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1.
Chinese Journal of Applied Clinical Pediatrics ; (24): 1643-1646, 2013.
Article in Chinese | WPRIM | ID: wpr-733198

ABSTRACT

Objective To identify and analyze a novel transcript 630 in acute T-cell lymphoblastic leukemia cell (T-ALL) Jurkat cell lines.Methods RNA-sequencing was applied to transcriptome profiling.The novel transcript 630 was identified by reverse transcription polymerase chain reaction (RT-PCR) combined with sequencing.The expression level of the novel transcript was detected in some tumor cell lines and normal cells.The sequences for small interfering RNA (siRNA) against 630 were designed and synthesized.Then,the effects of siRNA were determined by real-time PCR.Apoptotic cells and cell cycle analysis were investigated with the flow cytometry after siRNA-mediated knockdown of 630.Results The novel transcript 630 was identified.High expression level of 630 was detected in Jurkat E6-1,HL60 and human umbilical vein endothelial(HUVE) cells.The knockdown of transcript 630 induced a decrease of cellular proliferation.Conclusions The novel transcript 630 is one of the novel transcripts in Jurkat cells.The decreased expression level of transcript 630 can suppress the proliferation of leukemia cells.The novel transcript 630 might contribute to the treatment of T-ALL.

2.
Chinese Journal of Applied Clinical Pediatrics ; (24): 183-187, 2013.
Article in Chinese | WPRIM | ID: wpr-732939

ABSTRACT

Objective To establish an acute graft-versus-host disease (aGVHD) model in EL4 T-cell leukemia/lymphoma mice,for providing experimental model to prevent aGVHD while maintaining graft-versus-leu1 mia (GVL) effect during allogeneic bone marrow transplantation (Allo-BMT).Methods Male BALB/c (H-2Kd)mice were used as donors and female C57BL/6(H-2Kb) mice were used as recipients.C57BL/6 hosts were given 9.5 Gy lethal total body irradiation at 4 hours prior to transplantation.Mice were randomly assigned into 3 groups and each group contained 17 recipients:The recipients in radiation group were injected with 0.2 mL RPMI 1640 as control.The recipients were injected with donor bone marrow cells (5 × 106/mouse) and splenocyte for aGVHD(5 × 106/mouse).The recipients in EL4 T-cell leukemia/lymphoma aGVHD group were injected with donor bone marrow cells (5 × 106/mouse) and plus 500 EL4 cells (5 × 106/mouse).General state,life span and histopathology of the recipient mice and detected chimera were observed.Results The results showed that the mean survival time in radiation group was (10.10 ± 0.43) days,in aGVHD group was(28.12 ± 5.01)days,in EL4 T-cell leukemia/lymphoma aGVHD group was (31.05 ±5.48) days.The mean survival time in aGVHD group and EL4 T-cell leukemia/lymphoma aGVHD group were significantly longer than that in radiation group(all P < 0.01),but there was no significant difference between aGVHD group and EL4 T-cell leukemia/lymphoma aGVHD group (P > 0.05).Histopathological analysis in several target organs (skin,liver and small intestine) confirmed the presence of sever GVHD in aGVHD group and EL4 T-cell leukemia/ lymphoma aGVHD group.Pathological examination showed disorganization of normal tissues and leukemic cell infiltration in EL4 T-cell leukemia/lymphoma aGVHD group.Conclusion The EL4 T-cell leukemia/lymphoma aGVHD mice model is reliable to the experimental research of aGVHD.

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