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1.
Toxicol Appl Pharmacol ; 255(1): 65-75, 2011 Aug 15.
Article in English | MEDLINE | ID: mdl-21683088

ABSTRACT

Exposure during early development to chemicals with hormonal action may be associated with weight gain during adulthood because of altered body homeostasis. It is known that organotins affect adipose mass when exposure occurs during fetal development, although no knowledge of effects are available for exposures after birth. Here we show that the environmental organotin tributyltin chloride (TBT) exerts adipogenic action when peripubertal and sexually mature mice are exposed to the chemical. The duration and extent of these effects depend on the sex and on the dose of the compound, and the effects are relevant at doses close to the estimated human intake (0.5µg/kg). At higher doses (50-500µg/kg), TBT also activated estrogen receptors (ERs) in adipose cells in vitro and in vivo, based on results from acute and longitudinal studies in ERE/luciferase reporter mice. In 3T3-L1 cells (which have no ERs), transiently transfected with the ERE-dependent reporter plus or minus ERα or ERß, TBT (in a dose range of 1-100nM) directly targets each ER subtype in a receptor-specific manner through a direct mechanism mediated by ERα in undifferentiated preadipocytic cells and by ERß in differentiating adipocytes. The ER antagonist ICI-182,780 inhibits this effect. In summary, the results of this work suggest that TBT is adipogenic at all ages and in both sexes and that it might be an ER activator in fat cells. These findings might help to resolve the apparent paradox of an adipogenic chemical being also an estrogen receptor activator by showing that the two apparently opposite actions are separated by the different doses to which the organism is exposed.


Subject(s)
Adipose Tissue/drug effects , Environmental Pollutants/toxicity , Receptors, Estrogen/drug effects , Trialkyltin Compounds/toxicity , 3T3-L1 Cells , Adipocytes/drug effects , Animals , Diethylstilbestrol/pharmacology , Dose-Response Relationship, Drug , Estradiol/pharmacology , Female , Male , Mice , Mice, Inbred C57BL , PPAR gamma/physiology
2.
Int J Gynecol Cancer ; 18(1): 14-21, 2008.
Article in English | MEDLINE | ID: mdl-17451461

ABSTRACT

Uterine serous papillary carcinoma (USPC) is a rare and highly malignant form of endometrial cancer (EC) characterized by early metastasis, chemoresistance, and high mortality rate. Little is known about USPC tumorigenesis even if recently a HER-2/neu role has been suggested in its development and progression. The aim of the present study was to evaluate HER-2 expression by immunohistochemistry (IHC) in 12 USPC formalin-fixed, paraffin-embedded (FFPE) samples. Moreover, we looked at the correlation between HER-2 protein expression and HER-2/neu gene amplification by fluorescence in situ hybridization (FISH), other than HER-2/neu messenger RNA expression by quantitative real-time reverse transcription (RT)-polymerase chain reaction (PCR). Finally, these results have been compared with commonly evaluated clinical features in EC patients, in order to define the potential prognostic value of HER-2/neu overexpression in USPCs. A high expression of HER-2 protein by IHC was noted in 2 of 12 patients (16.6%), and the same cases showed specific HER-2/neu gene amplification by FISH. All the samples investigated displayed a perfect concordance between IHC and FISH data. Five (41.6%) of 12 tumors demonstrated polysomy of chromosome 17 and, focusing on the 2 USPCs that showed HER-2/neu overexpression, one of them (50%) was polysomic for chromosome 17. All the other USPC cases (58.4%) showed to be disomic for chromosome 17. Quantitative RT real-time PCR performed on complementary DNA obtained from all FFPE USPC samples showed a complete correlation with FISH and IHC data. Moreover, HER-2/neu overexpression was associated with a poorer overall survival and a very low relapse-free survival time, thus being considered a candidate marker of worse overall prognosis in USPC. The use of trastuzumab (Herceptin), a monoclonal antibody directed against HER-2/neu, for the therapy of patients with HER-2/neu-positive USPCs should be further investigated in clinical trials.


Subject(s)
Cystadenocarcinoma, Papillary/genetics , Gene Amplification , Receptor, ErbB-2/genetics , Receptor, ErbB-2/metabolism , Uterine Neoplasms/genetics , Uterine Neoplasms/metabolism , Aged , Aged, 80 and over , Cystadenocarcinoma, Papillary/metabolism , Cystadenocarcinoma, Papillary/pathology , Female , Humans , Immunoenzyme Techniques , In Situ Hybridization, Fluorescence , Lymph Nodes/pathology , Middle Aged , Neoplasm Invasiveness/pathology , Paraffin Embedding , Prognosis , Reverse Transcriptase Polymerase Chain Reaction , Survival Rate , Uterine Neoplasms/pathology
3.
Endocrinology ; 147(12): 5740-51, 2006 Dec.
Article in English | MEDLINE | ID: mdl-16959845

ABSTRACT

The soy isoflavone genistein targets adipose tissue and elicits physiological effects that may vary based on dietary intake. We hypothesized that the adipose effects of genistein are dose and gender dependent. Four-week-old C57BL/6 male and female mice received daily oral doses of genistein (50-200,000 microg/kg.d) or 17beta-estradiol (E2) (5 microg/kg.d) for 15 d or a diet containing 800 ppm genistein. Genistein increased epididymal and renal fat pad and adipocyte size at doses up to 50,000 microg/kg.d or at 800 ppm in the diet in males but not in females. The alteration in adipocity correlated with changes in peripheral insulin resistance. These treatments increased genistein serum concentrations from 35+/-6 to 103+/-26 nM 12 h after treatment and lowered plasma triglycerides and cholesterol levels. The 200,000 microg/kg.d genistein dose decreased adipose tissue weight similarly to E2. This genistein dose down-regulated estrogen receptor (beta more than alpha) and progesterone receptor expression and induced estrogen-dependent adipose differentiation factors; it did not change expression of the minimal consensus estrogen-responsive element in ERE-tK-LUC mice, which was positively modulated in other tissues (e.g. the lung). E2 down-regulated almost all examined adipogenic factors. Gene microarray analysis identified factors in fat metabolism and obesity-related phenotypes differentially regulated by low and high doses of genistein, uncovering its adipogenic and antiadipogenic actions. The lower dose induced the phospholipase A2 group 7 and the phospholipid transfer protein genes; the 200,000 microg/kg.d dose inhibited them. The antiadipogenic action of genistein and down-regulation of adipogenic genes required the expression of ERbeta. In conclusion, nutritional doses of genistein are adipogenic in a gender-specific manner, whereas pharmacological doses inhibited adipose deposition.


Subject(s)
Adipose Tissue/drug effects , Body Composition/drug effects , Genistein/pharmacology , Sex Characteristics , Adipocytes/cytology , Animals , Body Fat Distribution , Cell Count , Cell Differentiation/drug effects , Cell Differentiation/genetics , Cell Size/drug effects , Dose-Response Relationship, Drug , Drug Administration Schedule , Epididymis , Estrogen Receptor beta/physiology , Female , Gene Expression Profiling , Genistein/administration & dosage , Kidney , Lipogenesis/drug effects , Lipogenesis/genetics , Male , Mice , Mice, Inbred C57BL , Mice, Knockout , Mice, Transgenic , Receptors, Estrogen/genetics , Receptors, Estrogen/metabolism
4.
Eur J Histochem ; 48(3): 329-34, 2004.
Article in English | MEDLINE | ID: mdl-15590423

ABSTRACT

Qualitative evaluation of protein content in formalin fixed, paraffin-embedded tissues is usually performed by means of cytofluorimetric analysis. On the other hand, several studies underline the opportunity to measure the concentration of nuclear proteins, which is often accomplished by using complex techniques and instrumentation. In the present work, we suggest a new application for the spectrophotometric evaluation of protein content on extracted and isolated nuclei, based on EDTA treatment of specimens and chemical extraction of proteins, followed by direct spectrophotometric measurement at UV wavelengths. We also demonstrate how this parameter correlates with other diagnostic factors, such as the proliferation index (MIB-1) and the DNA content (ploidy) of cells. This method is simple and effective, yet less expensive than other protein quantitation protocols.


Subject(s)
Breast Neoplasms/chemistry , Nuclear Proteins/analysis , Spectrophotometry/methods , Breast Neoplasms/pathology , Cell Nucleus/chemistry , Cell Nucleus/pathology , DNA, Neoplasm/analysis , DNA, Neoplasm/isolation & purification , Female , Fixatives/chemistry , Flow Cytometry , Formaldehyde/chemistry , Humans , Immunohistochemistry , Ki-67 Antigen/analysis , Nuclear Proteins/chemistry , Nuclear Proteins/isolation & purification , Paraffin Embedding , Ploidies , Tissue Fixation
6.
Eur Urol ; 43(6): 680-5, 2003 Jun.
Article in English | MEDLINE | ID: mdl-12767370

ABSTRACT

OBJECTIVES: The Heidelberg classification of renal tumours identifies five histotypes of renal cancer, underlining for two of them (conventional and papillary renal cancers) a strict relation between the morphological aspect and the complement of alterations evidenced by the cytogenetic analysis of the neoplastic karyotype. Due to its low incidence, the collecting duct carcinoma (CDC) has not yet been characterized from a cytogenetic point of view. This study analyses the clinical, morphologic and cytogenetic features of the CDC observed and treated in our department. METHODS: From January 1995 to December 2002, among the 591 patients who underwent surgery for renal cancer, we observed 11 cases of CDC (prevalence 1.9%) treated either by radical (9 cases) or partial nephrectomy (2 cases). During radical nephrectomy a loco-regional lymphadenectomy was always performed. In the 9 cases observed after 1997, a complete cytogenetic analysis of the neoplastic karyotype was carried out. RESULTS: At pathological examination the disease was found to be confined to the renal capsule (TNM 1997 stage 1) in only 3 patients; venous neoplastic trombosis and nodal metastasis were present in 3 and 6 cases respectively; 2 patients showed distant metastases (lung, bone). Two of the patients affected with stage 1 tumours are still alive with no evidence of the disease at 48 and 88 months after surgery, while the third died following the systemic progression of a concomitant bladder carcinoma. One patient with stage 4 tumour (no. 11) is alive, but the follow up time is still limited (2 months). All the other 7 patients are dead after a mean survival time of 16.3 months (range 0-45). As for cytogenetic analysis, 2 CDCs didn't grow in culture and in one case no karyotype alterations were reported. In the remaining 6 cases hypodiploid stemlines and a homogeneous chromosome alteration pattern were observed, with multiple numerical and structural aberrations (mean 11.1, range 7-15) and the continuous involvement of chromosomes 1 and X or Y, both as traslocation and deletion/monosomy. Additional abnormalities of chromosomes 22 and 13 were found to be common but less frequent. CONCLUSIONS: The clinical behaviour of the CDC is aggressive and its prognosis is surely poor; surgical treatment seems to be curative only for organ-confined cancer, accounting for the minority of cases. This neoplasm is cytogenetically characterized by hypodiploid stemlines with common involvement of chromosome 1 and the autosomes.


Subject(s)
Carcinoma, Renal Cell/pathology , Kidney Neoplasms/pathology , Kidney Tubules, Collecting , Aged , Aged, 80 and over , Carcinoma, Renal Cell/epidemiology , Carcinoma, Renal Cell/genetics , Cytogenetic Analysis , Female , Humans , Italy/epidemiology , Karyotyping , Kidney Neoplasms/epidemiology , Kidney Neoplasms/genetics , Male , Middle Aged , Prevalence
7.
Digestion ; 64(1): 1-8, 2001.
Article in English | MEDLINE | ID: mdl-11549831

ABSTRACT

BACKGROUND AND AIMS: A recent electron microscopy study suggested that dilated intercellular spaces (DIS) are specific for acid reflux-damaged esophageal epithelium. Electron microscopy is, however, expensive and difficult to apply to routine biopsies. The aims of this study are to establish a method for assessing DIS on light microscopy of esophageal biopsies and to estimate its association with current clinicopathological parameters of esophagitis. MATERIALS AND METHODS: 21 patients with reflux symptoms were investigated. Light microscopy biopsies were assessed for DIS size by a semiquantitative method and computer-assisted, static morphometry. A DIS score accounting for DIS size and distribution was assigned to each patient and its association with 30 clinicopathological variables investigated by univariate and multivariate logistic regression. RESULTS: Both the semiquantitative method and static morphometry identified 4 different classes of DIS size. The DIS score was significantly and independently associated with the esophageal symptoms score, the histological score of esophagitis and the relevant morphometry data. CONCLUSIONS: DIS may be efficiently assessed during light microscopy of routine esophageal biopsies. Since correlation with both the histology and the symptoms of esophagitis, the DIS score may be considered a novel parameter of esophagitis and is suggested for the routine evaluation of esophageal biopsies in patients with reflux disease.


Subject(s)
Esophagus/ultrastructure , Extracellular Space , Gastroesophageal Reflux/diagnosis , Mucous Membrane/pathology , Mucous Membrane/ultrastructure , Adult , Aged , Aged, 80 and over , Biopsy , Cell Count , Clinical Laboratory Techniques , Diagnosis, Computer-Assisted/methods , Esophagoscopy , Esophagus/pathology , Female , Gastroesophageal Reflux/classification , Humans , Logistic Models , Male , Microscopy, Video/methods , Middle Aged , Predictive Value of Tests
8.
Circulation ; 100(19): 1983-91, 1999 Nov 09.
Article in English | MEDLINE | ID: mdl-10556225

ABSTRACT

BACKGROUND: Cytokine activation and endothelial dysfunction are typical phenomena of congestive heart failure (CHF). We tested the hypothesis that incubating human umbilical vein endothelial cells with serum from patients with CHF will downregulate endothelial constitutive nitric oxide synthase (eNOS) and induce apoptosis. METHODS AND RESULTS: We studied 21 patients with severe CHF. Levels of tumor necrosis factor-alpha (TNF-alpha) and several neuroendocrine parameters were assessed. eNOS was measured by Western Blot analysis and apoptosis by optical microscopy and flow cytometry. We observed (1) eNOS downregulation (difference versus healthy subjects at 24 hours [P<0.05] and 48 hours [P<0.001]), (2) nuclear morphological changes typical of apoptosis; and (3) a high apoptotic rate with propidium iodide (increasing from 2.1+/-0.4% to 11.3+/-1.2% at 48 hours; P<0.001 versus healthy subjects) and annexin V. An anti-human TNF-alpha antibody did not completely counteract these effects. A strong correlation existed between eNOS downregulation and apoptosis (r = -0.89; P<0.001). CONCLUSIONS: Serum from patients with severe CHF downregulates eNOS expression and increases apoptosis. High levels of TNF-alpha likely play a role, but they cannot be the only factor responsible.


Subject(s)
Apoptosis , Heart Failure/blood , Nitric Oxide Synthase/antagonists & inhibitors , Tumor Necrosis Factor-alpha/physiology , Aged , Cells, Cultured , Down-Regulation , Endothelium, Vascular/physiology , Flow Cytometry , Humans , Middle Aged , Nitric Oxide Synthase/metabolism , Nitric Oxide Synthase Type III
9.
Pathologica ; 90(2): 120-6, 1998 Apr.
Article in Italian | MEDLINE | ID: mdl-9619054

ABSTRACT

UNLABELLED: The quantitation of DNA and growth fraction in the different step from dysplastic to neoplastic process in large bowel is the aim of this study. 70 colonic polyps were studied. The fresh specimens were processed and DNA analysis was carried out using a Partec CA II flow cytometer and the growth fraction was tested with KI-67 monoclonal antibody. The percentage of S-phase cells has been calculated with the Multicycle program. Our results demonstrated that 7 adenomas were tubulo-villous with mild dysplasia, 39 with mild-moderate dysplasia, 1 with severe dysplasia, 5 were polypoid carcinomas, 2 juvenile polyps, 1 polypoid leiomyoma, 1 inflammatory fibroid polyps. DNA analysis showed a diploid DNA content in non adenomatous polyps, in all adenomas with mild dysplasia, in 37 with mild-moderate dysplasia, in 8 cases with moderate-severe dysplasia and 1 cancer. Aneuploidy was discovered in 2 cases with mild-moderate dysplasia, in 6 cases with moderate-severe dysplasia, in the case of severe dysplasia and in 4 cases of carcinomas. Best indexes of linear correlation (Pearson's r) has been found between S-phase and DNA index (r = .75) and between S-phase and KI-67 (r = .82). IN CONCLUSION: 1) No relationship was found between DNA content and age, sex, size and location of polyps. 2) Aneuploidy is strictly related to moderate-severe grade of dysplasia therefore it is an important element in the development of adenomacarcinoma sequence. 3) DNA-index, S-phase and KI-67 are strictly related.


Subject(s)
Adenocarcinoma/pathology , Adenoma/pathology , Colonic Neoplasms/pathology , Colonic Polyps/pathology , DNA, Neoplasm/genetics , Flow Cytometry , Adenocarcinoma/genetics , Adenoma/genetics , Adult , Aged , Aged, 80 and over , Aneuploidy , Biomarkers, Tumor/analysis , Cell Cycle , Cell Nucleus/chemistry , Colonic Neoplasms/genetics , Colonic Polyps/genetics , Disease Progression , Female , Humans , Ki-67 Antigen/analysis , Leiomyoma/genetics , Leiomyoma/pathology , Male , Middle Aged , Neoplasm Invasiveness , Neoplasm Proteins/analysis
10.
Pathologica ; 89(2): 128-32, 1997 Apr.
Article in Italian | MEDLINE | ID: mdl-9411358

ABSTRACT

Cellular DNA content of solid tumors can be determined either from fresh, frozen, or formalin fixed, paraffin-embedded tissues. However, discordant results have been obtained using the paraffin-embedded technique, and lack of abnormal DNA stemlines in the paraffin-embedded as compared to either fresh or frozen tissues has been reported. In this study we evaluated the validity of nuclear extraction method from paraffin-embedded tissues, using 75 breast carcinomas whose DNA content was previously analyzed from frozen tissue and resulted either normal (12 cases) or abnormal (63 cases). From representative paraffin blocks, nuclei were extracted following Hedley's technique. The results revealed excellent cell counting and good histogram resolution from all paraffin samples; the loss of G2M abnormal peak in eight histograms with abnormal stemline did not compromise the correct interpretation of DNA content. In addition, the comparison between DNA indices obtained from corresponding paraffin and frozen samples showed a good correlation in 69 cases (r = 94); discordance in six cases was demonstrated to be related to tumor heterogeneity. In conclusion the paraffin extraction method is a sensible, and reliable technique, which can be applied for DNA flow cytometric studies on archival cases, as well as whenever fresh sample from the tumor is not obtainable.


Subject(s)
DNA/isolation & purification , Flow Cytometry , Frozen Sections , Paraffin Embedding , Aneuploidy , Breast Neoplasms/chemistry , Breast Neoplasms/pathology , Cell Count , Cell Nucleus/chemistry , DNA, Neoplasm/isolation & purification , False Negative Reactions , Female , G2 Phase , Humans , Metaphase , Pepsin A , Solvents , Tissue Fixation , Xylenes
13.
Cytometry ; 19(3): 263-6, 1995 Mar 01.
Article in English | MEDLINE | ID: mdl-7736871

ABSTRACT

Flow cytometric DNA analysis is an important prognostic tool in breast cancer. We evaluated the possibility of performing DNA analysis on cell suspensions obtained by scraping the cut surface of breast tumors; 31 breast tumor nodules, including six benign and 25 malignant lesions, were studied. From each case, cell suspensions acquired by mechanical mincing of a fresh frozen tissue fragment and by two different scrapings (central and peripheral) from the cut surface of the tumor were analyzed via flow cytometry. In all cases, comparison of the DNA histograms for three samples showed no significant differences in the appearance of debris or in the value of coefficient of variation of the G0-G1 peak. All benign nodules showed a normal DNA stemline in all specimens. In 23 of 25 cases of breast carcinoma, the ploidy of the three preparations was similar, with a concordance in 12/14 (85, 71%) cases in DNA nondiploid tumors. Linear regression analysis showed a good correlation in DNA index between either scraping sample and the tissue fragment (r = .955 and r = .905). The results indicate that the scraping technique provides excellent cell suspensions and DNA histograms comparable to those obtained from mechanical mincing of tissue fragments. The technique minimizes preparation time and avoids consuming much tissue and, thus, is the method of choice when very small cancers have to be analyzed.


Subject(s)
Biopsy/methods , Breast Neoplasms/chemistry , DNA, Neoplasm/analysis , Flow Cytometry/methods , Breast Neoplasms/pathology , Fibrocystic Breast Disease/chemistry , Fibrocystic Breast Disease/pathology , G1 Phase , Humans , Regression Analysis , Resting Phase, Cell Cycle
14.
Life Sci ; 56(16): 1311-20, 1995 Mar 10.
Article in English | MEDLINE | ID: mdl-8614252

ABSTRACT

Clinical and pharmacological evidence suggests that several neurotransmitters are involved in the control of the esophageal motility; in fact, besides the well known cholinergic and sympathetic innervation, Vasoactive Intestinal Polypeptide (VIP)-containing fibers as well as dopamine (DA)-containing nerve endings have been identified within the esophageal wall. Lower Esophageal Sphincter (LES) achalasia is a neuromuscular disorder characterized by the absence of peristalsis in the body of the esophagus and by the failure of the LES to relax in response to swallowing. Stimulation of both VIP receptors and D-2 DA receptors induce a decrease in LES pressure, while D-1 receptors mediates LES contractions. In the present study we show that both VIP and DA system is disregulated in LES achalasia. In particular, this disease is associated not only with the lack of VIP nerves in the LES, but also with a failure in the responsiveness of postsynaptic receptors to VIP stimulation. Furthermore, we demonstrate a selective functional loss of the D-2 DA receptor component, without changes in the D-1 DA receptor mediated responses.


Subject(s)
Esophageal Achalasia/etiology , Receptors, Dopamine/physiology , Receptors, Vasoactive Intestinal Peptide/physiology , Vasoactive Intestinal Peptide/physiology , Adenylyl Cyclases/metabolism , Cyclic AMP/biosynthesis , Esophageal Achalasia/physiopathology , Humans , S100 Proteins/analysis , Vasoactive Intestinal Peptide/analysis
15.
Eur Arch Otorhinolaryngol ; 252(6): 353-8, 1995.
Article in English | MEDLINE | ID: mdl-8679155

ABSTRACT

The DNA index, expression of cell-cycle-related proteins--proliferating cell nuclear antigen (PCNA, cyclin) and Ki-67--and the content of silver-binding nucleolar organizer regions (AgNORs) were evaluated in 30 unselected consecutive primary squamous cell carcinomas of the larynx. Results were compared and subsequently related to histological grading, lymph node status, pT category, and pathological stage. DNA content was non-diploid in 9 cases (30%). Mean AgNOR counts per tumor ranged from 2.52 to 8.76. PCNA and Ki-67 expressions were similar in 10 cases (33%). In the remaining cases, PCNA-positive cells usually outnumbered Ki-67-positive cells. No significant correlation was found among DNA index, PCNA and Ki-67 expressions, and AgNOR counts. Although there was a positive trend when Ki-67 was compared with histological grading, findings were not statistically significant. In contrast, a significant correlation was found between DNA index and lymph node status (P = 0.035), with a higher incidence of neck node metastases in non-diploid tumors. These data suggest that tumor ploidy can be correlated with lymph node spread in laryngeal squamous cell carcinoma and might be used as an additional prognostic factor when planning treatment.


Subject(s)
Carcinoma, Squamous Cell/genetics , Carcinoma, Squamous Cell/pathology , DNA, Neoplasm/analysis , Laryngeal Neoplasms/genetics , Laryngeal Neoplasms/pathology , Nucleolus Organizer Region/ultrastructure , Biomarkers, Tumor/analysis , Biomarkers, Tumor/genetics , Carcinoma, Squamous Cell/secondary , Carcinoma, Squamous Cell/ultrastructure , Cell Division/genetics , Coloring Agents , Cyclins/analysis , Cyclins/genetics , Diploidy , Female , Follow-Up Studies , Gene Expression Regulation, Neoplastic , Head and Neck Neoplasms/genetics , Head and Neck Neoplasms/pathology , Head and Neck Neoplasms/secondary , Humans , Incidence , Ki-67 Antigen , Laryngeal Neoplasms/ultrastructure , Lymph Nodes/pathology , Lymphatic Metastasis/genetics , Lymphatic Metastasis/pathology , Male , Neoplasm Proteins/analysis , Neoplasm Proteins/genetics , Neoplasm Staging , Nuclear Proteins/analysis , Nuclear Proteins/genetics , Nucleolus Organizer Region/genetics , Patient Care Planning , Ploidies , Prognosis , Proliferating Cell Nuclear Antigen/analysis , Proliferating Cell Nuclear Antigen/genetics , Silver
18.
Histopathology ; 19(2): 141-5, 1991 Aug.
Article in English | MEDLINE | ID: mdl-1757067

ABSTRACT

The monoclonal antibody KP1, which recognizes the CD 68 antigen on macrophages and myeloid precursors, was tested on 28 malignant (primary and metastatic) melanomas, 28 naevi, and 17 skin biopsies showing either normal (10) or hyperplastic melanocytes (7). Sixteen of 20 primary melanomas and six of eight metastatic melanomas showed variable numbers of KP1 positive tumour cells. All but five benign melanocytic proliferations (two Spitz naevi and three intradermal naevi), as well as normal and hyperplastic melanocytes were negative. These results indicate that difficulties may occur with the use of KP1 in the differential diagnosis between melanomas and neoplasms derived from histiocytes-macrophages, and that the expression of CD 68 antigen might be related to tumour progression in melanocytic cells.


Subject(s)
Antigens, CD/analysis , Melanoma/immunology , Nevus/immunology , Skin Neoplasms/immunology , Antibodies, Monoclonal/immunology , Biopsy , Humans , Melanoma/secondary , Skin Neoplasms/secondary
19.
Acta Otolaryngol ; 111(2): 437-43, 1991.
Article in English | MEDLINE | ID: mdl-2068933

ABSTRACT

The immunohistochemical localization of the basement membrane (BM) components laminin, type IV collagen and fibronectin was analyzed in normal, dysplastic and neoplastic laryngeal specimens. The distribution of these macromolecules was also investigated in metastatic lymph nodes. A regular and continuous staining for laminin and type IV collagen was present in normal and mild dysplastic epithelium (LIN I); interruptions and reduplications were more evident in severe dysplasia (LIN III), together with an increased positivity for fibronectin in the subepithelial connective tissue. In squamous cell carcinomas the distribution of BM components was related to the degree of cellular differentiation, with a decreased immunostaining being evident in moderately and poorly differentiated carcinomas. Furthermore, the positivity for laminin and type IV collagen was influenced by the pattern of neoplastic growth, being continuous around the "pushing" border and discontinuous where the neoplastic front had an "invading" appearance. Similar changes were present in cervical metastatic lymph nodes. These observations tend to support the theory that the neoplastic growth is a cyclic process, with BM component synthesis and reabsorbtion related to the shifts of cellular metabolism.


Subject(s)
Basement Membrane/chemistry , Carcinoma, Squamous Cell/chemistry , Laryngeal Neoplasms/chemistry , Larynx/chemistry , Lymph Nodes/chemistry , Antibodies, Monoclonal , Basement Membrane/pathology , Carcinoma, Squamous Cell/pathology , Cell Transformation, Neoplastic , Collagen/analysis , Fibronectins/analysis , Humans , Laminin/analysis , Laryngeal Neoplasms/pathology , Lymphatic Metastasis
20.
Minerva Med ; 81(10): 735-40, 1990 Oct.
Article in Italian | MEDLINE | ID: mdl-2234472

ABSTRACT

The clinical, radiographic and histological features of a case of eosinophilic gastritis in a 26 year old-man without personal or familial signs of allergy are reported. The Authors pointed out the importance of radiographic and histological aspects of the case studied. Therefore they represent essential methods for a correct diagnosis and an appropriate management that in this case is only pharmacological. The diagnosis of eosinophilic gastritis is, however, important for the recognition of specific allergens.


Subject(s)
Eosinophilia/pathology , Gastritis/pathology , Adult , Biopsy , Humans , Male
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