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1.
癌症是当今威胁人类健康的主要疾病之一。近年来提出的近红外光介导的光热治疗,能够对肿瘤组织进行定点清除并且对正常组织具有较低的毒副作用,为肿瘤的治疗提供了新的方法。开发具有良好生物相容性的高效光热偶联剂是发展光热治疗的首要条件。随着纳米技术的飞速发展,一些金属纳米结构由于具有独特的光学特性作为光热偶联剂被广泛应用到肿瘤的光热治疗中。然而,成本高昂、制备过程繁琐以及光热稳定性较差等不足,限制了这些纳米材料的进一步应用。最新报道的新型光热偶联剂半导体硫化铜纳米粒子(copper sulfide nanoparticles,CuS NPs),由于其具有制备工艺简单、成本低廉、突出的光热稳定性和良好的生物相容性等优势,成为了当今纳米医学领域研究的热点。本文主要综述了CuS纳米粒子在肿瘤光热治疗和影像诊断方面的应用研究,并对CuS纳米粒子在生物医学领域应用中存在的问题和未来的研究方向进行了展望。  相似文献   

2.
硫化铜是一种二价铜的硫化物,可以作为半导体材料,化学式为CuS,呈黑褐色,溶解度极低。硫化铜纳米粒子(Copper sulfide nanoparticles, CuS NPs)是纳米尺度大小的硫化铜。近年来,CuS NPs因其结构的可塑性,良好的光热稳定性、生物相容性、突出的光热及光声转换性能,成为了当今纳米材料医学领域的研究热点,在肿瘤诊断和治疗领域中引起了广泛关注。CuS NPs本身可通过介质鳌合金属离子合成多功能纳米粒子,实现肿瘤多模式诊断,并且在光热治疗研究中体现出突出的治疗效果。本文综述了近几年CuS NPs在肿瘤诊断与治疗方面的研究进展,总结肿瘤治疗中的应用研究方法,对CuS NPs在生物医学领域应用中存在的问题进行分析,为解决实际操作过程所遇到的问题提供参考。  相似文献   

3.
纳米技术在生物医学的进展使其在肿瘤的诊治中应用日益广泛。荧光纳米粒子中的量子点(Quantum Dots),具备光学成像特性在肿瘤中应用中显示出独特的优势。其作为一种荧光半导体纳米粒子,具有荧光强度高、稳定性强、激发波谱宽、发射波谱窄等光学特性。同时,它可以结合其他功能基团,包括靶向模式、治疗因素和成像探针,为临床肿瘤诊断和治疗提供了新的潜力。本文就量子点的类型和特点及量子点的肿瘤体外和体内成像进行综述。  相似文献   

4.
金纳米棒具有独特的光学性质、表面易修饰性、较低的生物毒性和良好的生物相容性,因而在成像、光热治疗和药物载带等方面具有极高的潜在应用价值.本文综述了典型的金纳米棒表面修饰方法及其在生物成像、光热治疗和药物治疗中的应用,重点阐述了通过金纳米棒同时实现肿瘤诊断和治疗相结合的研究进展.  相似文献   

5.
IX型分泌系统(Type IX Secretion System,T9SS)是一种最新发现的存在于许多革兰氏阴性细菌中的分泌系统。T9SS参与细菌的毒力和滑行运动及复杂生物聚合物的降解过程。近年来,与T9SS相关的研究一直都是微生物学领域关注的热点。本文就T9SS的发现、组成与结构、分泌机制及调控机制等方面的研究进展进行综述,以期为进一步解析细菌的T9SS提供新的思路。  相似文献   

6.
肿瘤干细胞(cancer stem cells,CSCs)学说的成熟发展和研究成为当前肿瘤治疗研究的热点之一,因其特殊的生物学特性在肿瘤防治中起重要作用。以CSCs为靶点为肿瘤治疗开辟了一条新思路。传统的治疗不能有效靶向CSC,开发针对CSC靶向治疗的新方法,将对肿瘤的耐药、复发、转移具有革新意义。  相似文献   

7.
纳米金颗粒以其优越的理化性质在医学领域发挥独特的作用.近年来越来越多的研究证实了纳米金在肿瘤早期诊断和治疗方面方面有重要作用,尤其是纳米金正被逐步应用肿瘤成像和治疗领域.本文从纳米金的性质,在肿瘤成像和放射治疗方面的应用进展等方面作一综述.  相似文献   

8.
9.
癌症是导致人类死亡的主要原因之一。尽管现代医学在癌症治疗方面取得了重大进展,但由于癌症的异质性、耐药性和治疗副作用等问题,传统治疗手段仍存在局限性。随着科学技术的不断发展,细菌治疗在肿瘤治疗领域展现出巨大潜力。细菌因其生存特性具有天然的肿瘤靶向能力,并含有大量免疫激活物质,可调节肿瘤微环境并激活免疫系统以达到杀伤肿瘤的目的。部分细菌还能通过多种途径直接杀伤肿瘤细胞并抑制肿瘤血管生成。此外,科学家们在深入探索过程中发现,细菌联合放疗、化疗和免疫治疗等方法逐渐成为细菌治疗的主流策略。并可根据临床需求,将外源性基因导入细菌以发挥特定功能。细菌疗法通过与多种治疗方式联用来克服各自的治疗缺陷,提高肿瘤的治疗效果并降低其毒性副作用。从细菌治疗的基本原理、常用于肿瘤治疗的细菌种类、细菌治疗的优化策略及临床试验和案例等方面进行综述。希望通过充分发挥细菌的治疗潜力,为癌症患者提供更加有效的治疗手段。  相似文献   

10.
目的:建立一种可以同时实现显像诊断与主动靶向到肿瘤部位进行治疗的纳米药物模型。方法:包载了1,1'-二十八烷基-3,3,3',3'-四甲基吲哚三碳花青碘(1,1'-dioctadecyl-3,3,3',3'-tetramethylindotricarbocyanine iodide, Di R)荧光染料的聚乳酸-羟基乙酸共聚物(Polylactic-co-glycolic acid, PLGA)纳米粒表面被金属离子与酚羟基络合形成的网状结构涂布后可稳定连接在巨噬细胞表面,Di R可以在近红外激光下实现荧光成像,并经波长为808 nm的近红外激光器以2 W/cm2功率照射,产生光热作用。结果:构建了粒径在100 nm左右的包载了Di R的PLGA纳米粒,表面涂布金属多酚网状结构后,纳米粒连接到巨噬细胞表面,Di R发挥既可荧光成像,经808 nm激光照射后又可高效升温至46℃以上,使用CCK8试剂检测证明此种连接了纳米粒的功能化细胞(Functional Cell)发挥光热作用后可杀死近70%的小鼠乳腺癌细胞4T1。结论:成功建立了一种基于巨噬细胞递送的诊疗一体化系统,将荧光成像与光热治疗有机结合到一起,达到有效杀伤肿瘤细胞的功效。  相似文献   

11.
Cell migration can be principally viewed as a chain of well-orchestrated morphological events that lead to dynamic reshaping of the cell body. However, behind the scene of such a “morphological theater” there are very complex, interrelated molecular and physiological processes that drive the cell movement. Among them, ion transport and pH regulation play a key role, with carbonic anhydrase IX (CA IX) emerging as one of the important “molecular actors.” CA IX is a highly active cell surface enzyme expressed in a broad range of solid tumors in response to hypoxia and explored as a clinically useful biomarker of hypoxia and as a therapeutic target. Its biological role is to protect tumor cells from hypoxia and acidosis in the tumor microenvironment. The study published recently by our group showed that CA IX actively contributes to cell migration and invasion. For the first time, we demonstrated CA IX accumulation in lamellipodia of migrating cells and its direct in situ interaction with bicarbonate transporters. Our findings indicate that tumor cells need CA IX not only as a pro-survival factor in hypoxia and acidosis, but also as a pro-migratory component of the cellular apparatus driving epithelial-mesenchymal transition.  相似文献   

12.
Abstract

Among the diagnostic techniques for the identification of tumour biomarkers, the liquid biopsy is considered one that offers future research on precision diagnosis and treatment of tumours in a non-invasive manner. The approach consists of isolating tumor-derived components, such as circulating tumour cells (CTC), tumour cell-free DNA (ctDNA), and extracellular vesicles (EVs), from the patient peripheral blood fluids. These elements constitute a source of genomic and proteomic information for cancer treatment. Within the tumour-derived components of the body fluids, the enzyme indicated with the acronym CA IX and belonging to the superfamily of carbonic anhydrases (CA, EC 4.2.1.1) is a promising aspirant for checking tumours. CA IX is a transmembrane-CA isoform that is strongly overexpressed in many cancers being not much diffused in healthy tissues except the gastrointestinal tract. Here, it is summarised the role of CA IX as tumour-associated protein and its putative relationship in liquid biopsyfor diagnosing and monitoring cancer progression.  相似文献   

13.
Extracellular acidification, a mandatory feature of several malignancies, has been mainly correlated with metabolic reprogramming of tumor cells toward Warburg metabolism, as well as to the expression of carbonic anydrases or proton pumps by malignant tumor cells. We report herein that for aggressive prostate carcinoma, acknowledged to be reprogrammed toward an anabolic phenotype and to upload lactate to drive proliferation, extracellular acidification is mainly mediated by stromal cells engaged in a molecular cross-talk circuitry with cancer cells. Indeed, cancer-associated fibroblasts, upon their activation by cancer delivered soluble factors, rapidly express carbonic anhydrase IX (CA IX). While expression of CAIX in cancer cells has already been correlated with poor prognosis in various human tumors, the novelty of our findings is the upregulation of CAIX in stromal cells upon activation. The de novo expression of CA IX, which is not addicted to hypoxic conditions, is driven by redox-based stabilization of hypoxia-inducible factor-1. Extracellular acidification due to carbonic anhydrase IX is mandatory to elicit activation of stromal fibroblasts delivered metalloprotease-2 and -9, driving in cancer cells the epithelial-mesenchymal transition epigenetic program, a key event associated with increased motility, survival and stemness. Both genetic silencing and pharmacological inhibition of CA IX (with sulfonamide/sulfamides potent inhibitors) or metalloprotease-9 are sufficient to impede epithelial-mesenchymal transition and invasiveness of prostate cancer cells induced by contact with cancer-associated fibroblasts. We also confirmed in vivo the upstream hierarchical role of stromal CA IX to drive successful metastatic spread of prostate carcinoma cells. These data include stromal cells, as cancer-associated fibroblasts as ideal targets for carbonic anhydrase IX-directed anticancer therapies.  相似文献   

14.
Carbonic anhydrase (CA) enzymes have been shown to play an important role in ion transport and in pH regulation in several organisms. Despite this information and the wealth of knowledge regarding the significance of CA enzymes, few studies have been reported about bee CA enzymes and the hazardous effects of chemicals. Using Apis mellifera as a model, this study aimed to determine the risk of pesticides on Apis mellifera Carbonic anhydrase enzyme (Am CA). CA was initially purified from Apis mellifera spermatheca for the first time in the literature. The enzyme was purified with an overall purification of ~35-fold with a molecular weight of ~32?kDa. The enzyme was then exposed to pesticides, including tebuconazole, propoxur, carbaryl, carbofuran, simazine and atrazine. The six pesticides dose-dependently inhibited in vitro AmCA activity at low micromolar concentrations. IC50 values for the pesticides were 0.0030, 0.0321, 0.0031, 0.0087, 0.0273 and 0.0165?μM, respectively. The AmCA inhibition mechanism of these compounds is unknown at this moment.  相似文献   

15.
16.
We report the synthesis and characterisation of a novel series of triazole benzenesulfonamide derivatives, which incorporate the general pharmacophore associated with carbonic anhydrase (CA, EC 4.2.1.1) inhibitors. The synthesised compounds were tested in vitro against four human carbonic anhydrase (hCA, EC 4.2.1.1) isozymes, hCA I, hCA II, hCA IV and hCA IX. The obtained results showed that the tumour-associated hCA IX was the most sensitive to inhibition with the synthesised derivatives, with the triazolo-pyridine benzenesulfonamides 14, 16 and 17 being the most effective inhibitors. Some selected compounds were chosen for a single dose anti-proliferative activity testing against a panel of 57 human tumour cell lines and show some anti-proliferative activity ex vivo.  相似文献   

17.
Carbonic anhydrase II electrophoretic patterns were investigated in 3113 animals belonging to 12 genera and 24 species of New World primates. Polymorphism was detected in 13 species. A total of 24 different alleles was postulated to explain the variability found; the genusAotus showed the highest (eight) number of such alleles. Three genera of the family Callitrichidae (Callithrix, Saguinus, andCebuella) presented five alleles that were not found among the Cebidae. Important markers at the generic level were observed inCallicebus (CA2 *6 andCA2 *12),Cebus (CA2 *10, CA2*16, andCA2 *21), andAotus (CA2*3, CA2*4, CA2*5, CA2*9, CA2*15, CA2*17, CA2*22, CA2*23). CA2*13 seems to be the most common allele among the Cebidae; six genera of this family showed frequencies higher than 70% of it.  相似文献   

18.
The activity and cellular localization of carbonic anhydrase (CA) in two alkaliphilic anaerobes growing in soda lakes at pH 9–10 were studied. CA activity in the cell extracts of the acetogenic bacterium Natroniella acetigena was comparable to that of neutrophilic acetogens. Hydrogenotrophically grown cells of Desulfonatronum lacustre exhibited higher CA activity compared to the cells grown on medium with formate. High CA activity in the cytoplasmic fraction and the absence of high activity in the extracellular fraction were demonstrated. We propose that the cytoplasmic CA in alkaliphilic sulfate-reducers participates in conversion of bicarbonate to CO2, which is reduced in the cell to acetate via the acetyl-CoA pathway.  相似文献   

19.
Nonaqueous fractionation of leaves of the cotton plant suggested that carbonic anhydrase was associated with the chloroplasts. Activity of this enzyme in aqueous extracts prepared in media containing no reductants was stable at 4°. Response to sulfhydryl reagents varied. The results indicated that thiol groups, necessary for the activity of the enzyme, were partially protected from oxidation.  相似文献   

20.
Carbonic anhydrase (CA, EC 4.2.1.1) catalyses the first reaction in the C4 photosynthetic pathway, the conversion of atmospheric CO2 to bicarbonate in the mesophyll cytosol. To examine the importance of the enzyme to the functioning of the C4 photosynthetic pathway, Flaveria bidentis (L.) Kuntze, a C4 dicot, was genetically transformed with an antisense construct in which the cDNA encoding a putative cytosolic CA (CA3) was placed under the control of a constitutive promoter. Some of the primary transformants had impaired CO2 assimilation rates and required high CO2 for growth. The T1 progeny of four primary transformants were used to examine the quantitative relationship between leaf CA activity and CO2 assimilation rate. CA activity was determined in leaf extracts with a mass spectrometric technique that measured the rate of 18O exchange from doubly labelled 13C18O2. Steady‐state CO2 assimilation rates were unaffected by a decrease in CA activity until CA activity was less than 20% of wild type when they decreased steeply. Transformants with less than 10% of wild‐type CA activity had very low CO2 assimilation rates and grew poorly at ambient CO2 partial pressure. Reduction in CA activity also increased the CO2 partial pressure required to saturate CO2 assimilation rates. The present data show that CA activity is essential for the functioning of the C4 photosynthetic pathway.  相似文献   

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