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1.
Hum Pathol ; 46(9): 1275-81, 2015 Sep.
Article in English | MEDLINE | ID: mdl-26170010

ABSTRACT

Oral squamous cell carcinoma (OSCC) is the most common oral cancer, and major efforts is being made to identify molecular markers capable to differentiate oral potentially malignant lesions (OPMLs) with indolent course from lesions with aggressive behavior. We undertook a study to evaluate if gain of the human telomerase RNA component (hTERC) gene in OPMLs could indicate lesions at high risk of developing OSCC. The study was performed on 30 OPMLs with long-term follow-up using a dual-color interphase fluorescence in situ hybridization (FISH) for hTERC status. Progression to malignancy was observed in 9 of 10 cases harboring hTERC gain and in 1 of 20 cases retaining a normal copy number of hTERC (P < .0001). Combining morphological grading and FISH analysis, all the cases with high-grade squamous intraepithelial lesion or carcinoma in situ harboring hTERC amplification progressed to OSCC, whereas none of the low-grade squamous intraepithelial lesions without hTERC gain progressed. Intermediate situations occurred. The data suggest that precise morphological evaluation together with FISH assessment for hTERC gain might pave the way to stratify OPMLs into high-risk and low-risk categories and could be helpful in selecting the most appropriate treatment.


Subject(s)
Biomarkers, Tumor/genetics , Carcinoma in Situ/genetics , Carcinoma, Squamous Cell/genetics , Gene Amplification , Head and Neck Neoplasms/genetics , In Situ Hybridization, Fluorescence , Mouth Neoplasms/genetics , Precancerous Conditions/genetics , RNA/genetics , Telomerase/genetics , Adult , Aged , Aged, 80 and over , Carcinoma in Situ/enzymology , Carcinoma in Situ/mortality , Carcinoma in Situ/pathology , Carcinoma, Squamous Cell/enzymology , Carcinoma, Squamous Cell/mortality , Carcinoma, Squamous Cell/pathology , Disease Progression , Female , Head and Neck Neoplasms/enzymology , Head and Neck Neoplasms/mortality , Head and Neck Neoplasms/pathology , Humans , Kaplan-Meier Estimate , Male , Middle Aged , Mouth Neoplasms/enzymology , Mouth Neoplasms/mortality , Mouth Neoplasms/pathology , Neoplasm Grading , Precancerous Conditions/enzymology , Precancerous Conditions/mortality , Precancerous Conditions/pathology , Predictive Value of Tests , Risk Assessment , Risk Factors , Squamous Cell Carcinoma of Head and Neck , Time Factors
2.
Am J Obstet Gynecol ; 213(1): 51.e1-51.e8, 2015 Jul.
Article in English | MEDLINE | ID: mdl-25659466

ABSTRACT

OBJECTIVE: Chromosome 3q gain has been consistently observed in cervical intraepithelial neoplasia grades 2 and 3 (CIN 2,3) and squamous cell carcinomas of the cervix. There are a number of potential clinical uses of testing for 3q gain in liquid cytology specimens, including the identification of subsets of women with atypical squamous cells of undetermined significance or low-grade squamous intraepithelial lesion cytology who are at greatest risk of having CIN 2,3 and would thus benefit most from immediate colposcopy. The objective of this study was to establish the sensitivity and specificity of 3q gain for discriminating between CIN 2,3 and normal. STUDY DESIGN: Residual cytology specimens were collected from 199 women. Liquid-based cytology (LBC) was used for the selection of subjects, with women with high-grade squamous intraepithelial lesion or high-grade squamous intraepithelial lesion who had colposcopy and adjudicated biopsy-confirmed CIN 2,3 forming the disease-positive group (n = 28) and women doubly negative for both cytology and high-risk human papillomavirus (hrHPV) testing forming the disease-negative group (n = 171). A single slide was prepared from each residual LBC specimen and analyzed for 3q gain by fluorescent in situ hybridization, using a probe specific for the 3q26 region and a control probe for the chromosome 7 centromere. Two approaches were compared for the determination of 3q gain. The first was based on the analysis of an entire cervical cytology slide for the presence of rare cells with a high copy number (>4 copies) for the 3q locus. The second approach was based on the analysis of 400 cells to determine the percentage with 3 or more copies of the 3q locus. RESULTS: Using the approach based on the detection of rare cells with a high copy number (>4 copies) for the 3q locus, 26 of the specimens from women with CIN 2,3 and none of the 171 specimens from women who were both hrHPV and cytology negative was positive for 3q gain. This translates to a sensitivity of 92.9% (95% confidence interval [CI], 76.5-98.9%), a specificity of 100% (95% CI, 97.8-100%), a positive predictive value of 100% (95% CI, 86.7-100%), and a negative predictive value of 98.8% (95% CI, 95.9-99.8), for distinguishing CIN 2,3 from normal. CONCLUSION: These data support the potential clinical use of 3q gain for the evaluation of women in a number of clinical situations, including women with atypical squamous cells of undetermined significance, low-grade squamous intraepithelial lesion, and those who are hrHPV positive.


Subject(s)
Chromosomes, Human, Pair 3/genetics , Precancerous Conditions/genetics , Uterine Cervical Dysplasia/genetics , Uterine Cervical Neoplasms/genetics , Algorithms , Atypical Squamous Cells of the Cervix , DNA Probes , Female , Gene Dosage , Humans , In Situ Hybridization, Fluorescence , Sensitivity and Specificity , Squamous Intraepithelial Lesions of the Cervix/genetics
3.
Exp Mol Pathol ; 98(1): 113-8, 2015 Feb.
Article in English | MEDLINE | ID: mdl-25576649

ABSTRACT

In the past several years we have observed a significant increase in our understanding of molecular mechanisms that drive lung cancer. Specifically in the non-small cell lung cancer sub-types, ALK gene rearrangements represent a sub-group of tumors that are targetable by the tyrosine kinase inhibitor Crizotinib, resulting in significant reductions in tumor burden. Phase II and III clinical trials were performed using an ALK break-apart FISH probe kit, making FISH the gold standard for identifying ALK rearrangements in patients. FISH is often considered a labor and cost intensive molecular technique, and in this study we aimed to demonstrate feasibility for automation of ALK FISH testing, to improve laboratory workflow and ease of testing. This involved automation of the pre-treatment steps of the ALK assay using various protocols on the VP 2000 instrument, and facilitating automated scanning of the fluorescent FISH specimens for simplified enumeration on various backend scanning and analysis systems. The results indicated that ALK FISH can be automated. Significantly, both the Ikoniscope and BioView system of automated FISH scanning and analysis systems provided a robust analysis algorithm to define ALK rearrangements. In addition, the BioView system facilitated consultation of difficult cases via the internet.


Subject(s)
Carcinoma, Non-Small-Cell Lung/genetics , Data Interpretation, Statistical , Gene Rearrangement , In Situ Hybridization, Fluorescence/methods , Lung Neoplasms/genetics , Receptor Protein-Tyrosine Kinases/genetics , Algorithms , Anaplastic Lymphoma Kinase , Automation , Carcinoma, Non-Small-Cell Lung/drug therapy , Carcinoma, Non-Small-Cell Lung/pathology , Clinical Trials, Phase II as Topic , Clinical Trials, Phase III as Topic , Crizotinib , Feasibility Studies , Humans , Lung Neoplasms/drug therapy , Lung Neoplasms/pathology , Neoplasm Staging , Prognosis , Protein Kinase Inhibitors/therapeutic use , Pyrazoles/therapeutic use , Pyridines/therapeutic use , Software
4.
ScientificWorldJournal ; 2012: 349597, 2012.
Article in English | MEDLINE | ID: mdl-22629135

ABSTRACT

Urinary tract infections (UTIs) are among the most frequent community-acquired infections worldwide. Escherichia coli is the most common UTI pathogen although underlying host factors such as patients' age and gender may influence prevalence of causative agents. In this study, 61 273 consecutive urine samples received over a 22-month period from outpatients clinics of an urban area of north Italy underwent microbiological culture with subsequent bacterial identification and antimicrobial susceptibility testing of positive samples. A total of 13 820 uropathogens were isolated and their prevalence analyzed according to patient's gender and age group. Overall Escherichia coli accounted for 67.6% of all isolates, followed by Klebsiella pneumoniae (8.8%), Enterococcus faecalis (6.3%), Proteus mirabilis (5.2%), and Pseudomonas aeruginosa (2.5%). Data stratification according to both age and gender showed E. coli isolation rates to be lower in both males aged ≥60 years (52.2%), E. faecalis and P. aeruginosa being more prevalent in this group (11.6% and 7.8%, resp.), as well as in those aged ≤14 years (51.3%) in whom P. mirabilis prevalence was found to be as high as 21.2%. Streptococcus agalactiae overall prevalence was found to be 2.3% although it was shown to occur most frequently in women aged between 15 and 59 years (4.1%). Susceptibility of E. coli to oral antimicrobial agents was demonstrated to be as follows: fosfomycin (72.9%), trimethoprim/sulfamethoxazole (72.9%), ciprofloxacin (76.8%), ampicillin (48.0%), and amoxicillin/clavulanate (77.5%). In conclusion, both patients' age and gender are significant factors in determining UTIs etiology; they can increase accuracy in defining the causative uropathogen as well as providing useful guidance to empiric treatment.


Subject(s)
Bacterial Infections/epidemiology , Community-Acquired Infections/epidemiology , Urinary Tract Infections/epidemiology , Adolescent , Adult , Age Distribution , Causality , Female , Humans , Italy/epidemiology , Male , Middle Aged , Prevalence , Risk Assessment , Risk Factors , Sex Distribution , Young Adult
5.
Dig Liver Dis ; 44(6): 461-5, 2012 Jun.
Article in English | MEDLINE | ID: mdl-22285147

ABSTRACT

BACKGROUND: Specific bacterial infections or alterations of the gut microbiota likely trigger immuno-pathological phenomena associated with Crohn's disease and ulcerative colitis. Mycobacterium avium subspecies paratuberculosis is a candidate etiological agent of Crohn's disease. Definitive causal connection between Mycobacterium avium subspecies paratuberculosis infection and Crohn's disease has not been demonstrated. AIMS: To determine the circulation of Mycobacterium avium subspecies paratuberculosis in Crohn's disease patients and water supplies in an Italian region where this bacterium is endemic in cattle farms. METHODS: Mycobacterium avium subspecies paratuberculosis screening was performed on biopsies from human patients, and from water samples, using two different PCR procedures. RESULTS: In hospitals where multiple specimens were obtained from different sites in the intestine, the prevalence of Mycobacterium avium subspecies paratuberculosis infection was 82.1% and 40% respectively in Crohn's disease and ulcerative colitis patients; in another hospital, where single specimens were obtained from patients, the bacterium was not detected. Control subjects also harboured Mycobacterium avium subspecies paratuberculosis, but at a lower prevalence. Tap water samples collected in the study area contained Mycobacterium avium subspecies paratuberculosis DNA. DISCUSSION: The results of screenings for Mycobacterium avium subspecies paratuberculosis in humans are deeply influenced by both the number and location of the collected biopsies. There is a wide circulation of the organism in the study area, considering the prevalence in humans and its presence in drinking water.


Subject(s)
Crohn Disease/microbiology , DNA, Bacterial/isolation & purification , Drinking Water/microbiology , Mycobacterium avium subsp. paratuberculosis/isolation & purification , Paratuberculosis/epidemiology , Chi-Square Distribution , Colitis, Ulcerative/microbiology , Humans , Intestines/microbiology , Italy/epidemiology , Paratuberculosis/complications , Prevalence
7.
Clin Chem Lab Med ; 40(2): 167-73, 2002 Feb.
Article in English | MEDLINE | ID: mdl-11939491

ABSTRACT

This study was undertaken to evaluate the feasibility of using commercial control materials in a regional external quality assessment scheme (EQAS) for serum carcinoembryonic antigen (CEA) measurement. We have assessed the commutability of 12 commercial control materials using five automated immunochemical systems. We compared the intermethod behavior of the materials with that of 12-14 patient serum pools. In a total of 48 comparisons (12 materials x 4 pairs of analytical systems), seven instances of non-commutability were apparent, as shown by normalized residuals falling outside the +/-3 interval. The use of non-commutable materials generates two negative effects. In EQAS, the interlaboratory variation recorded is not representative of the variation expected in the assay of patient sera; in interlaboratory harmonization programs, recalibration with non-commutable materials increases, instead of decreasing, the interlaboratory variation. Both these effects were shown to occur in CEA measurement with the tested materials and systems. The materials planned to be used in our EQAS turned out to be commutable: this gave us the guarantee of measuring realistic interlaboratory variation values, although the check for commutability should be extended to all the analytical systems used by the participants in the scheme.


Subject(s)
Carcinoembryonic Antigen/blood , Calibration , Humans , Reference Standards , Reproducibility of Results
8.
Rev. bras. anal. clin ; 22(1): 6-8, mar. 1990. tab
Article in Portuguese | LILACS | ID: lil-124765

ABSTRACT

Os autores examinaram uma amostra de 124 pacientes afetados por hemoglobinopatias a fim de individualizar a freqüência relativa de tais desordens e a sensibilidade diagnóstica dos testes comumente empregados em laboratório considerado de priméiro nível


Subject(s)
Humans , Hemoglobinopathies/prevention & control , Hemoglobins/genetics , Brazil
9.
Rev. bras. anal. clin ; 21(2): 45-7, 1989. tab
Article in Portuguese | LILACS | ID: lil-135536

ABSTRACT

Os hormonios esteroidianos podem interferir na dosagem imunologica da digoxinemia. Neste trabalho, os autores avaliam a influencia de cinco hormonios esteroidianos sobre a especificidade analitica e diagnostica de quatro metodos da rotina para a dosagem da digoxina plasmatica


Subject(s)
Humans , Digoxin , Hormones/analysis
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