknown. The aim of this present study was to identify the effect expressions of pain have on temporal perception and to explore whether this effect was modulated by the relationship to a racial group. In a temporal bisection task, Chinese participants were presented with pain or neutral facial expressions displayed by Caucasian (other-race) or Chinese (same-race) models in a 400–1600 ms or 200–800 ms condition. Expressions of pain were rated as more arousing, negative and disagreeable, than neutral facial expressions. These scores were not significantly different between same- and other-race facial expressions. Based on the results of the temporal bisection task, both same- and other-race pained facial expressions lengthened the perceived duration in the 400–1600 ms condition, but only same-race pained facial expressions produced this effect in the 200–800 ms condition. We postulate that the existence of a short-lived effect of pained facial expressions on lengthening temporal perception caused by arousal and attention, occurs at an earlier time point for same-race pained facial expressions than for other-race pained facial expressions

    Genomic Androgen Receptor-Occupied Regions with Different Functions, Defined by Histone Acetylation, Coregulators and Transcriptional Capacity

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    Background: The androgen receptor (AR) is a steroid-activated transcription factor that binds at specific DNA locations and plays a key role in the etiology of prostate cancer. While numerous studies have identified a clear connection between AR binding and expression of target genes for a limited number of loci, high-throughput elucidation of these sites allows for a deeper understanding of the complexities of this process. Methodology/Principal Findings: We have mapped 189 AR occupied regions (ARORs) and 1,388 histone H3 acetylation (AcH3) loci to a 3 % continuous stretch of human genomic DNA using chromatin immunoprecipitation (ChIP) microarray analysis. Of 62 highly reproducible ARORs, 32 (52%) were also marked by AcH3. While the number of ARORs detected in prostate cancer cells exceeded the number of nearby DHT-responsive genes, the AcH3 mark defined a subclass of ARORs much more highly associated with such genes – 12 % of the genes flanking AcH3+ARORs were DHT-responsive, compared to only 1 % of genes flanking AcH32ARORs. Most ARORs contained enhancer activities as detected in luciferase reporte
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