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1.
Am J Pathol ; 159(4): 1495-505, 2001 Oct.
Article in English | MEDLINE | ID: mdl-11583976

ABSTRACT

To investigate the lymphomagenesis of NK/T lymphoma, we comprehensively and systematically analyzed the expression pattern of the human NK/T cell line (NK-YS) genome by cDNA expression array and tissue microarray. We detected significant changes in the gene expression of NK-YS cell line: an increase in 18 and a decrease in 20 genes compared to normal NK cells or peripheral blood mononuclear cells. Among these genes, we found a strong decrease in hematopoietic cell specific protein-tyrosine-phosphatase SH-PTP1 (SHP1) mRNA by cDNA expression array and reverse transcriptase-polymerase chain reaction. Further analysis with standard immunohistochemistry and tissue microarray, which used 207 paraffin-embedded specimens of various kinds of malignant lymphomas, showed that 100% of NK/T lymphoma specimens and more than 95% of various types of malignant lymphoma were negative for SHP1 protein expression. On the other hand, SHP1 protein was strongly expressed in the mantle zone and interfollicular zone lymphocytes in reactive lymphoid hyperplasia specimens. In addition, various kinds of hematopoietic cell lines, particularly the highly aggressive lymphoma/leukemia lines, lacked SHP1 expression in vitro, suggesting that loss of SHP1 expression may be related to not only malignant transformation, but also tumor cell aggressiveness. SHP1 expression could not be induced in either of two NK/T cell lines by phorbol ester, suggesting that genetic impairment or modification with methylation of SHP1 DNA could be one of the critical events in the pathogenesis of NK/T lymphoma. This evidence strongly suggests that loss of SHP1 gene expression plays an important role in multistep tumorigenesis, possibly as an anti-oncogene in the wide range of lymphomas/leukemias as well as NK/T lymphomas.


Subject(s)
Gene Expression , Hematopoietic Stem Cells/enzymology , Killer Cells, Natural/pathology , Leukemia/genetics , Lymphoma/genetics , Lymphoma/pathology , DNA, Complementary/genetics , Gene Expression Profiling , Humans , Oligonucleotide Array Sequence Analysis , Pseudolymphoma/genetics , RNA, Messenger/metabolism , Reference Values , Tumor Cells, Cultured
2.
Biol Pharm Bull ; 20(5): 547-55, 1997 May.
Article in English | MEDLINE | ID: mdl-9178937

ABSTRACT

In a previous paper, we reported that an extract of silkworm faeces has a marked antiviral activity on enveloped viruses, but not on a non-enveloped virus, and we showed that it inhibits the synthesis of a viral specific gene of HVJ (Sendai virus) without affecting the viral adsorption and entry into the host cell. In this paper, we accomplished the purification of an antiviral active substance by extraction of a hydrophobic substance and thin layer chromatography. The active substance was found to be a chlorophyll-like substance with a molecular mass of about 530. This substance shows clear antiviral activity against HVJ, HSV (herpes simplex virus type-1), and HIV (human immunodeficiency virus type-1). Its antiviral activity was dependent on light irradiation and temperature. Furthermore, it also possesses a strong hemolytic activity under light.


Subject(s)
Antiviral Agents/isolation & purification , Antiviral Agents/pharmacology , Bombyx/chemistry , Chlorophyll/isolation & purification , Chlorophyll/pharmacology , Glycoproteins/isolation & purification , Glycoproteins/pharmacology , Animals , Antiviral Agents/radiation effects , Cell Line , Chlorophyll/radiation effects , Chromatography, Thin Layer , Culture Media, Serum-Free , Drug Evaluation, Preclinical , Feces/chemistry , Glycoproteins/radiation effects , HIV-1/drug effects , HIV-1/physiology , Hemolysis/drug effects , Herpesvirus 1, Human/drug effects , Herpesvirus 1, Human/physiology , Light , Respirovirus/drug effects , Respirovirus/physiology , Temperature , Virus Replication/drug effects
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