ABSTRACT
SGN-30, a monoclonal antibody with activity against CD30+ malignancies, is currently in phase II clinical evaluation for treatment of Hodgkin's disease (HD) and anaplastic large cell lymphoma. The mechanisms underlying SGN-30's antitumor activity were investigated using cDNA array of L540 cells. SGN-30 treatment activated NF-kappaB and modulation of several messages including the growth regulator p21WAF1/CIP1 (p21) and cellular adhesion marker ICAM-1. p21 protein levels increased coincident with growth arrest and Annexin V/PI staining in treated HD cells. To determine if SGN-30-induced growth arrest would sensitize tumor cells to chemotherapeutics used against HD, L540cy and L428 cells were exposed to SGN-30 in combination with a panel of cytotoxic agents and resultant interactions quantified by the Combination Effects Method. Interactions between SGN-30 and all cytotoxic agents examined were additive or better. These in vitro data translated to increased efficacy of SGN-30 and bleomycin against L540cy tumor xenografts. In addition to direct cell killing, SGN-30 affects growth arrest and drug sensitization through growth regulating and proapoptotic machinery. Importantly, these data suggest that SGN-30 can enhance the efficacy of standard chemotherapies used to treat patients with CD30+ malignancies.
Subject(s)
Antibodies, Monoclonal/therapeutic use , Hodgkin Disease/drug therapy , Hodgkin Disease/immunology , Ki-1 Antigen/immunology , Signal Transduction/immunology , Animals , Antibodies, Monoclonal/immunology , Apoptosis/drug effects , Bleomycin/therapeutic use , Cell Cycle/drug effects , Cell Cycle/immunology , Cell Line, Tumor , Drug Therapy, Combination , Hodgkin Disease/genetics , Humans , Ki-1 Antigen/drug effects , Mice , Mice, SCID , NF-kappa B/drug effects , NF-kappa B/immunology , Oligonucleotide Array Sequence Analysis/methods , Sensitivity and Specificity , Signal Transduction/drug effects , Xenograft Model Antitumor Assays/methodsSubject(s)
Gene Expression , Colorectal Neoplasms/genetics , Female , Genome, Human , Humans , Male , Neoplasms/genetics , Tissue Distribution , Tumor Cells, CulturedABSTRACT
Several methods have been used recently to determine gene expression profiles of cell populations. Here we demonstrate the strength of combining two approaches, serial analysis of gene expression (SAGE) and DNA arrays, to help elucidate pathways in breast cancer progression by finding genes consistently expressed at different levels in primary breast cancers, metastatic breast cancers, and normal mammary epithelial cells. SAGE profiles of 21PT and 21MT, two well-characterized breast tumor cell lines, were compared with SAGE profiles of normal breast epithelial cells to identify differentially expressed genes. A subset of these candidates was then placed on an array and screened with clinical breast tumor samples to find genes and expressed sequence tags that are consistently expressed at different levels in diseased and normal tissues. In addition to finding the predicted overexpression of known breast cancer markers HER-2/neu and MUC-1, the powerful coupling of SAGE and DNA arrays resulted in the identification of genes and potential pathways not implicated previously in breast cancer. Moreover, these techniques also generated information about the differences and similarities of expression profiles in primary and metastatic breast tumors. Thus, combining SAGE and custom array technology allowed for the rapid identification and validation of the clinical relevance of many genes potentially involved in breast cancer progression. These differentially expressed genes may be useful as tumor markers and prognostic indicators and may be suitable targets for various forms of therapeutic intervention.
Subject(s)
Breast Neoplasms/genetics , DNA Mutational Analysis/methods , Gene Expression Regulation, Neoplastic/genetics , Oligonucleotide Array Sequence Analysis , Biomarkers, Tumor/metabolism , Breast Neoplasms/pathology , DNA, Complementary/analysis , Female , Gene Library , Humans , RNA, Messenger/analysis , Transcription, Genetic , Tumor Cells, CulturedABSTRACT
Enterococcus faecium has recently emerged as a serious nosocomial pathogen. The prevalence and severity of enterococcal infections, the mortality rate from such infections, and the antibiotic resistance of enterococci are often species dependent. Since conventional biochemical methods fail to differentiate E. faecium from certain newly described enterococcal species, a PCR-based assay was developed for the rapid identification of E. faecium.
Subject(s)
Enterococcus faecium/isolation & purification , Polymerase Chain Reaction/methods , Molecular Sequence DataABSTRACT
A polymerase chain reaction (PCR)-based assay was developed for the detection of Mycoplasma hominis. This assay generates a 152-bp PCR product which was part of an initial 471-bp M. hominis genomic DNA fragment. The 471-bp DNA fragment was shown by hybridization analysis to be unique for M. hominis. The PCR assay can amplify as few as 18 molecules of target DNA. This diagnostic assay offers potential for wide clinical application as it is rapid and can be successfully performed on crude sample preparations from a variety of media or biopsies. The use of this assay should aid in defining the aetiologic and pathologic roles played by M. hominis and thereby benefit patients.
Subject(s)
DNA, Bacterial/analysis , Mycoplasma Infections/microbiology , Mycoplasma/isolation & purification , Polymerase Chain Reaction/methods , Adult , Base Sequence , DNA Probes , DNA, Bacterial/genetics , Female , Humans , Infant, Newborn , Male , Molecular Sequence Data , Mycoplasma/classification , Mycoplasma/genetics , Mycoplasma Infections/diagnosis , Pregnancy , Pregnancy Complications, Infectious/microbiology , Respiratory Tract Infections/microbiology , Sensitivity and Specificity , Species Specificity , Specimen Handling , Urethritis/microbiology , Vaginosis, Bacterial/microbiologyABSTRACT
Methicillin resistance in Staphylococcus aureus is a frequent cause of nosocomial and community-acquired infections. Accurate, rapid epidemiologic typing is crucial to the identification of the source and spread of infectious disease and could provide detailed information on the generation of methicillin-resistant S. aureus (MRSA) strains. The high degree of genetic relatedness of MRSA strains has precluded the use of more conventional methods of genetic fingerprinting. A rapid DNA fingerprinting method that exploits PCR amplification from a DNA repeat sequence in MRSA is described. The random chromosomal distribution of this repeat sequence provides an ideal target for detecting DNA fragment patterns specific to individual MRSA strains. Two PCR fingerprinting methods which use an oligonucleotide primer based on a repetitive sequence found in Mycoplasma pneumoniae are presented. The repetitive element sequence-based PCR (rep-PCR) and fluorophore-enhanced rep-PCR (FERP) can identify epidemic strains among background MRSA. The combination of oligonucleotide primers labeled with different fluorescent dyes allowed simultaneous FERP fingerprinting and mecA gene detection. Eight different fingerprint patterns were observed in MRSA strains collected from different sources. These techniques provide a rapid discriminatory means of molecular epidemiologic typing of MRSA involved in nosocomial infections.