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Features and Controlling Factors of Epigenic Karstification of the Ordovician Carbonates in Akekule Arch,Tarim Basin 被引量:4
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作者 陈强路 赵永强 +2 位作者 李国蓉 储呈林 王斌 《Journal of Earth Science》 SCIE CAS CSCD 2012年第4期506-515,共10页
ABSTRACT: Tabei (塔北) uplift is an area with the highest hydrocarbon enrichment in Tarim basin, and large oilfields have been found on Akekule (阿克库勒) arch at the middle section of Tabei uplift, with Ordovici... ABSTRACT: Tabei (塔北) uplift is an area with the highest hydrocarbon enrichment in Tarim basin, and large oilfields have been found on Akekule (阿克库勒) arch at the middle section of Tabei uplift, with Ordovician carbonate reservoirs. Storage space of the Ordovician carbonate reservoirs in the Akekule arch are mainly caves, pores and fractures resulted from dissolution and/or karstification. The Ordovician carbonate reservoirs are affected and modified by the diagenetie process in penecontemporaneous, epigenetic and burial periods and the multi-stage karstification related with deep hydrothermal activities, among which the most significant effect is from the meteoric water karstification related to the tectonic uplift from the end of Middle Ordovician to the end of Late Ordovician (end of O2-end of 03) and at the end of Middle Devonian (end of D2). Varied palacogeologic settings and tectonic features at different geologic periods lead to different fluid flowing patterns, karstification mechanisms and transformation features in different regions, which further influence the reservoir distribution. The paleo-uplifts at different periods, such as end of O2-end of 03 and end of D2, control the dominant development zones of karstification; the paleogeomorphology and faults resulted from tectonic uplift control the flowing depth of the karst fluid; and the lithology controls the position and extent of karst development. 展开更多
关键词 epigenic karstification carbonate rock ORDOVICIAN controlling factor Akekule arch Tarim basin.
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牙鲆epigen基因的克隆以及在变态过程中的表达 被引量:6
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作者 谢彩霞 邢巨斌 鲍宝龙 《上海海洋大学学报》 CAS CSCD 北大核心 2010年第5期577-582,共6页
为了调查表皮细胞分裂原epigen基因是否与牙鲆变态发育有关,分析了从变态期牙鲆仔鱼cDNA文库中测序得到的epigen基因。发现epigen基因编码162个氨基酸,具有信号肽序列,一个跨膜结构域和EGF-like结构域。EGF-like结构域包含有可形成3个... 为了调查表皮细胞分裂原epigen基因是否与牙鲆变态发育有关,分析了从变态期牙鲆仔鱼cDNA文库中测序得到的epigen基因。发现epigen基因编码162个氨基酸,具有信号肽序列,一个跨膜结构域和EGF-like结构域。EGF-like结构域包含有可形成3个二硫键的6个半胱氨酸残基,是表皮生长因子家族的结构特征。此外,利用荧光实时定量RT-PCR,调查了epigen基因在牙鲆眼睛移动过程中的变化。相比眼睛移动之前(17DAH,day after hatching),epigen基因在眼睛移动初期(19DAH)表达明显增强,为17DAH时的2.363倍;而在眼睛移动过程的高峰期(23DAH),表达量明显回落,相对19DAH的表达量降低了80%;变态结束后(27DAH)epigen基因的表达没有重新增强或进一步的回落,提示epigen基因可能与眼睛移动初期的变态发育事件有关,而与变态高峰期和变态后期的发育事件关系不明显。 展开更多
关键词 牙鲆 epigen基因 实时定量PCR 表皮生长因子
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表皮调节素、上皮有丝分裂原和干细胞因子对山羊精原干细胞增殖的影响
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作者 李浩 方乾 +3 位作者 任发 代贵超 王立强 胡建宏 《家畜生态学报》 北大核心 2020年第3期47-51,共5页
为了揭示表皮调节素(Epiregulin/EREG)、上皮有丝分裂原(Epigen/EPG)和干细胞因子(SCF)对山羊精原干细胞(SSCs)增殖的影响,改进SSCs体外培养体系。在含有胶质细胞源性神经营养因子(GDNF)、碱性成纤维细胞生长因子(bFGF)和白细胞抑制因子... 为了揭示表皮调节素(Epiregulin/EREG)、上皮有丝分裂原(Epigen/EPG)和干细胞因子(SCF)对山羊精原干细胞(SSCs)增殖的影响,改进SSCs体外培养体系。在含有胶质细胞源性神经营养因子(GDNF)、碱性成纤维细胞生长因子(bFGF)和白细胞抑制因子(LIF)的SSCs培养基基础上,分别添加20 ng/mL干细胞因子、20 ng/mL表皮调节素、20 ng/mL和100 ng/mL上皮有丝分裂原。对富集后山羊SSCs进行12 d的培养,测定培养过程中山羊SSCs生长曲线和细胞活性。结果表明:添加100 ng/mL上皮有丝分裂原和20 ng/mL的表皮调节素相比其他组能够显著促进山羊SSCs的体外增殖和细胞活力(P<0.05);其中培养12 d后添加20 ng/mL表皮调节素的细胞活力显著高于其他组,但细胞数量与100 ng/mL上皮有丝分裂原组无显著差异。20 ng/mL SCF相比对照组能够显著提高体外增殖和细胞活力(P<0.05),但低于100 ng/mL上皮有丝分裂原和20 ng/mL表皮调节素组(P>0.05)。因此,添加100 ng/mL上皮有丝分裂原、20 ng/mL干细胞因子和20 ng/mL表皮调节素能够提高山羊SSCs的增殖,其中添加20 ng/mL表皮调节素效果最佳。 展开更多
关键词 山羊精原干细胞 EPIREGULIN EPIGEN SCF 干细胞增殖
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牙鲆变态发育过程中epigen基因的空间表达分布 被引量:4
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作者 李乐康 鲍宝龙 《上海海洋大学学报》 CAS CSCD 北大核心 2012年第6期929-934,共6页
细胞分裂在鲽形目鱼类变态过程中发挥了重要作用。Epigen作为表皮分裂原,通过激活MAPK通道来调控有丝分裂。以前的研究利用定量PCR表明,epigen在变态前期表达量升高,而变态后期表达量下降,表明其与变态发育相关。为了进一步调查epigen... 细胞分裂在鲽形目鱼类变态过程中发挥了重要作用。Epigen作为表皮分裂原,通过激活MAPK通道来调控有丝分裂。以前的研究利用定量PCR表明,epigen在变态前期表达量升高,而变态后期表达量下降,表明其与变态发育相关。为了进一步调查epigen与牙鲆变态发育的关系,利用RNA整体原位杂交技术检测了epigen在变态期牙鲆体内的空间表达分布,发现在变态期的各个阶段,epigen基因表达分布均比较广泛,表皮、鳃、肝脏、肠道、鳍条、支鳍骨、肌节等组织都有表达,在牙鲆变态前和变态早期(E期)信号较强,而在变态高峰期(F期和G期)和变态后期(H期)信号逐渐变弱。Epigen空间表达分布模式提示,其作为表皮分裂原,可能广泛参与牙鲆变态发育早期事件,尤其可能与肝脏、肠道、支鳍骨和鳍条的发育有关。 展开更多
关键词 牙鲆 变态 EPIGEN 整体原位杂交
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Field cancerisation in colorectal cancer:A new frontier or pastures past?
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作者 Abhilasha Patel Gyanendra Tripathi +2 位作者 Kishore Gopalakrishnan Nigel Williams Ramesh P Arasaradnam 《World Journal of Gastroenterology》 SCIE CAS 2015年第13期3763-3772,共10页
Despite considerable advances in our understanding of cancer biology, early diagnosis of colorectal cancer remains elusive. Based on the adenoma-carcinoma sequence, cancer develops through the progressive accumulation... Despite considerable advances in our understanding of cancer biology, early diagnosis of colorectal cancer remains elusive. Based on the adenoma-carcinoma sequence, cancer develops through the progressive accumulation of mutations in key genes that regulate cell growth. However, recent mathematical modelling suggests that some of these genetic events occur prior to the development of any discernible histological abnormality. Cells acquire pro-tumourigenic mutations that are not able to produce morphological change but predispose to cancer formation. These cells can grow to form large patches of mucosa from which a cancer arises. This process has been termed "field cancerisation". It has received little attention in the scientific literature until recently. Several studies have now demonstrated cellular, genetic and epigenetic alterations in the macroscopically normal mucosa of colorectal cancer patients. In some reports, these changes were effectively utilised to identify patients with a neoplastic lesion suggesting potential application in the clinical setting. In this article, we present the scientific evidence to support field cancerisation in colorectal cancer and discuss important limitations that require further investigation. Characterisation of the field defect is necessary to enable early diagnosis of colorectal cancer and identify molecular targets for chemoprevention. Field cancerisation offers a promising prospect for experimental cancer research and has potential to improve patient outcomes in the clinical setting. 展开更多
关键词 COLORECTAL cancer CARCINOGENESIS Biomarkers EPIGEN
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通过饮食多酚进行表观遗传修饰和肿瘤化学预防(英文)
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作者 AjayGOEL 《中国药理学与毒理学杂志》 CAS CSCD 北大核心 2015年第S1期12-12,共1页
Growing evidence indicates that cancer incidence across the world is not similar,and it is more prevalent in certain populations than others,suggesting the critical role for dietary and lifestyle factors.For instance ... Growing evidence indicates that cancer incidence across the world is not similar,and it is more prevalent in certain populations than others,suggesting the critical role for dietary and lifestyle factors.For instance cancer incidence among people from the Indian subcontinent,where most spices are consumed,is much lower than that in the Western World.Spices have been consumed for centuries for a variety of purposes e.g.as flavoring agents,colorants,and preservatives.However,there is increasing evidence for the importance of plant-based foods in regular diet to lowering the risk of most chronic diseases,so spices are now emerging as more than just flavor aids,but as agents that can not only prevent but may even treat disease.Besides suppressing inflammatory pathways,spice-derived nutraceuticals can suppress survival,proliferation,invasion,and angiogenesis of tumor cells.Increasing evidence indicates that genetic alterations are relatively rare,and epigenetic changes(DNA methylation,histone modifications and expression of noncoding RNAs)plays a bigger role in human cancer,and can be easily influenced by environmental,lifestyle and dietary factors,and some estimates suggest that over two-thirds of the cancer incidence can be accounted for by the environmental and dietary factors alone.Among all these factors,diet is probably the single most important factor which may influence carcinogenesis more comprehensively,because diet is readily modifiable and have the potential to modulate multiple epigenetic processes.Polyphenols in dietary botanicals represent a versatile group of phytochemicals with many potentially beneficial activities in terms of disease prevention.Dietary polyphenols(bioflavanoids)have antioxidant and anti-inflammatory properties that might explain their chemopreventive effects.However,the actual therapeutic potential of these compounds may not have been completely realized due to lack of understanding on the effects of these agents on epigenetic modifications.Recent,but limited evidence indicates that some of the polyphenols,including curcumin(from turmeric),genestein(from soy),EGCG(from green tea),diallyl disulfide(from garlic),sulforaphane(from broccoli)and resveratrol(from grapes)may induce epigenetic changes in various cancer cell lines.This presentation will describe some of the current scientific evidence for the role of epigenetic alterations induced by curcumin and boswellia,in support of their anti-cancer activities,which provides a strong scientific foundation for preclinical and human clinical intervention studies in future. 展开更多
关键词 POLYPHENOLS CANCER CHEMOPREVENTION DIETARY epigene
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Mitochondrial metabolism and cancer therapeutic innovation
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作者 Hongxiang Du Tianhan Xu +2 位作者 Sihui Yu Sufang Wu Jiawen Zhang 《Signal Transduction and Targeted Therapy》 2025年第9期4845-4881,共37页
Mitochondria are dynamic organelles that are essential for cellular energy generation,metabolic regulation,and signal transduction.Their structural complexity enables adaptive responses to diverse physiological demand... Mitochondria are dynamic organelles that are essential for cellular energy generation,metabolic regulation,and signal transduction.Their structural complexity enables adaptive responses to diverse physiological demands.In cancer,mitochondria orchestrate multiple cellular processes critical to tumor development.Metabolic reprogramming enables cancer cells to exploit aerobic glycolysis,glutamine metabolism,and lipid alterations,supporting uncontrolled growth,survival,and treatment resistance.Genetic and epigenetic alterations in mitochondrial and nuclear DNA disrupt oxidative phosphorylation,tricarboxylic acid cycle dynamics,and redox homeostasis,driving oncogenic progression.Mitochondrial dysfunction in tumors is highly heterogeneous,influencing disease phenotypes and treatment responses across cancer types.Within the tumor microenvironment,mitochondria profoundly impact immune responses by modulating T-cell survival and function,macrophage polarization,NK cell cytotoxicity,and neutrophil activation.They also mediate stromal cell functions,particularly in cancer-associated fibroblasts and tumor endothelial cells.Although targeting mitochondrial function represents a promising therapeutic strategy,mitochondrial heterogeneity and adaptive resistance mechanisms complicate interventional approaches.Advances in mitochondrial genome editing,proteomics,and circulating mitochondrial DNA analysis have enhanced tumor diagnostic precision.This review synthesizes the developmental landscape of mitochondrial research in cancer,comprehensively summarizing mitochondrial structural dynamics,metabolic plasticity,signaling networks,and interactions with the tumor microenvironment.Finally,we discuss the translational challenges in developing effective mitochondria-based cancer interventions. 展开更多
关键词 adaptive responses oxidative phosphorylation mitochondrial metabolism MITOCHONDRIA tumor development epigene cancer therapeutic innovation tricarboxylic acid cycle
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