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1.
Tumour Biol ; 37(8): 11115-26, 2016 Aug.
Article in English | MEDLINE | ID: mdl-26912061

ABSTRACT

In this study, we analyzed the expression profile of four genes (CCNA2, CCNB1, CCNB2, and CDK1) in laryngeal squamous cell carcinoma (LSCC) cell lines and tumor samples. With the application of microarray platform, we have shown the overexpression of these genes in all analyzed LSCC samples in comparison to non-cancer controls from head and neck region. We have selected CDK1 for further analysis, due to its leading role in cell cycle regulation. It is a member of the Ser/Thr protein kinase family of proven oncogenic properties. The results obtained for CDK1 were further confirmed with the application of reverse transcription quantitative polymerase chain reaction (RT-qPCR) technique, Western blot, and immunohistochemistry (IHC). The observed upregulation of CDK1 in laryngeal squamous cell carcinoma has encouraged us to analyze for genetic mechanisms that can be responsible this phenomenon. Therefore, with the application of array-CGH, sequencing analysis and two methods for epigenetic regulation analysis (DNA methylation and miRNA expression), we tried to identify such potential mechanisms. Our attempts to identify the molecular mechanisms responsible for observed changes failed as we did not observe significant alterations neither in the DNA sequence nor in the gene copy number that could underline CDK1 upregulation. Similarly, the pyrosequencing and miRNA expression analyses did not reveal any differences in methylation level and miRNA expression, respectively; thus, these mechanisms probably do not contribute to elevation of CDK1 expression in LSCC. However, our results suggest that alteration of CDK1 expression on both mRNA and protein level probably appears on the very early step of carcinogenesis.


Subject(s)
Carcinoma, Squamous Cell/genetics , Cyclin-Dependent Kinases/biosynthesis , Head and Neck Neoplasms/genetics , Laryngeal Neoplasms/genetics , Neoplasm Recurrence, Local/genetics , Adult , Aged , Aged, 80 and over , Biomarkers, Tumor/analysis , Biomarkers, Tumor/genetics , Blotting, Western , CDC2 Protein Kinase , Carcinoma, Squamous Cell/pathology , Cell Line, Tumor , Cyclin-Dependent Kinases/analysis , Female , Head and Neck Neoplasms/pathology , Humans , Immunohistochemistry , Laryngeal Neoplasms/pathology , Male , Middle Aged , Neoplasm Recurrence, Local/pathology , Oligonucleotide Array Sequence Analysis , Polymerase Chain Reaction , Squamous Cell Carcinoma of Head and Neck , Transcriptome , Up-Regulation
2.
Pol J Vet Sci ; 14(4): 679-81, 2011.
Article in English | MEDLINE | ID: mdl-22439345

ABSTRACT

Real-time PCR directed to intergenic spacer (IGS) noncoding region between 16S and 23S rRNA genes was used for species specific detection of Mycoplasma felis in conjunctival scrapings. Samples were collected from 57 cats suffering from chronic conjunctivitis in 2008-2010 (Wroclaw, Poland). Samples from 36 cats (63.2%) were shown to be positive for Mycoplasma felis. Our research gives a first insight in the occurrence of Mycoplasma felis among domestic cats in Poland suggesting that this pathogen may constitute an underestimated cause of chronic conjunctivitis.


Subject(s)
Cat Diseases/microbiology , Conjunctivitis, Bacterial/veterinary , Mycoplasma Infections/veterinary , Mycoplasma/classification , Real-Time Polymerase Chain Reaction/veterinary , Animals , Cat Diseases/epidemiology , Cats , Chronic Disease , Conjunctivitis, Bacterial/epidemiology , Conjunctivitis, Bacterial/microbiology , Mycoplasma/isolation & purification , Mycoplasma Infections/epidemiology , Mycoplasma Infections/microbiology , Poland/epidemiology
3.
Cancer Detect Prev ; 18(1): 65-78, 1994.
Article in English | MEDLINE | ID: mdl-8162608

ABSTRACT

The serum anti-malignin antibody (AMA) test determines the antibody to malignin, a 10,000-Da peptide present in patients with a wide variety of cancers. A total of 3315 double-blind tests demonstrated that AMA is a general transformation antibody, elevated in active nonterminal cancer, regardless of the site or tissue type, with sensitivity and specificity of 95% on the first determination and > 99% on repeat determinations. Data have not however been published yet that indicate whether, in daily clinical practice, the AMA test provides accurate prospective and predictive information. Forty-two physicians from 11 states, who ordered the AMA test, performed blind, report here on their results on 208 determinations in the first consecutive 181 patients and controls. Used in monitoring treatment in 56 patients, the test predicted or agreed 94.1% overall with the clinical status. Used in early detection in 125 patients and controls, of which 118 now have confirmed diagnoses, AMA was elevated in 21, all of whom were proven to have cancer; AMA was normal in 97, none of whom had cancer. Transient elevated AMA occurred in 3%, followed by normal values. Seven patients with still uncertain diagnosis who have had elevated AMA on repeated tests for 1 year or longer include six who are symptomatic, and three whose families have a high frequency of cancer. The conditions of these 7 may include undetected cancer because of the 118 with now certain diagnosis the AMA test predicted all correctly. From our experience, the AMA test should be used together with other routine procedures whenever signs and symptoms suggest cancer to facilitate early detection.


Subject(s)
Antibodies/analysis , Antigens, Neoplasm/immunology , Neoplasm Proteins/immunology , Neoplasms/diagnosis , Adult , Aged , Aged, 80 and over , Biomarkers, Tumor/analysis , Female , Humans , Male , Middle Aged , Neoplasms/mortality , Survival Rate
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