Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 3 de 3
Filter
Add more filters










Database
Language
Publication year range
1.
Epidemiology ; 12(6): 701-9, 2001 Nov.
Article in English | MEDLINE | ID: mdl-11679800

ABSTRACT

The t(14;18) translocation is a common somatic mutation in non-Hodgkin's lymphoma (NHL) that is associated with bcl-2 activation and inhibition of apoptosis. We hypothesized that some risk factors might act specifically along t(14;18)-dependent pathways, leading to stronger associations with t(14;18)-positive than t(14;18)-negative non-Hodgkin's lymphoma. Archival biopsies from 182 non-Hodgkin's lymphoma cases included in a case-control study of men in Iowa and Minnesota (the Factors Affecting Rural Men, or FARM study) were assayed for t(14;18) using polymerase chain reaction amplification; 68 (37%) were t(14;18)-positive. We estimated adjusted odds ratios (OR) and 95% confidence intervals (CI) for various agricultural risk factors and t(14;18)-positive and -negative cases of non-Hodgkin's lymphoma, based on polytomous logistic regression models fit using the expectation-maximization (EM) algorithm. T(14;18)-positive non-Hodgkin's lymphoma was associated with farming (OR 1.4, 95% CI = 0.9-2.3), dieldrin (OR 3.7, 95% CI = 1.9-7.0), toxaphene (OR 3.0, 95% CI = 1.5-6.1), lindane (OR 2.3, 95% CI = 1.3-3.9), atrazine (OR 1.7, 95% CI = 1.0-2.8), and fungicides (OR 1.8, 95% CI = 0.9-3.6), in marked contrast to null or negative associations for the same self-reported exposures and t(14;18)-negative non-Hodgkin's lymphoma. Causal relations between agricultural exposures and t(14;18)-positive non-Hodgkin's lymphoma are plausible, but associations should be confirmed in a larger study. Results suggest that non-Hodgkin's lymphoma classification based on the t(14;18) translocation is of value in etiologic research.


Subject(s)
Agricultural Workers' Diseases/genetics , Chromosomes, Human, Pair 14/drug effects , Chromosomes, Human, Pair 18/drug effects , Lymphoma, Non-Hodgkin/genetics , Translocation, Genetic/genetics , Adult , Aged , Agricultural Workers' Diseases/chemically induced , Agricultural Workers' Diseases/epidemiology , Agrochemicals/adverse effects , Algorithms , Apoptosis/genetics , Case-Control Studies , Chromosomes, Human, Pair 14/genetics , Chromosomes, Human, Pair 18/genetics , Confidence Intervals , Genes, bcl-2/genetics , Humans , Hydrocarbons, Chlorinated/adverse effects , Iowa/epidemiology , Lymphoma, Non-Hodgkin/chemically induced , Lymphoma, Non-Hodgkin/epidemiology , Male , Middle Aged , Minnesota/epidemiology , Odds Ratio , Polymerase Chain Reaction/methods , Risk Factors
2.
Histopathology ; 28(4): 317-23, 1996 Apr.
Article in English | MEDLINE | ID: mdl-8732340

ABSTRACT

High levels of bcl-2 protein have been found in a wide variety of human cancers. Since p53 gene inactivation occurs in over half of human cancers, it is possible that loss of p53-mediated repression of bcl-2 gene expression accounts, at least in part, for the frequent abnormalities in bcl-2 protein production seen in tumours. By using immunohistochemical methods, we have analysed thirty-three nasopharyngeal carcinomas for p53 and bcl-2 expression. We found an inverse correlation between the expression of these two proteins (P < 0.001). Moreover, we utilized universal oligonucleotide primers of a region 5' to the bcl-2 MBR and at the 3' end of JH segments to initiate a DNA polymerase chain reaction that amplified these bcl-2-JH junctures. Of the twelve nasopharyngeal carcinomas expressing bcl-2, none showed a t(14;18) chromosome translocation. These findings may indicate potential mechanisms by which bcl-2 regulates apoptosis.


Subject(s)
Carcinoma/genetics , Chromosomes, Human, Pair 14/drug effects , Chromosomes, Human, Pair 18/drug effects , Down-Regulation/genetics , Nasopharyngeal Neoplasms/genetics , Proto-Oncogene Proteins c-bcl-2/drug effects , Translocation, Genetic/drug effects , Tumor Suppressor Protein p53/pharmacology , Base Sequence , Down-Regulation/drug effects , Humans , Molecular Sequence Data , Tissue Fixation , Tumor Suppressor Protein p53/biosynthesis , Tumor Suppressor Protein p53/immunology
3.
Article in English | MEDLINE | ID: mdl-1303128

ABSTRACT

Appliers of pesticides (n = 18) who are exposed to the fumigant phosphine or who have a mixed exposure to other pesticides and phosphine demonstrate a significant increase in chromosome rearrangements in G-banded chromosomes from peripheral blood compared to control subjects (n = 26). Appliers who had discontinued using phosphine for at least 8 months prior to specimen collection (n = 5) do not demonstrate significant increases in chromosome rearrangements compared to controls. Breakpoint analysis of 6,138 metaphases from all subjects demonstrates 196 breaks per 3605 metaphases in exposed subjects and 102 breaks per 2,533 metaphases in control subjects. Bands with significantly more breaks than expected based on band length in all study subjects were 1q32, 3p14, 7p15, and 14q11. Three of these four bands had significantly more breaks than expected in the exposed group, and all four bands had a significant excess of breaks in the control group. There are four bands with a significant excess of breaks in the exposed group and no breaks in the control group; each of these occurs in a known protooncogene region. These are 1p13 (NRAS), 2p23 (NMYC), 14q32 (ELK2), and 21q12 (ETS-2). Most breaks at bands 1p13, 14q32, and 21q22 are associated with chromosome rearrangements and occurred in appliers who have a mixed exposure to phosphine and other pesticides. Cytogenetic abnormalities, i.e., rearrangements and/or deletions involving bands 1p13, 2p23, and 14q32, are associated with non-Hodgkin's lymphoma. We speculate that these findings could relate to the risk of evolution of a neoplastic clone in these workers. Epidemiological studies of similarly exposed workers indicate an excess of non-Hodgkin's lymphoma.


Subject(s)
Gene Rearrangement/drug effects , Insecticides/adverse effects , Lymphoma, Non-Hodgkin/chemically induced , Occupational Diseases/chemically induced , Occupational Exposure , Phosphines/adverse effects , Chromatids/drug effects , Chromosome Aberrations , Chromosomes/drug effects , Chromosomes, Human, Pair 1/drug effects , Chromosomes, Human, Pair 14/drug effects , Follow-Up Studies , Humans , Karyotyping , Lymphoma, Non-Hodgkin/genetics , Male , Metaphase , Occupational Diseases/genetics , Pesticides/adverse effects , Risk Factors , Time Factors , Translocation, Genetic/drug effects
SELECTION OF CITATIONS
SEARCH DETAIL
...