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1.
Eur J Surg Oncol ; 28(2): 103-7, 2002 Mar.
Article in English | MEDLINE | ID: mdl-11884043

ABSTRACT

AIMS: p21, an inhibitor of cyclin-dependent kinase, is involved in the p53 pathway of growth control. Its expression has been linked to cellular differentiation. It has been implicated in p53-mediated growth arrest following DNA damage and in terminally differentiated cells. This study analysed p21 and p53 expression, in a series of node-positive patients with breast carcinoma and examined histopathological parameters of the tumour and the prognostic implications of p21 and p53 expression. METHODS: One hundred and five consecutive patients with node-positive disease and at least 3 years follow-up were identified. Sections were stained for p53 and p21 using monoclonal antibodies. Results were expressed as percentage positive cells, and over 20% considered positive for p53 and over 10% considered for p21. RESULTS: p21 was overexpressed (>10% of cells positive) in 65% of patients and p53 was overexpressed (>20% of cells positive in 68%. The mean (SEM) level of p21 staining was 5.7(0.8)% and was 54.9(4.0)% for p53. There was no correlation between p21 and p53 expression (r=0.071 P=0.5). There were no significant differences in demographic criteria between patients that were p21 positive or negative and p53 positive or negative. There were no significant differences in tumour type, grade or stage between the groups. p21 expression did not have prognostic significance; however, p53 positivity was associated with a worse prognosis, which remained when controlled for stage. CONCLUSIONS: This study demonstrated p21 overexpression in 65% of patients with node-positive breast carcinoma. Levels did not correlate with p53 status and unlike p53 failed to have prognostic significance.


Subject(s)
Adenocarcinoma/pathology , Adenocarcinoma/secondary , Biomarkers, Tumor/analysis , Breast Neoplasms/pathology , Cyclins/analysis , Lymph Nodes/pathology , Tumor Suppressor Protein p53/analysis , Aged , Cohort Studies , Cyclin-Dependent Kinase Inhibitor p21 , Female , Follow-Up Studies , Humans , Immunohistochemistry , Lymphatic Metastasis , Middle Aged , Neoplasm Staging , Probability , Prognosis , Prospective Studies , Sensitivity and Specificity
2.
Int J Cancer ; 91(5): 692-7, 2001 Mar 01.
Article in English | MEDLINE | ID: mdl-11267982

ABSTRACT

Patients suffering from nasopharyngeal carcinoma (NPC) generally exhibit elevated serum IgA antibody titres to Epstein-Barr virus (EBV) early antigen (EA) and virus capsid antigen (VCA). This property is frequently used as a diagnostic aid. Preliminary experiments suggested that an ELISA for IgA antibodies against the EBV-encoded thymidine kinase (TK) could form the basis of a more reliable diagnostic test. Here, we describe the construction of a recombinant baculovirus that expresses the EBV TK and present a full analysis of its use in serological surveys of NPC patients. Baculovirus-derived TK was used to develop a simple ELISA for serum IgA against this antigen. ELISA reactivity was strongly associated with NPC compared with an EBV-positive, normal control population. Comparison with the existing IgA-VCA and EA assays showed that the TK ELISA had higher sensitivity whilst the specificity was similar or higher. We conclude that the TK ELISA presents a strong predictor of NPC and, in its refined form, has improved pickup rates. In addition, results from patients with chronic nasopharyngitis (CNP) suggest that individuals with both symptoms of CNP and an elevated TK ELISA value may be at increased risk for the development of head-and-neck cancer.


Subject(s)
Antibodies , Biomarkers, Tumor , Carcinoma/blood , Herpesvirus 4, Human/enzymology , Nasopharyngeal Neoplasms/blood , Thymidine Kinase/immunology , Animals , Baculoviridae/enzymology , Carcinoma/diagnosis , Carcinoma/enzymology , Carcinoma/virology , Cell Line , Enzyme-Linked Immunosorbent Assay , Humans , Immunoglobulin A/blood , Insecta , Microscopy, Fluorescence , Nasopharyngeal Neoplasms/diagnosis , Nasopharyngeal Neoplasms/enzymology , Nasopharyngeal Neoplasms/virology , Nasopharyngitis/blood , Nasopharyngitis/enzymology , Pilot Projects , Risk Factors , Thymidine Kinase/blood , Time Factors
3.
Death Stud ; 24(4): 275-305, 2000 Jun.
Article in English | MEDLINE | ID: mdl-11010730

ABSTRACT

A longitudinal study of 144 parents (65 fathers, 79 mothers) was conducted to evaluate the effectiveness of a program of intervention in relieving the psychological distress of parents affected by infant death. Participants were assessed in terms of their psychiatric disturbance, depression, anxiety, physical symptoms, dyadic adjustment, and coping strategies. The experimental group (n = 84) was offered an intervention program comprising the use of specially designed resources and contact with a trained grief worker. A control group (n = 60) was given routine community care. Parental reactions were assessed at four to six weeks postloss (prior to the implementation of the intervention program), at six months postloss, and at 15 months postloss. A series of multivariate analyses of variance revealed that the intervention was effective in reducing the distress of parents, particularly those assessed prior to the intervention as being at high-risk of developing mourning difficulties. Effects of the intervention were noted in terms of parents' overall psychiatric disturbance, marital quality, and paternal coping strategies.


Subject(s)
Bereavement , Death , Infant , Parents/psychology , Program Evaluation , Adaptation, Psychological , Adolescent , Adult , Australia , Female , Humans , Longitudinal Studies , Male , Middle Aged , Multivariate Analysis , Psychological Tests , Risk Factors
4.
Neuroreport ; 10(10): 2209-13, 1999 Jul 13.
Article in English | MEDLINE | ID: mdl-10424700

ABSTRACT

N- and C-terminal substance P (SP) fragments increase striatal dopamine outflow at nanomolar concentrations. This contrasts with their low affinity for NK1 receptors. To explore this discrepancy, we investigated the interaction of SP and SP fragments with NK1 sites in fresh striatal slices, the same model used in the functional studies on dopamine outflow. [3H]SP bound specifically to one site (Kd = 6.6 +/- 0.9 nM; Bmax = 12.6 +/- 0.7 fmol/mg protein). [3H]SP binding was displaced by SP (IC50 = 11.8 nM), but not by SP(1-7) or SP(5-11), up to 10 microM. In contrast, 10 nM SP(1-7) or SP(5-11) induced significant internalization of the NK1 receptor, similar to that induced by SP. We suggest that SP fragments have high affinity for an NK1 receptor conformer which is different from that labelled by [3H]SP.


Subject(s)
Corpus Striatum/metabolism , Peptide Fragments/metabolism , Receptors, Neurokinin-1/metabolism , Substance P/metabolism , Analysis of Variance , Animals , In Vitro Techniques , Male , Rats , Rats, Wistar , Substance P/chemistry
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