23 research outputs found
HIF-1Ī± effects on angiogenic potential in human small cell lung carcinoma
<p>Abstract</p> <p>Background</p> <p>Hypoxia-inducible factor-1 alpha (HIF-1Ī±) maybe an important regulatory factor for angiogenesis of small cell lung cancer (SCLC). Our study aimed to investigate the effect of HIF-1Ī± on angiogenic potential of SCLC including two points: One is the effect of HIF-1Ī± on the angiogenesis of SCLC <it>in vivo</it>. The other is the regulation of angiogenic genes by HIF-1Ī± <it>in vitro </it>and <it>in vivo</it>.</p> <p>Methods</p> <p><it>In vivo </it>we used an alternative method to study the effect of HIF-1a on angiogenic potential of SCLC by buliding NCI-H446 cell transplantation tumor on the chick embryo chorioallantoic membrane (CAM) surface. <it>In vitro </it>we used microarray to screen out the angiogenic genes regulated by HIF-1a and tested their expression level in CAM transplantation tumor by RT-PCR and Western-blot analysis.</p> <p>Results</p> <p><it>In vivo </it>angiogenic response surrounding the SCLC transplantation tumors in chick embryo chorioallantoic membrane (CAM) was promoted after exogenous HIF-1Ī± transduction (p < 0.05). <it>In vitro </it>the changes of angiogenic genes expression induced by HIF-1Ī± in NCI-H446 cells were analyzed by cDNA microarray experiments. HIF-1Ī± upregulated the expression of angiogenic genes VEGF-A, TNFAIP6, PDGFC, FN1, MMP28, MMP14 to 6.76-, 6.69-, 2.26-, 2.31-, 4.39-, 2.97- fold respectively and glycolytic genes GLUT1, GLUT2 to2.98-, 3.74- fold respectively. In addition, the expression of these angiogenic factors were also upregulated by HIF-1Ī± in the transplantion tumors in CAM as RT-PCR and Western-blot analysis indicated.</p> <p>Conclusions</p> <p>These results indicated that HIF-1Ī± may enhance the angiogenic potential of SCLC by regulating some angiogenic genes such as VEGF-A, MMP28 etc. Therefore, HIF-1Ī± may be a potential target for the gene targeted therapy of SCLC.</p
Role of poly (ADP-ribose) polymerase-1 and NF-kappaB as potential risk factor in the development of non-small cell lung cancer in Chinese individuals
LKB1 suppression promotes cardiomyocyte regeneration via LKB1-AMPK-YAP axis
The regenerative potential of cardiomyocytes in adult mammals is limited. Previous studies reported that cardiomyocyte proliferation is suppressed by AMP-activated protein kinase (AMPK). The role of liver kinase B1 (LKB1), as the major upstream kinase for AMPK, on cardiomyocyte proliferation is unclear. In this study, we found that the LKB1 levels rapidly increased after birth. With loss- and gain-of-function study, our data demonstrated that LKB1 levels negatively correlate with cardiomyocyte proliferation. We next identified Yes-associated protein (YAP) as the downstream effector of LKB1 using high-throughput RNA sequencing. Our results also demonstrated that AMPK plays an essential role in Lkb1 knockdown-induced cardiomyocyte proliferation. Importantly, deactivated AMPK abolished the LKB1-mediated regulation of YAP nuclear translocation and cardiomyocyte proliferation. Thus, our findings suggested the role of LKB1-AMPK-YAP axis during cardiomyocyte proliferation, which could be used as a potential target for inducing cardiac regeneration after injury
Role of poly (ADP-ribose) polymerase-1 and NF-kappaB as potential risk factor in the development of non-small cell lung cancer in Chinese individuals
The objective of this study was to evaluate the role of poly (ADP-ribose) polymerase-1 (PARP-1) and NF-kappaB as potential risk factor in the development of non-small cell lung cancer in Chinese individuals (n=110) of either gender aged <65 years. Healthy Chinese individuals (n=110) were included as control. Polymerase chain reaction was used to determine the role of PART-1 and NF-kappaB using plasma sample. The individuals with the GA genotype and carrier of G allele were at high-risk of non-small cell lung cancer. There was involvement of dL/is of the NF-kappaB in non-small cell lung cancer. Our study result suggests that the PARP-1 and NF-kappaB play an important role in development of non-small cell lung cancer in China
Long Noncoding RNA Ahit Protects Against Cardiac Hypertrophy Through SUZ12 (Suppressor of Zeste 12 Protein Homolog)-Mediated Downregulation of MEF2A (Myocyte Enhancer Factor 2A)
Down-regulation of AMPK/PPARĪ“ signalling promotes endoplasmic reticulum stress-induced endothelial dysfunction in adult rat offspring exposed to maternal diabetes
AIMS: Exposure to maternal diabetes is associated with increased prevalence of hypertension in the offspring. The mechanisms underlying the prenatal programming of hypertension remain unclear. Because endoplasmic reticulum (ER) stress plays a key role in vascular endothelial dysfunction in hypertension, we investigated whether aberrant ER stress causes endothelial dysfunction and high blood pressure in the offspring of dams with diabetes. METHODS AND RESULTS: Pregnant Sprague-Dawley rats were intraperitoneally injected with streptozotocin (35 mg/kg) or citrate buffer at Day 0 of gestation. Compared with control mother offspring (CMO), the diabetic mother offspring (DMO) had higher blood pressure and impaired endothelium-dependent relaxation in mesenteric arteries, accompanied by decreased AMPK phosphorylation and PPARĪ“ expression, increased ER stress markers, and reactive oxygen species (ROS) levels. The inhibition of ER stress reversed these aberrant changes in DMO. Ex vivo treatment of mesenteric arteries with an AMPK agonist (A769662) or a PPARĪ“ agonist (GW1516) improved the impaired EDR in DMO and reversed the tunicamycin-induced ER stress, ROS production, and EDR impairment in mesenteric arteries from CMO. The effects of A769662 were abolished by co-treatment with GSK0660 (PPARĪ“ antagonist), whereas the effects of GW1516 were unaffected by Compound C (AMPK inhibitor). CONCLUSION: These results suggest an abnormal foetal programming of vascular endothelial function in offspring of rats with maternal diabetes that is associated with increased ER stress, which can be ascribed to down-regulation of AMPK/PPARĪ“ signalling cascade
CāC Coupling on Single-Atom-Based Heterogeneous Catalyst
Compared
to homogeneous catalysis, heterogeneous catalysis allows
for ready separation of products from the catalyst and thus reuse
of the catalyst. CāC coupling is typically performed on a molecular
catalyst which is mixed with reactants in liquid phase during catalysis.
This homogeneous mixing at a molecular level in the same phase makes
separation of the molecular catalyst extremely challenging and costly.
Here we demonstrated that a TiO<sub>2</sub>-based nanoparticle catalyst
anchoring singly dispersed Pd atoms (Pd<sub>1</sub>/TiO<sub>2</sub>) is selective and highly active for more than 10 Sonogashira CāC
coupling reactions (Rī¼CH + Rā²X ā Rī¼Rā²;
X = Br, I; Rā² = aryl or vinyl). The coupling between iodobenzene
and phenylacetylene on Pd<sub>1</sub>/TiO<sub>2</sub> exhibits a turnover
rate of 51.0 diphenylacetylene molecules per anchored Pd atom per
minute at 60 Ā°C, with a low apparent activation barrier of 28.9
kJ/mol and no cost of catalyst separation. DFT calculations suggest
that the single Pd atom bonded to surface lattice oxygen atoms of
TiO<sub>2</sub> acts as a site to dissociatively chemisorb iodobenzene
to generate an intermediate phenyl, which then couples with phenylacetylenyl
bound to a surface oxygen atom. This coupling of phenyl adsorbed on
Pd<sub>1</sub> and phenylacetylenyl bound to O<sub>ad</sub> of TiO<sub>2</sub> forms the product molecule, diphenylacetylene
Progesterone, via yes-associated protein, promotes cardiomyocyte proliferation and cardiac repair.
Prenatal Lipopolysaccharides Exposure Induces Transgenerational Inheritance of Hypertension
BACKGROUND: Adverse environmental exposure during the prenatal period can lead to diseases in the offspring, including hypertension. Whether or not the hypertensive phenotype can be transgenerationally transmitted is not known. METHODS: Pregnant Sprague Dawley rats were intraperitoneally injected with lipopolysaccharide (LPS) on gestation days 6, 8, 10, and 12 to generate the prenatal LPS exposure model. Blood pressure was monitored by both telemetry and tail-cuff method. RNA sequencing was performed to analyze transcriptome alteration in the kidney of the third generation. Tempol and spironolactone were used to test the potential prevention and therapeutic effect of targeting reactive oxygen species and mineralocorticoid receptor signaling, respectively. Molecular biological experiments were performed to illustrate the mechanism of epigenetic and transcription regulation. RESULTS: Prenatal LPS exposure can impair the ability to excrete a salt load and induce hypertension from the first to the third generations, with the fourth and fifth generations, inducing salt-sensitive hypertension. Compared with control pups, the transcriptome in the kidney of the hypertensive third-generation prenatal LPS-exposed offspring have upregulation of the Ras-related C3 botulinum toxin substrate 1 () gene and activation of mineralocorticoid receptor signaling. Furthermore, we found that LPS exposure during pregnancy triggered oxidative stress that upregulated KDM3B (histone lysine demethylase 3B) in the oocytes of first-generation female rats, leading to an inheritable low level of H3K9me2 (histone H3 lysine 9 dimethylation), resulting in the transgenerational upregulation of . Based on these findings, we treated the LPS-exposed pregnant rats with the reactive oxygen species scavenger, tempol, which successfully prevented hypertension in the first-generation offspring and the transgenerational inheritance of hypertension. CONCLUSIONS: These findings show that adverse prenatal exposure induces transgenerational hypertension through an epigenetic-regulated mechanism and identify potentially preventive and therapeutic strategies for hypertension