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1.
Protein Pept Lett ; 31(1): 25-42, 2024.
Article in English | MEDLINE | ID: mdl-38155464

ABSTRACT

Protein arginine methylation stands as a prevalent post-translational modification process, exerting vital roles in cellular signal transduction, gene expression, and cell cycle regulation. Amidst the protein arginine methyltransferase (PRMT) family, PRMT2 stands as a less explored constituent. Nonetheless, its regulatory roles in transcriptional regulation, post-transcriptional modification, methylation activity regulation, immunoregulation, and developmental regulation have garnered attention. These capabilities enable PRMT2 to exert pivotal regulatory functions in certain malignancies, metabolic disorders, inflammatory diseases, and atherosclerosis. In this review, we highlight the structure and functions of PRMT2, emphasizing its association with diseases. We also discuss PRMT2 inhibitors and explore the potential for therapeutic targeting.


Subject(s)
Gene Expression Regulation , Protein-Arginine N-Methyltransferases , Protein-Arginine N-Methyltransferases/genetics , Methylation , Protein Processing, Post-Translational , Arginine
2.
BMJ ; 381: e071601, 2023 05 11.
Article in English | MEDLINE | ID: mdl-37169374

Subject(s)
Penis , Ulcer , Male , Humans , Pain/etiology , Pelvis
3.
Brain Res ; 1718: 64-74, 2019 09 01.
Article in English | MEDLINE | ID: mdl-31075261

ABSTRACT

Emerging evidence implicates the upregulation of matrix metalloproteinase (MMP)-9/2 in the dorsal root ganglion (DRG) and spinal cord as a contributor to the pathogenesis of chronic pain. In the current study, the expression of MMP-9/2 in wounded tissue, ipsilateral DRG, and the spinal dorsal horn as well as its role in the development of postoperative pain were examined following plantar incision in rats. Our results showed that plantar incision resulted in increased expression of MMP-9/2 in wounded tissue and ipsilateral L4/5 DRGs. Although gelatin zymography detected an increased activity of MMP-9, only MMP-2 protein was increased in the spinal cord. Results of double immunofluorescence staining showed MMP-2 expression in DRG neurons and satellite glial cells, but MMP-9 was found only in neurons. In the spinal cord, MMP-2 was expressed in neurons and astrocytes, and MMP-9 was expressed in neurons and somewhat in microglial cells. Planter incision also elicited increased expression of p-Erk, p-p38, and IL-1ß in wounded tissue, ipsilateral L4/5 DRGs, and dorsal horn. Prior intraplantar or intrathecal injection of MMP-9- and MMP-2-specific inhibitors partially prevented reductions of paw withdrawal threshold and paw withdrawal latency following plantar incision. The maturation of IL-1ß was also inhibited by the treatment. Moreover, MMP-9 inhibition suppressed p38, and MMP-2 inhibitor reduced the Erk phosphorylation in wounded tissue, DRGs, and dorsal horn. Immunofluorescence staining detected colocalization of MMP-9 with p38 and MMP-2 with Erk in DRG and spinal cord. Together, the above results reveal that upregulated MMP-9 via p38/IL-1ß and MMP-2 via Erk/IL-1ß signaling in the wounded tissue, ipsilateral DRG, and dorsal horn contribute to the development of postoperative pain.


Subject(s)
Ganglia, Spinal/metabolism , Matrix Metalloproteinase 2/metabolism , Matrix Metalloproteinase 9/metabolism , Pain, Postoperative/metabolism , Spinal Cord/metabolism , Wound Healing/physiology , Animals , Hyperalgesia/metabolism , Interleukin-1beta , MAP Kinase Signaling System , Male , Microglia/metabolism , Neuroglia/metabolism , Pain Measurement , Rats , Rats, Sprague-Dawley , Signal Transduction , Spinal Cord Dorsal Horn/metabolism , p38 Mitogen-Activated Protein Kinases/metabolism
4.
Melanoma Res ; 27(3): 175-179, 2017 06.
Article in English | MEDLINE | ID: mdl-28225433

ABSTRACT

Malignant melanoma is a highly aggressive neoplasia of melanocytic origin. In part because of the lack of effective treatment methods, the incidence and mortality rates of this disease continue to increase. Rapidly accumulating evidence suggests that dysregulation of epigenetic mechanisms, including DNA methylation/demethylation, chromatin modification, and remodeling, and diverse activities of noncoding RNAs, play a central role in the pathogenesis of melanoma. The epigenetic mark 5-hydroxymethylcytosine (5-hmC) has attracted interest since 2009, when it was shown that ten-eleven translocation proteins can enzymatically convert 5-methylcytosine into 5-hmC, a key intermediate of DNA demethylation. Factors that regulate DNA hydroxymethylation are frequently altered in cancer, leading to deregulation of 5-hmC levels. In this review, we will discuss the relationship between melanoma and DNA hydroxymethylation, the regulation of DNA hydroxymethylation, and defects in this pathway in melanoma.


Subject(s)
5-Methylcytosine/analogs & derivatives , DNA Methylation , Epigenesis, Genetic , Melanoma/genetics , 5-Methylcytosine/chemistry , Humans
5.
Acta Crystallogr Sect E Struct Rep Online ; 68(Pt 5): o1515, 2012 May 01.
Article in English | MEDLINE | ID: mdl-22590382

ABSTRACT

In the title compound, C(20)H(11)Cl(2)F(4)N(3), the central pyrazolo-[1,5-a]pyrimidine unit is almost planar [the mean deviation from the best least-square plane through the nine atoms is 0.006 (2) Å]. The fluoro-benzene ring is rotated out of this plane by 10.3 (3)°, whereas the dichloro-benzene ring is rotated by 46.2 (3)°. The crystal packing is dominated by Cl⋯Cl inter-actions of 3.475 (3) Šand van der Waals inter-actions.

6.
J Plast Reconstr Aesthet Surg ; 61(3): 338-41, 2008.
Article in English | MEDLINE | ID: mdl-18267314

ABSTRACT

Epidermodysplasia Verruciformis is a rare skin disease due to human papillomavirus (HPV) infection. We report here a male patient of 39 years with severe giant lesion of hands and feet leading to disability for 20 years. The function of the hands was almost lost. We treated the case with the shaving technique and a satisfactory result without recrudescence in the following two years. No apparent scarring resulted.


Subject(s)
Epidermodysplasia Verruciformis/surgery , Foot Deformities, Acquired/surgery , Hand Deformities, Acquired/surgery , Adult , Epidermodysplasia Verruciformis/complications , Epidermodysplasia Verruciformis/pathology , Foot Deformities, Acquired/pathology , Foot Deformities, Acquired/virology , Hand Deformities, Acquired/pathology , Hand Deformities, Acquired/virology , Hand Dermatoses/pathology , Hand Dermatoses/surgery , Hand Dermatoses/virology , Humans , Male , Plastic Surgery Procedures/methods
7.
Fa Yi Xue Za Zhi ; 22(1): 58-60, 69, 2006 Feb.
Article in Chinese | MEDLINE | ID: mdl-16524190

ABSTRACT

OBJECTIVE: To explore the criminological characteristics of mental retardation (MR) in forensic psychiatry. METHODS: The record scale of forensic psychiatric assessment designed by ourselves was used to analyse the criminological characteristics of 83 offenders with MR, and to compare the criminological characteristics of mild MR with that of moderate and severe MR. RESULTS: The mild MR accounted for 62.7%, moderate and severe MR was 22.9%. The percentage of sex offenders in MR was 37.3%, manslaughter 34.7%, property offences 28.0%, respectively. Additionally, 96.1% cases with MR have definite criminal motives, and the criminal history was established in 34.7% cases. Significant differences of criminal premeditation (X2chi-squared l11,P=0.001), criminal aim(x2chi-squared 7.531, P=0.006), criminal motive(X 2chi-squared . 920, P= 0.019) and criminal types(s 2chi-squared .855, P=0.02) were found between the mild MR and the moderate, severe MR. CONCLUSIONS: The criminal offenders were mostly found in mild MR. The sex offenders and manslaughter were in outright majority, and most of them had definite criminal motives. The proportion of offenders in mild MR who had criminal premeditation and criminal aim was higher significantly than which in the moderate, severe MR. The proportion of offenders in moderate, severe MR whose criminal motive was for sex was higher than that in mild MR.


Subject(s)
Crime/psychology , Forensic Psychiatry/methods , Intellectual Disability/psychology , Adolescent , Adult , Crime/statistics & numerical data , Expert Testimony , Female , Forensic Psychiatry/statistics & numerical data , Homicide/psychology , Homicide/statistics & numerical data , Humans , Male , Middle Aged , Risk Factors , Severity of Illness Index , Sex Offenses/psychology , Sex Offenses/statistics & numerical data , Young Adult
8.
Chin Med Sci J ; 20(4): 273-5, 2005 Dec.
Article in English | MEDLINE | ID: mdl-16422259

ABSTRACT

OBJECTIVE: To establish a multiplex polymerase chain reaction (M-PCR) assay for simultaneous detection of pathogens causing genital ulcer disease (GUD). METHODS: Based on the gene-specific region of the following pathogens: Chlamydia trachomatis omp1/ompb, herpes simplex virus (HSV) DNA polymerase, Treponema pallidum tpp47, Haemophilus ducreyi 16s rRNA, four sets of primers were designed and an M-PCR assay was developed to detect four pathogens in one test. The assay was evaluated with diagnostic result of golden standard for each pathogen. RESULTS: Of the 51 clinical samples, M-PCR showed slightly higher positive rate (47.1%) of HSV than cell culture (23.6%). Meanwhile, the positive rate of T. pallidum detected by M-PCR and dark-field microscopy was 19.6% (10/51) and 15.7% (8/51), respectively. Only one sample was positive for H. ducreyi and no sample was positive for C. trachomatis detected by both M-PCR assay and culture. CONCLUSION: This primary study indicated that M-PCR assay can simultaneously and rapidly detect the four etiologic pathogens causing GUD.


Subject(s)
Herpesvirus 1, Human/isolation & purification , Herpesvirus 2, Human/isolation & purification , Sexually Transmitted Diseases/virology , Treponema pallidum/isolation & purification , Ulcer/virology , Chlamydia trachomatis/genetics , Chlamydia trachomatis/isolation & purification , DNA Primers , Haemophilus ducreyi/genetics , Haemophilus ducreyi/isolation & purification , Herpesvirus 1, Human/genetics , Herpesvirus 2, Human/genetics , Humans , Polymerase Chain Reaction/methods , Sexually Transmitted Diseases/complications , Sexually Transmitted Diseases/microbiology , Treponema pallidum/genetics , Ulcer/complications , Ulcer/microbiology
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