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1.
Leukemia ; 29(12): 2338-46, 2015 Dec.
Article in English | MEDLINE | ID: mdl-26139427

ABSTRACT

We examined the combination of the mammalian target of rapamycin inhibitor everolimus with bortezomib and rituximab in patients with relapsed/refractory Waldenstrom macroglobulinemia (WM) in a phase I/II study. All patients received six cycles of the combination of everolimus/rituximab or everolimus/bortezomib/rituximab followed by maintenance with everolimus until progression. Forty-six patients were treated; 98% received prior rituximab and 57% received prior bortezomib. No dose-limiting toxicities were observed in the phase I. The most common treatment-related toxicities of all grades were fatigue (63%), anemia (54%), leucopenia (52%), neutropenia (48%) and diarrhea (43%). Thirty-six (78%) of the 46 patients received full dose therapy (FDT) of the three drugs. Of these 36, 2 (6%) had complete response (90% confidence interval (CI): 1-16). In all, 32/36 (89%) of patients experienced at least a minimal response (90% CI: 76-96%). The observed partial response or better response rate was 19/36 (53, 90 CI: 38-67%). For the 36 FDT patients, the median progression-free survival was 21 months (95% CI: 12-not estimable). In summary, this study demonstrates that the combination of everolimus, bortezomib and rituximab is well tolerated and achieved 89% response rate even in patients previously treated, making it a possible model of non-chemotherapeutic-based combination therapy in WM.


Subject(s)
Waldenstrom Macroglobulinemia/drug therapy , Aged , Aged, 80 and over , Bortezomib/administration & dosage , Bortezomib/adverse effects , Drug Therapy, Combination , Everolimus/administration & dosage , Everolimus/adverse effects , Female , Humans , Male , Middle Aged , Mutation , Myeloid Differentiation Factor 88/genetics , Receptors, CXCR4/genetics , Recurrence , Rituximab/administration & dosage , Rituximab/adverse effects
2.
Int J Dev Biol ; 45(3): 541-8, 2001.
Article in English | MEDLINE | ID: mdl-11417897

ABSTRACT

Mouse primordial germ cells (PGCs) migrate from the base of the allantois to the genital ridge. They proliferate both during migration and after their arrival, until initiation of the sex-differentiation of fetal gonads. Then, PGCs enter into the prophase of the first meiotic division in the ovary to become oocytes, while those in the testis become mitotically arrested to become prospermatogonia. Growth regulation of mouse PGCs has been studied by culturing them on feeder cells. They show a limited period of proliferation in vitro and go into growth arrest, which is in good correlation with their developmental changes in vivo. However, in the presence of multiple growth signals, PGCs can restart rapid proliferation and transform into pluripotent embryonic germ (EG) cells. Observation of ectopic germ cells and studies of reaggregate cultures suggested that both male and female PGCs show cell-autonomous entry into meiosis and differentiation into oocytes if they were set apart from the male gonadal environments. Recently, we developed a two-dimensional dispersed culture system in which we can examine transition from the mitotic PGCs into the leptotene stage of the first meiotic division. Such entry into meiosis seems to be programmed in PGCs before reaching the genital ridges and unless it is inhibited by putative signals from the testicular somatic cells.


Subject(s)
Germ Cells/cytology , Animals , Apoptosis , Cell Culture Techniques/methods , Cell Differentiation , Female , Growth Substances/physiology , Male , Meiosis , Mice , Oocytes/cytology , Sex Differentiation , Signal Transduction , Spermatozoa/cytology , Stem Cells/cytology
3.
Mech Dev ; 102(1-2): 135-44, 2001 Apr.
Article in English | MEDLINE | ID: mdl-11287187

ABSTRACT

Mammalian sex-determination and differentiation are controlled by several genes, such as Sry, Sox-9, Dax-1 and Mullerian inhibiting substance (MIS), but their upstream and downstream genes are largely unknown. Ad4BP/SF-1, encoding a zinc finger transcription factor, plays important roles in gonadogenesis. Disruption of this gene caused disappearance of the urogenital system including the gonad. Ad4BP/SF-1, however, is also involved in the sex differentiation of the gonad at later stages, such as the regulation of steroid hormones and MIS. Pod-1/Capsulin, a member of basic helix-loop-helix transcription factors, is expressed in a pattern closely related but mostly complimentary to that of the Ad4BP/SF-1 expression in the developing gonad. In the co-transfection experiment using cultured cells, overexpression of Pod-1/Capsulin repressed expression of a reporter gene that carried the upstream regulatory region of the Ad4BP/SF-1 gene. Furthermore, forced expression of Pod-1/Capsulin repressed expression of Ad4BP/SF-1 in the Leydig cell-derived I-10 cells. These results suggest that Pod-1/Capsulin may play important roles in the development and sex differentiation of the mammalian gonad via transcriptional regulation of Ad4BP/SF-1.


Subject(s)
DNA-Binding Proteins/biosynthesis , DNA-Binding Proteins/physiology , Gene Expression Regulation, Developmental , Gonads/metabolism , Transcription Factors/biosynthesis , Transcription Factors/physiology , Animals , Basic Helix-Loop-Helix Transcription Factors , Blotting, Northern , Cell Line , Cells, Cultured , Chloramphenicol O-Acetyltransferase/metabolism , DNA, Complementary/metabolism , Female , Fushi Tarazu Transcription Factors , Genes, Reporter , Homeodomain Proteins , Male , Mice , Mice, Inbred ICR , Plasmids/metabolism , Receptors, Cytoplasmic and Nuclear , Sex Determination Processes , Sex Factors , Steroidogenic Factor 1 , Time Factors , Transfection
4.
Dev Biol ; 229(2): 468-79, 2001 Jan 15.
Article in English | MEDLINE | ID: mdl-11203703

ABSTRACT

Mouse primordial germ cells (PGCs) arrive at the urogenital ridge (UGR) at around 10.5 days postcoitum (dpc). They proliferate until around 13.5 dpc, then enter into meiosis in the female or become mitotically arrested in the male gonads. In this study, meiotic transition of mouse PGCs was examined in vitro. Female PGCs obtained from UGRs or genital ridges at 10.5-11.5 dpc began to express meiosis-specific genes, Scp3 and Dmc1, after dissociation and cultivation on feeder cells for several days. Meiotic transition into the leptotene stage was confirmed by the formation of axial cores. Male PGCs at 10.5-11.5 dpc and migratory PGCs obtained from mesenteries at 10.5 dpc also expressed Scp3 and formed axial cores after several days of culture, supporting the hypothesis that PGCs are capable of entering meiosis before arriving at the UGR. gp130-mediated signaling, known to promote survival/growth of PGCs and also to inhibit the differentiation of embryonic stem cells, suppressed the expression of Scp3 in PGCs and inhibited the following formation of axial cores in vitro. This novel activity of gp130-mediated signaling may provide some clues for the understanding of pluripotency of mammalian germ-line cells and/or the sex differentiation of fetal germ cells.


Subject(s)
Adenosine Triphosphatases , Cell Cycle Proteins , Ovum/cytology , Spermatozoa/cytology , Animals , DNA-Binding Proteins/genetics , Embryonic and Fetal Development , Female , Gene Expression Regulation, Developmental , Genotype , Ligases/genetics , Male , Meiosis , Mice , Mice, Inbred ICR , Nuclear Proteins/genetics , Phosphate-Binding Proteins , Reverse Transcriptase Polymerase Chain Reaction , Sex Determination Analysis , Synaptonemal Complex/genetics , Ubiquitin-Protein Ligases
5.
FEBS Lett ; 487(2): 248-51, 2000 Dec 29.
Article in English | MEDLINE | ID: mdl-11150518

ABSTRACT

We aimed to introduce foreign DNA into spermatogenic cells in the testis by injection of the DNA encoding jellyfish fluorescent proteins, green fluorescent protein (GFP) and yellow fluorescent protein (YFP) into the seminiferous tubules and in vivo electroporation. We obtained fluorescent spermatozoa only when using the gene of the YFP protein fused to a mitochondrial localization signal peptide. Intracytoplasmic injection into oocytes of these spermatozoa gave fluorescent fetuses and pups. Almost all of the individuals produced from fluorescent spermatozoa were transgenic. We confirmed integration of the gene into chromosomes and its transmission into offspring. This is the first report of gene transfer into germ cells and subsequent production of transgenic offspring.


Subject(s)
Luminescent Proteins/genetics , Mitochondria/physiology , Seminiferous Tubules/physiology , Spermatozoa/physiology , Animals , Bacterial Proteins/analysis , Bacterial Proteins/genetics , Electroporation , Gene Transfer Techniques , Genes, Reporter , Green Fluorescent Proteins , Luminescent Proteins/analysis , Male , Mice , Mice, Inbred C57BL , Mice, Inbred DBA , Mice, Inbred ICR , Mitochondria/ultrastructure , Protein Sorting Signals , Scyphozoa , Sperm Injections, Intracytoplasmic
6.
Int J Dev Biol ; 43(8): 777-84, 1999 Nov.
Article in English | MEDLINE | ID: mdl-10707901

ABSTRACT

Sex-differentiation in mammals initiates at mid-gestation when the differentiation of Sertoli cells is triggered by the expression of the testis-determining gene, Sry. However, little is known about the succeeding germ-soma interaction that directs the sex-differentiation of germ cells. We carried out subtraction and differential screening between male and female gonads at 13.5 dpc (days post coitum). A novel cystatin-related gene was identified and named cresp (cystatin-related expressed in Sertoli and spermatogonia), and has recently been reported independently under the name testatin (Töhönen et al., 1998). The presumed amino acid sequence of testatin/cresp showed considerable homology to the cystatin family, but it lacked a few critical amino acid residues for the cysteine-protease inhibitory activity. A 0.7 kb RNA was detected by northern blotting specifically in the fetal and adult testes from 11.5 dpc and expression increased between 11.5 dpc and 12.5 dpc. Using RT-PCR analysis, the testatin/cresp mRNA was first detectable at 9.5 dpc in both male and female embryos but it was maintained only in the male. In females, the expression became weaker at 11.5 dpc and was undetectable after 12.0 dpc. In situ hybridization and immunohistochemical analyses, as well as single cell RT-PCR analysis, showed that the testatin/cresp mRNA was localized specifically in both the (pro)spermatogonia and Sertoli cells in the testis from 12.5 dpc to adult. Thus, expression of the testatin/cresp gene is upregulated in male gonads but downregulated in females immediately after the initiation of sex-differentiation, suggesting roles in the early developmental cascade of testis such as the germ-soma interaction.


Subject(s)
Cystatins/genetics , Sex Differentiation/genetics , Amino Acid Sequence , Animals , Base Sequence , Cloning, Molecular , DNA Primers/genetics , DNA, Complementary/genetics , Female , Gene Expression Regulation, Developmental , In Situ Hybridization , Male , Mice , Molecular Sequence Data , RNA, Messenger/genetics , RNA, Messenger/metabolism , Reverse Transcriptase Polymerase Chain Reaction , Sequence Homology, Amino Acid , Sertoli Cells/cytology , Sertoli Cells/metabolism , Spermatogonia/cytology , Spermatogonia/metabolism , Testis/cytology , Testis/embryology , Testis/metabolism
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