Opposite angiogenic outcome of curcumin against ischemia and Lewis lung cancer models:in silico,in v

来源 :第八届国际分子模拟与信息技术应用学术会议 | 被引量 : 0次 | 上传用户:scholar165
下载到本地 , 更方便阅读
声明 : 本文档内容版权归属内容提供方 , 如果您对本文有版权争议 , 可与客服联系进行内容授权或下架
论文部分内容阅读
  The aim of this study was to investigate the angiogenic effects of curcumin on an ischemia and lung cancer model.To induce ischemia combined with lung cancer models,unilateral femoral arteries of C57BL/6 mice were disconnected on one side of the mouse and Lewis lung carcinoma(LLC)cells were xenografted on the opposite side.Angiogenic effects and underlying mechanisms associated with curcumin were investigated.Molecular larget(s),signaling cascades and binding affinities were delected by Western blot,two-dimensional gel electrophoresis(2-DE),computer simulations and surface plasmon resonance(SPR)techniques.Curcumin promoted post-ischemic blood recirculation and suppressed lung cancer progression in inbred C57BL/6 mice via regulation of the HIF1α/mTQR/VECF/VEGFR cascade oppositely.Inflammatory stimulation induced by neutrophil elaslase(NE)promoted angiogenesis in lung cancer tissues,but these changes were reversed by curuimin through directly reducing NE secretion and stimulating α1-antitrypsin(α1-AT)and insulin receptor substrate-1(IRS-1)production.Meanwhile,curcumin dosc-dependently influenced endothelial cells(EC)tube formation and thicken embryo chorioallantoic membiane(CAM)neovasctilarization.Curcumin had opposite effects on blood vessel regeneration under physiological and pathological angiogenesis,which was effected through negative or positive regulation of the HIF1α/mTOR/VEGF/VEGFR cascade.Curcumin had the promise as a new treatment modality for both ischemic conditions and lung cancer simultaneously in the clinic.
其他文献
A Chinese natural product,jatrorrhizine hydrochloride(JH),exhibited a potent inhibitory effect toward neuraminidase of the H7N9(N9)avian influenza virus.The interaction between JH and N9 was modeled u
会议
A series of novel 2-(1,3-diaryl-4,5-dihydro-1H-pyrazol-5-yl)phenol derivatives(C1-C24)have been synthesized.The B-Raf inhibitory activity and anti-proliferation activity of these compounds have been t
会议
Cytochrome P450 2E1 is widely known for its ability to oxidize both low molecular weight xenobiotics and endogenous fatty acids(e.g.,arachidonic acid(AA)).In this study,we investigated the structural
Background: Trichinellosis is a re-emerging infectious disease,caused by Trichinella spp.Cathepsin F belongs to cysteine protease that is a major virulence factor for parasitic helminths,and it may be
Protein electrospray ionization(ESI)mass spectrometry(MS)-based techniques are widely used to provide insight into structural proteomics under the assumption that non-covalent protein complexes being
会议
The interaction between barrier-to-autointegration factor dimer(BAF2)and LEM domain of emerin(EmLEM was studied by molecular simulation methods.Nonspecific fragment of double-strand DNA molecule was d
Histone deacetylase inhibitors(HDIs)are an increasingly important class of cancer-targeting agent.Two kinds of small molecule histone deacetylase inhibitors,mainly employing the motifs of the two know
会议
The connection between inflammation and tumourigenesis has been well established.However,the detailed molecular mechanism underlying inflammation-associated tumourigenesis remains unknown because this
会议
Traditional Chinese medicine(TCM)is a multi-component and multi-target agent and could treat complex diseases in a holistic way,especially infection diseases.However,the underlying pharmacology remain
会议
Metronidazole-sulfonamide derivatives 4a-4l,a new class of human carbonic anhydrase inhibitors(hCA),were designed,synthesized,isolated,and evaluated for their ability to inhibit the enzymatic activity
会议