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1.
Int J Cancer ; 47(6): 843-6, 1991 Apr 01.
Article in English | MEDLINE | ID: mdl-2010226

ABSTRACT

A total of 55 formalin-fixed and paraffin-embedded specimens of normal, inflamed and neoplastic uterine cervix have been studied in order to correlate the epithelial changes with the expression of alpha-smooth-muscle actin in stromal cells. This actin isoform is typical of smooth-muscle cells, but appears also temporarily in fibroblasts during wound healing and permanently during fibrocontractive diseases and stromal reaction to epithelial tumors. While positive stromal cells were absent in normal and inflamed cervix, they accumulated in relation to neoplastic tissues. The number of alpha-smooth-muscle actin positive cells and the intensity of stain were related to the increasing grading of cervical intra-epithelial neoplasia. Our results suggest that alpha-smooth-muscle actin is a marker of stromal-cell reaction to the development of neoplastic lesions. The evaluation of alpha-smooth-muscle actin in stromal cells of the uterine cervix may be a useful adjunct to diagnostic criteria of cervical intra-epithelial neoplasia and may help understanding of the mechanisms of mesenchymal-epithelial interactions during neoplasia.


Subject(s)
Actins/analysis , Carcinoma, Squamous Cell/pathology , Cervix Uteri/pathology , Uterine Cervical Dysplasia/pathology , Uterine Cervical Neoplasms/pathology , Epithelium/pathology , Female , Humans , Immunoenzyme Techniques , Muscle, Smooth/pathology , Neoplasm Invasiveness
2.
Pathol Res Pract ; 185(6): 848-55, 1989 Dec.
Article in English | MEDLINE | ID: mdl-2482482

ABSTRACT

In this study antibodies specific for different intermediate-sized proteins (cytokeratins and neurofilaments) have been tested on a series of neuroendocrine (NE) lung tumors in order to evaluate their diagnostic validity. In particular we used a panel of polyclonal anti-neurofilament 200-kilodalton subunits whose reactivity against phospho-dependent epitopes was known. At least one NF subunit was constantly present and in all cases coexpression of cytokeratins and neurofilaments was confirmed. However, in cases of carcinoid tumor (CT) the results were homogeneous, while the cases of small cell lung carcinoma (SCLC) showed a much wider range of immunostaining. Our investigation confirms the hypothesis that the phosphorylation state is a significant determinant of immunohistochemical properties of neurofilaments. This might explain the large number of negative results obtained in previous investigations on NE tumors. The phosphorylation of neurofilaments may also be considered an indication of the degree of differentiation of the tumor.


Subject(s)
Carcinoma, Small Cell/metabolism , Carcinoma/metabolism , Intermediate Filament Proteins/metabolism , Keratins/metabolism , Lung Neoplasms/metabolism , Biomarkers, Tumor/analysis , Carcinoma/analysis , Carcinoma/pathology , Carcinoma, Small Cell/analysis , Carcinoma, Small Cell/pathology , Humans , Immunohistochemistry , Intermediate Filament Proteins/analysis , Keratins/analysis , Lung Neoplasms/analysis , Lung Neoplasms/pathology , Phosphorylation
4.
Arch Gynecol Obstet ; 241(4): 235-47, 1988.
Article in English | MEDLINE | ID: mdl-2835017

ABSTRACT

A series of 64 punch biopsies collected from women prospectively followed-up for cervical Human papillomavirus (HPV) infections (with and without CIN), and 38 control biopsies (normal epithelia, and classical CIN) were analysed for expression of filaggrin (a histidine-rich protein constituent of keratohyalin granules) using the ABC technique and polyclonal antibody. HPV typing was completed using the in situ hybridization technique with DNA probes for HPV 6, 11, 16, 18 and 31. Three patterns of filaggrin distribution were differentiated: pattern I, all layers above the basal cells stained positive regularly; pattern II, all layers above the basal cells stained irregularly, and pattern III, scattered superficial cells stained positive. There was a significant difference between HPV-noCIN and HPV-CIN lesions in their filaggrin patterns, pattern I being present in the majority (77.7%) of HPV-noCIN lesions, as contrasted to HPV-CIN lesions, where pattern III was the predominant one (43.5%), followed by pattern II (32.6%). In HPV-CIN as well as in CIN lesions, pattern I was inversely related to the grade of CIN, being entirely absent in HPV-CIN III and CIN III. A significant difference exists between CIN and HPV-CIN lesions, concerning the presence of pattern III (4.3% and 43.5%, respectively, P less than 0.001). The difference was less dramatic with regard to pattern I (30.4% and 21.7%, respectively, P less than 0.05). In the lesions containing HPV 6, 11 or 31 DNA, filaggrin distribution was shown to be more close to that of the normal epithelium (I 36.7%, and II 34.7%), while in the HPV 16 and 18-infected cases, pattern III was the predominant one (46.7%). The assessment of filaggrin pattern in HPV lesions might be of help in evaluating the severity of the disturbance of keratinocyte differentiation induced by the progression of HPV infections.


Subject(s)
Cervix Uteri/analysis , Intermediate Filament Proteins/analysis , Tumor Virus Infections/metabolism , Uterine Cervical Neoplasms/analysis , DNA, Viral/analysis , Female , Filaggrin Proteins , Humans , Immunoenzyme Techniques , Papillomaviridae/classification , Uterine Cervical Neoplasms/microbiology
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