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1.
Front Oncol ; 11: 650383, 2021.
Article in English | MEDLINE | ID: mdl-33816306

ABSTRACT

N6-methyladenosine (m6A) is the most common post-transcriptional modification of RNA in eukaryotes, which has been demonstrated to play important roles in various cancers. YTHDF1 acts as a crucial m6A "reader" and regulates the fate of m6A modified mRNA. However, its role in cervical cancer remains unknown. In this study, we showed that YTHDF1 was highly expressed in cervical cancer, and was closely associated with the poor prognosis of cervical cancer patients. YTHDF1 knockdown suppressed the growth, migration and invasion, and induced apoptosis of cervical cancer cells. Moreover, YTHDF1 knockdown inhibited tumorigenesis of cervical cancer cells in vivo. Through combined on-line data analysis of RIP-seq, meRIP-seq and Ribo-seq upon YTHDF1 knockdown, RANBP2 was identified as the key target of YTHDF1 in cervical cancer cells. YTHDF1 regulated RANBP2 translation in an m6A-dependent manner without effect on its mRNA expression. RANBP2 potentiated the growth, migration and invasion of cervical cancer cells. Our study demonstrated the oncogenic role of YTHDF1 in cervical cancer by regulating RANBP2 expression and YTHDF1 represents a potential target for cervical cancer therapy.

2.
Biosci Rep ; 40(2)2020 02 28.
Article in English | MEDLINE | ID: mdl-31994698

ABSTRACT

BACKGROUND: Spinal cord injury (SCI) is a challenge worldwide, but there are no effective treatments or therapeutic methods in the clinic. Recent studies have shown that type I arginase (Arginase1, Arg1) is closely associated with the treatment of SCI. The classical treatment for SCI involves filling the local area of SCI with activated M2a macrophages to allow the repair and regeneration of some synapses, but the specific mechanism of action of Arg1 is not clear. METHOD: In the present study, we first induced the polarization of RAW264.7 macrophages to M2a-type cells using IL-4 and constructed an Arg1 knockout cell line through the use of shRNA; we used these cells to treat a rat model of SCI. Finally, the present study explored the mechanism and pathway by which Arginase 1 regulates spinal repair by immunoblotting and immunohistochemistry. RESULT: Suspended M2a (Arg1-/+) macrophages were transplanted into the injury site in a rat model of contusion SCI. Compared with the model group and the shArg1 group, the shScramble (shSc) group exhibited higher Basso, Beattie, Bresnahan motor function scores, more compact structures and more Nissl bodies. Immunohistochemical results showed that the shSc group expressed higher levels of NeuN (a neuronal marker) and tau (an axonal marker), as well as the up-regulation of Cdc42, N-WASP, Arp2/3 and tau, as determined by Western blot. CONCLUSION: The study found that the polarization of M2a macrophages promoted the expression of Arginase 1, which restored axonal regeneration, promoted axonal regeneration, and promoted the structural and functional recovery of the contused spinal cord.


Subject(s)
Arginase/metabolism , Axons/pathology , Macrophage Activation , Macrophages/transplantation , Nerve Regeneration , Spinal Cord Injuries/therapy , Spinal Cord/physiopathology , Actin-Related Protein 2/metabolism , Animals , Arginase/genetics , Axons/metabolism , Disease Models, Animal , Female , Interleukin-4/pharmacology , Macrophage Activation/drug effects , Macrophages/drug effects , Macrophages/enzymology , Male , Mice , Motor Activity , RAW 264.7 Cells , Rats, Sprague-Dawley , Recovery of Function , Signal Transduction , Spinal Cord/metabolism , Spinal Cord/pathology , Spinal Cord Injuries/metabolism , Spinal Cord Injuries/pathology , Spinal Cord Injuries/physiopathology , Wiskott-Aldrich Syndrome Protein, Neuronal/metabolism , cdc42 GTP-Binding Protein/metabolism , tau Proteins/metabolism
3.
Springerplus ; 5(1): 1497, 2016.
Article in English | MEDLINE | ID: mdl-27652070

ABSTRACT

The development of high-energy weapons could increase the velocity of projectiles to well over 1000 m/s. The nature of the injuries caused by the ballistic impact of projectiles at velocities much faster than 1000 m/s is unclear. This study characterizes the mechanical and biochemical alterations caused by high-speed ballistic impact generated by spherical steel ball to the hind limbs of the pig. That the local and distal injuries caused by hypervelocity ballistic impact to the living body are also identified. It is showed that the severity of the injury was positively correlated with the velocity of the projectile. And 4000 m/s seems to be the critical velocity for the 5.6 mm spherical steel ball, which would cause severe damage to either local or distal organs, as below that speed the projectile penetrated the body while above that speed it caused severe damage to the body. In addition, vaporization prevented the projectile from penetrating the body and the consequent pressure wave seems to be the causal factor for the distant damage.

4.
Technol Health Care ; 23 Suppl 1: S61-70, 2015.
Article in English | MEDLINE | ID: mdl-26410330

ABSTRACT

To establish a finite element (FE) model of the pig head for simulating firearm wounds. An experimental study was carried out by measuring impact load parameters from 17 fresh pig heads that were shot at the right part of cranium by a standard 7.62 mm M43 bullet. FE analysis was executed through the LS-DYNA code under impact loads similar to those obtained from the experimental study. The residual velocity, the transferred energy from the bullet to the cranium, and the surface area of the entrance showed no statistical differences between the FE simulation and the experimental study. However, the mean surface area of the exit wounds was significantly larger than that of the entrance wounds in the experimental and FE study. Although the results of FE analysis corresponded with the experiment study, FE analysis further revealed that the stress zones were mainly located at the impact region of the cranium, mainly located in occipital lobe, frontal lobe and skull base of brain, with a lower speed of stress distribution. The FE model was appropriate and conformed to the basic principles of wound ballistics.


Subject(s)
Finite Element Analysis , Head , Wounds, Gunshot/physiopathology , Animals , Biomechanical Phenomena , Computer Simulation , Models, Biological , Swine
5.
Int J Clin Exp Pathol ; 7(4): 1724-32, 2014.
Article in English | MEDLINE | ID: mdl-24817970

ABSTRACT

BACKGROUND: Free radical-induced oxidative damage of the brain has been implicated in a number of psychiatric disorders, including post-traumatic stress disorder (PTSD). Catalase (CAT) is a major antioxidant enzyme and a number of polymorphisms in CAT have been shown to be associated with several diseases, including hypertension, diabetes mellitus, Alzheimer's disease, and vitiligo. The aim of this study was to evaluate the association of CAT gene polymorphisms with PTSD in a case-control study. MATERIALS AND METHODS: A total of 460 unrelated adult Chinese Han adults, including 287 healthy volunteers and 173 patients with PTSD. Six tag single-nucleotide polymorphisms (tSNPs) were selected from the entire CAT gene through construction of haplotype bins, and they were genotyped using an improved multiplex ligation detection reaction (iMLDR) technique. Allelic frequencies and clinical characteristics were compared in two independent Chinese Han populations. RESULTS: Six tag SNPs were identified in the Chinese Han population and all were common SNPs. However, we could detect no evidence of genetic association between six tag SNPs in the CAT gene and PTSD in the Chinese Han population. CONCLUSIONS: This result suggests that six tag SNPs of the CAT gene may not be associated with PTSD, and that CAT gene might not influence the development of PTSD in patients following exposure to a traumatic event, also may be the sample sizes too small to allow a meaningful test.


Subject(s)
Asian People/genetics , Catalase/genetics , Polymorphism, Single Nucleotide/genetics , Stress Disorders, Post-Traumatic/genetics , Adolescent , Adult , Case-Control Studies , China/epidemiology , Female , Gene Frequency/genetics , Genetic Predisposition to Disease/genetics , Haplotypes/genetics , Humans , Male , Middle Aged , Stress Disorders, Post-Traumatic/epidemiology , Young Adult
6.
PLoS One ; 8(12): e81310, 2013.
Article in English | MEDLINE | ID: mdl-24358110

ABSTRACT

BACKGROUND: Because the characteristics of blast waves in water are different from those in air and because kinetic energy is liberated by a pressure wave at the water-air interface, thoracic injuries from mine blasts in shoals may be serious. The aim of the present study was to investigate the characteristics and mechanisms of cardiopulmonary injury caused by mine blasts in shoals. METHODS: To study the characteristics of cardiopulmonary injury, 56 animals were divided randomly into three experimental groups (12 animals in the sham group, 22 animals in the land group and 22 animals in the shoal group). To examine the biomechanics of injury, 20 animals were divided randomly into the land group and the shoal group. In the experimental model, the water surface was at the level of the rabbit's xiphoid process, and paper electric detonators (600 mg RDX) were used to simulate mines. Electrocardiography and echocardiography were conducted, and arterial blood gases, serum levels of cardiac troponin I and creatine kinase-MB and other physiologic parameters were measured over a 12-hour period after detonation. Pressures in the thorax and abdomen and the acceleration of the thorax were measured. CONCLUSION: The results indicate that severe cardiopulmonary injury and dysfunction occur following exposure to mine blasts in shoals. Therefore, the mechanisms of cardiopulmonary injury may result from shear waves that produce strain at the water-air interface. Another mechanism of injury includes the propagation of the shock wave from the planta to the thorax, which causes a much higher peak overpressure in the abdomen than in the thorax; as a result, the abdominal organs and diaphragm are thrust into the thorax, damaging the lungs and heart.


Subject(s)
Blast Injuries/physiopathology , Explosions , Heart Injuries/physiopathology , Lung Injury/physiopathology , Thoracic Injuries/physiopathology , Animals , Disease Models, Animal , Rabbits
7.
Int J Clin Exp Pathol ; 6(6): 1142-9, 2013.
Article in English | MEDLINE | ID: mdl-23696934

ABSTRACT

Dopamine D2 receptor is involved in reward-mediating mesocorticolimbic pathways. It plays an important role in major depressive disorder (MDD). Three gene polymorphisms Taq1A, C957T and -141C ins/del, were identified in the DRD2 gene among the Western population. These variants in the DRD2 gene might be associated with the susceptibility of MDD patients through affecting the bioeffects of endogenous dopamine neurotransmission. However, little is known about their occurrence in Chinese population and their association with the susceptibility of patients with major depressive disorder. In this study, a total of 338 unrelated adult Chinese Han population, including 224 healthy volunteers and 114 patients with major depressive disorder, were recruited. DRD2 polymorphisms (Taq1A and -141C ins/del) were detected using restriction fragment length polymorphism (RFLP) analysis and the C957T were detected by sequencing directly. As a result, three polymorphisms were identified in Chinese Han population and all were common SNP. However, we could detect no evidence of genetic association between 3 markers in DRD2 and major depressive disorder in the Chinese Han population. To conclude, this result suggests that Taq1A, C957T and -141C ins/del of DRD2 gene may not be associated with major depressive disorder, also may be the sample sizes too small to allow a meaningful test.


Subject(s)
Asian People/genetics , Depressive Disorder, Major/genetics , Polymorphism, Single Nucleotide , Receptors, Dopamine D2/genetics , Adolescent , Adult , Analysis of Variance , Case-Control Studies , Chi-Square Distribution , China/epidemiology , Depressive Disorder, Major/diagnosis , Depressive Disorder, Major/ethnology , Female , Gene Frequency , Genetic Association Studies , Genetic Predisposition to Disease , Humans , Linear Models , Logistic Models , Male , Middle Aged , Phenotype , Risk Factors , Young Adult
8.
Int J Med Sci ; 9(8): 655-64, 2012.
Article in English | MEDLINE | ID: mdl-23055817

ABSTRACT

This study was conducted to characterize the intracranial pressure response to non-penetrating ballistic impact using a "scalp-skull-brain" pig physical head model and live pigs. Forty-eight ballistic tests targeting the physical head model and anesthetized pigs protected by aramid plates were conducted with standard 9 mm bullets at low (279-297 m/s), moderate (350-372 m/s), and high (409-436 m/s) velocities. Intracranial pressure responses were recorded with pressure sensors embedded in similar brain locations in the physical head model and the anesthetized pigs. Three parameters of intracranial pressure were determined from the measured data: intracranial maximum pressure (P(max)), intracranial maximum pressure impulse (PI(max)), and the duration of the first positive phase (PPD). The intracranial pressure waves exhibited blast-like characteristics for both the physical model and l live pigs. Of all three parameters, P(max) is most sensitive to impact velocity, with means of 126 kPa (219 kPa), 178 kPa (474 kPa), and 241 kPa (751 kPa) for the physical model (live pigs) for low, moderate, and high impact velocities, respectively. The mean PPD becomes increasingly short as the impact velocity increases, whereas PI(max) shows the opposite trend. Although the pressure parameters of the physical model were much lower than those of the live pigs, good correlations between the physical model and the live pigs for the three pressure parameters, especially P(max), were found using linear regression. This investigation suggests that P(max) is a preferred parameter for predicting the severity of the brain injury resulting from behind armor blunt trauma (BABT).


Subject(s)
Forensic Ballistics , Head , Models, Anatomic , Analysis of Variance , Animals , Intracranial Pressure , Swine
9.
J Neurol Sci ; 294(1-2): 23-8, 2010 Jul 15.
Article in English | MEDLINE | ID: mdl-20478573

ABSTRACT

Blast-induced traumatic brain injury (TBI) has been the predominant cause of neurotrauma in current military conflicts, and it is also emerging as a potential threat in civilian terrorism. The etiology of TBI, however, is poorly understood. Further study on the mechanisms and treatment of blast injury is urgently needed. We developed a unique rat model to simulate blast effects that commonly occur on the battlefield. An electric detonator with the equivalent of 400 mg TNT was developed as the explosive source. The detonator's peak overpressure and impulse of explosion shock determined the explosion intensity in a distance-dependent manner. Ninety-six male adult Sprague-Dawley rats were randomly divided into four groups: 5-cm, 7.5-cm, 10-cm, and control groups. The rat was fixed in a specially designed cabin with an adjustable aperture showing the frontal, parietal, and occipital parts of the head exposed to explosion; the eyes, ears, mouth, and nose were protected by the cabin. After each explosion, we assessed the physiologic, neuropathologic, and neurobehavioral consequences of blast injury. Changes of brain tissue water content and neuron-specific enolase (NSE) expression were detected. The results in the 7.5-cm group show that 87% rats developed apnea, limb seizure, poor appetite, and limpness. Diffuse subarachnoid hemorrhage and edema could be seen within the brain parenchyma, which showed a loss of integrity. Capillary damage and enlarged intercellular and vascular space in the cortex, along with a tattered nerve fiber were observed. These findings demonstrate that we have provided a reliable and reproducible blast-induced TBI model in rats.


Subject(s)
Blast Injuries/complications , Brain Injuries/etiology , Disease Models, Animal , Animals , Apnea/etiology , Apnea/pathology , Apnea/physiopathology , Blast Injuries/pathology , Blast Injuries/physiopathology , Brain/pathology , Brain/physiopathology , Brain Edema/etiology , Brain Edema/pathology , Brain Edema/physiopathology , Brain Injuries/pathology , Brain Injuries/physiopathology , Electronics , Equipment Design , Immunohistochemistry , Male , Phosphopyruvate Hydratase/blood , Phosphopyruvate Hydratase/metabolism , Pressure , Random Allocation , Rats , Rats, Sprague-Dawley , Seizures/etiology , Seizures/pathology , Seizures/physiopathology , Time Factors
10.
Zhongguo Zhong Xi Yi Jie He Za Zhi ; 29(12): 1100-3, 2009 Dec.
Article in Chinese | MEDLINE | ID: mdl-20214332

ABSTRACT

OBJECTIVE: To seek an effective drug for treatment of human hyperplastic scar through studying the effects of curcumin on fibroblast growth and collagen synthesis. METHODS: Fibroblasts derived from scar tissue and from normal epidermal tissue were isolated and cultured separately with tissue-block method, their morphology were observed under invert phase contrast microscope, their growth curve was drawn respectively to determine the speed of growth. Then, fibroblasts from scar were stimulated with curcumin in different concentrations (0, 12.5, 25, 50 and 100 micromol/L) for detecting the inhibitory effect of curcumin on growth of fibroblasts using MTT methods and that on activity of procollagen alpha-1 gene transcription in fibroblast was detected by RT-PCR. RESULTS: The cell growth curve showed that double-multiplying time was 5 days in fibroblasts from scar and 4 days in those from normal dermis, showing significant difference between them (P < 0.05). MTT showed that curcumin in 12.5 micromol/L showed a cell proliferation enhancing trend, and its absorbance value was significantly higher than that in the normal group, but the effect turned to inhibition when concentration increased to over 25-100 micromol/L, and became significant inhibition at concentration of 50 and 100 micromol/L. Besides, curcumin also showed markedly inhibition on collagen type I synthesis in fibroblasts (P < 0.01). CONCLUSION: High concentration curcumin can inhibit effectively the fibroblast proliferation and collagen I synthesis in hyperplastic scar, therefore, may has therapeutic effect on the disease in human being.


Subject(s)
Cicatrix, Hypertrophic/metabolism , Cicatrix, Hypertrophic/pathology , Curcumin/pharmacology , Fibroblasts/drug effects , Cell Proliferation/drug effects , Cells, Cultured , Collagen Type I/biosynthesis , Fibroblasts/metabolism , Fibroblasts/pathology , Humans
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