Effect of temozolomide combined with radiotherapy on survival and MGMT protein expression in recurrent malignant glioma patients

Purpose: To investigate the effect of temozolomide (TMZ) combined with radiotherapy (RT) on O-6- methylguanine-DNA methyltransferase (MGMT) protein and survival of recurrent malignant glioma patients. Methods: Ninety-two patients with malignant glioma in our hospital from January 2014 to January 2015 were assigned to study and control groups using the random table method. Subjects in the control group received radiotherapy (total dose in the range of 60 – 75 Gy), while those in the study group were given TMZ orally (75 mg/m2) daily in addition to radiotherapy, as well as TMZ at 150 – 200 mg/m2. After treatment, clinical effectiveness was compared for the two groups. Changes in methylation of MGMT gene were determined in the two groups. The patients were followed up for 3 years, and the degrees of survival and recurrence were recorded. Results: Total effectiveness of clinical treatment was markedly higher in the study group (76.09 %) than in the control group (45.65 %; p < 0.05). One month after radiotherapy, significant decrease in MGMT gene methylation was seen in patients in the study group, relative to control patients (p < 0.05). Patients in the study group had lower median recurrence but higher degree of survival in the 2nd and 3rd years, relative to control patients (p < 0.05). Conclusion: The combination of temozolomide and radiotherapy is more effective than radiotherapy in the treatment of recurrent malignant glioma. The combined treatment significantly inhibits tumor recurrence in patients, and improves their prognosis and standard of life

Mitochondrial Genome of an 8,400-Year-Old Individual from Northern China Reveals a Novel Sub-Clade under C5d

Ancient DNA studies have always refreshed our understanding of the human past that can’t be tracked by modern DNA alone. Until recently, ancient mitochondrial genomic studies in East Asia are still very limited. Here, we retrieved the whole mitochondrial genome of an 8,400-year- old individual from Inner Mongolia, China. Phylogenetic analyses show that the individual belongs to a previously undescribed clade under haplogroup C5d that was most probably originated in northern Asia and may have a very low frequency in extant populations that is not yet sampled. We further characterized the demographic history of mitochondrial haplogroups C5 and C5d, and found that C5 experienced a sharp increase in population size starting from around 4,000 years before present (BP). The time when intensive millet farming was built by populations who are associated with the lower Xiajiadian culture and was widely adopted in northern China. We caution that people related to haplogroup C5 may added this farming technology to their original way of life and that the various subsistence may provide abundant food sources and may further contribute to the increase of the population size

Ancient mitochondrial genomes reveal extensive genetic influence of the steppe pastoralists in Western Xinjiang

The population prehistory of Xinjiang has been a hot topic among geneticists, linguists, and archaeologists. Current ancient DNA studies in Xinjiang exclusively suggest an admixture model for the populations in Xinjiang since the early Bronze Age. However, almost all of these studies focused on the northern and eastern parts of Xinjiang; the prehistoric demographic processes that occurred in western Xinjiang have been seldomly reported. By analyzing complete mitochondrial sequences from the Xiabandi (XBD) cemetery (3,500–3,300 BP), the up-to-date earliest cemetery excavated in western Xinjiang, we show that all the XBD mitochondrial sequences fall within two different West Eurasian mitochondrial DNA (mtDNA) pools, indicating that the migrants into western Xinjiang from west Eurasians were a consequence of the early expansion of the middle and late Bronze Age steppe pastoralists (Steppe_MLBA), admixed with the indigenous populations from Central Asia. Our study provides genetic links for an early existence of the Indo-Iranian language in southwestern Xinjiang and suggests that the existence of Andronovo culture in western Xinjiang involved not only the dispersal of ideas but also population movement.Introduction Materials and methods - Archaeological Background, Sampling, and Sequencing - Sequence Mapping and Mitochondrial DNA Haplogroup Determination - Analysis of Xiabandi Mitochondrial DNA Genomes Results - Mitochondrial DNA Authentication and Contamination Assessment - Major Bronze Age Steppe Pastoralist Origin of the Xiabandi Mitochondrial Haplogroups - Expansion of the Bronze Age Steppe Pastoralists as a Dynamic Process to Form the Genetic Landscape of Xiabandi Individuals Discussion Conclusion

Exploring the Potential Transmission Risk of Schistosomiasis Japonica in the Lower Reaches of the Yangtze River, China

Vector snails are important in the life cycle of schisosomiasis, the need to understand the ecologic factors that could enhance snails’ survival and trigger schistosomiasis transmission necessitated this study. Therefore, the potential risk of schistosomiasis transmission was explored in Zhangjiagang region, a non-endemic area in lower reaches of Yangtze River, eastern of China. The key indictors, including snail survival rate, spawn rate, hatching rate and gland development, were investigated through the designed experiments, routine snail and infectious source surveillance. The results showed that there was no significant difference in surviving rate, spawn rate, hatching rate and gland development between groups of simulated environments in laboratory, similar finding in field experiments, which suggested that snails stand a high possibility to survive in these non-endemic areas once they spread into these areas from other places. And no snails and infectious source were found either in the previous routine monitoring in the past decades and the snail surveillance we conducted from 2007 to 2013. Therefore, there is little risk in the study areas in the lower reaches of the Yangtze River. However, the sporadic and imported cases are still seen in a few areas adjacent to the endemic or transmission interrupted areas as the important infectious source, thus become a risk of schistosomisis transmission or re-emergence in these areas where the snail exists. Hence, maintaining routine monitoring and surveillance can be one of the effective and efficient ways to prevent the re-emergence of Schistosomiasis

Association Between Single Nucleotide Polymorphisms in PPARA and EPAS1 Genes and High-Altitude Appetite Loss in Chinese Young Men

Appetite loss is a common symptom that occurs in high altitude (HA) for lowlanders. Previous studies indicated that hypoxia is the initiating vital factor of HA appetite loss. PPARA, EPAS1, EGLN1, HIF1A, HIF1AN, and NFE2L2 play important roles in hypoxic responses. We aimed to explore the association of these hypoxia-related gene polymorphisms with HA appetite loss. In this study, we enrolled 416 young men who rapidly ascended to Lhasa (3700 m) from Chengdu (<500m) by plane. PPARA, EPAS1, EGLN1, HIF1A, HIF1AN, and NFE2L2 were genotyped by MassARRAY. Appetite scores were measured to identify HA appetite loss. Logistic regression and multiple genetic models were tested to evaluate the association between the single nucleotide polymorphisms (SNPs) and risk of HA appetite loss in crude and adjusted (age and SaO2) analysis. Subsequently, Haploview software was used to analyze the linkage disequilibrium (LD), haplotype construction and the association of diverse haplotypes with the risk of HA appetite loss. Our results revealed that allele “A” in PPARA rs4253747 was significantly associated with the increased risk of HA appetite loss. Codominant, dominant, recessive, and log-additive models of PPARA rs4253747 showed the increased risk of HA appetite loss in the crude and adjusted analysis. However, only dominant, overdominant, and log-additive models of EPAS1 rs6756667 showed decreased risk of HA appetite loss in the crude and adjusted analysis. Moreover, the results from haplotype-based test showed that the rs7292407-rs6520015 haplotype “AC” was associated with HA appetite loss in the crude analysis rather than the adjusted analysis. In this study, we first established the association of SNPs in PPARA (rs4253747) and EPAS1 (rs6756667) genes with susceptibility to HA appetite loss in Han Chinese young men. These findings provide novel insights into understanding the mechanisms involved in HA appetite loss

Identification and Comparison of microRNAs in the Gonad of the Yellowfin Seabream (Acanthopagrus Latus)

Yellowfin seabream (Acanthopagrus latus) is a commercially important fish in Asian coastal waters. Although natural sex reversal has been described in yellowfin seabream, the mechanisms underlying sexual differentiation and gonadal development in this species remain unclear. MicroRNAs (miRNAs) have been shown to play crucial roles in gametogenesis and gonadal development. Here, two libraries of small RNAs, constructed from the testes and ovaries of yellowfin seabream, were sequenced. Across both gonads, we identified 324 conserved miRNAs and 92 novel miRNAs: 67 ovary-biased miRNAs, including the miR-200 families, the miR-29 families, miR-21, and miR-725; and 88 testis-biased miRNAs, including the let-7 families, the miR-10 families, miR-7, miR-9, and miR-202-3p. GO (Gene Ontology) annotations and KEGG (Kyoto Encyclopedia of Genes and Genomes) enrichment analyses of putative target genes indicated that many target genes were significantly enriched in the steroid biosynthesis pathway and in the reproductive process. Our integrated miRNA-mRNA analysis demonstrated a putative negatively correlated expression pattern in yellowfin seabream gonads. This study profiled the expression patterns of sex-biased miRNAs in yellowfin seabream gonads, and provided important molecular resources that will help to clarify the miRNA-mediated post-transcriptional regulation of sexual differentiation and gonadal development in this species

Development and application of a rapid rehabilitation system for reconstruction of maxillofacial soft-tissue defects related to war and traumatic injuries

Background: The application of a maxillofacial prosthesis is an alternative to surgery in functional-aesthetic facial reconstruction. Computer aided design/computer aided manufacturing has opened up a new approach to the fabrication of maxillofacial prostheses. An intelligentized rapid simulative design and manufacturing system for prostheses was developed to facilitate the prosthesis fabrication procedure

Association of EPAS1 and PPARA Gene Polymorphisms with High-Altitude Headache in Chinese Han Population

Background. High-altitude headache (HAH) is the most common complication after high-altitude exposure. Hypoxia-inducible factor- (HIF-) related genes have been confirmed to contribute to high-altitude acclimatization. We aim to investigate a possible association between HIF-related genes and HAH in the Chinese Han population. Methods. In total, 580 healthy Chinese Han volunteers were recruited in Chengdu (500 m) and carried to Lhasa (3700 m) by plane in 2 hours. HAH scores and basic physiological parameters were collected within 18–24 hours after the arrival. Thirty-five single nucleotide polymorphisms (SNPs) in HIF-related genes were genotyped, and linkage disequilibrium (LD) was evaluated by Haploview software. The functions of SNPs/haplotypes for HAH were developed by using logistic regression analysis. Results. In comparison with wild types, the rs4953354 “G” allele (P=0.013), rs6756667 “A” allele (P=0.036) in EPAS1, and rs6520015 “C” allele in PPARA (P=0.009) were significantly associated with decreased risk of HAH. The rs7292407-rs6520015 haplotype “C-C” in PPARA was identified as a protective factor (P=0.030). Importantly, EPAS1 and PPARA genes have synergistic effects in decreasing HAH risk (P=0.003). Conclusions. EPAS1 and PPARA polymorphisms were associated with HAH in the Chinese Han population. Our findings pointed out potentially predictive gene markers, provided new insights into understanding pathogenesis, and may further provide prophylaxis and treatment strategies for HAH