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1.
Chinese Journal of Oncology ; (12): 84-90, 2011.
Artigo em Chinês | WPRIM | ID: wpr-303361

RESUMO

<p><b>OBJECTIVE</b>To isolate and characterize the side population cells (SP cells) in the lung adenocarcinomas cell line A549.</p><p><b>METHODS</b>The protein expression of ABCG2 in human lung adenocarcinoma cell line A549 was detected by immunohistochemistry. SP and NSP cells in the cell line A549 were isolated by FACS, and their differentiation was analysed. ABCG2 expression in the two cell subsets was detected by RT-PCR. The cell growth curves, cell division indexes, cell cycles, plate clone formation tests, migration and invasion assays, chemotherapeutic susceptibility tests, tests of the intracellular drug levels, and the tumor cell implantation experiments on nude mice were applied to study the biological properties of the two cell subsets. The expression of ABCG2 in the transplanted tumor in nude mice was detected by immunohistochemistry and RT-PCR.</p><p><b>RESULTS</b>The positive rate of ABCG2 expression in the A549 cells by immunohistochemistry was 2.13%. SP and NSP cells were isolated by FACS. The SP cells could produce both SP and NSP cells, while NSP cells only produced NSP cells. SP cells expressed ABCG2, but NSP cells did not. The proliferation and migration abilities of the two cell subsets were similar, but the invasion and tumorigenic ability of SP cells was significantly higher than that of NSP cells. The susceptibilities to DDP and its intracellular levels of the two cell subsets were similar, but the susceptibilities to 5-FU, VP16, NVB and GEM and their intracellular levels of NSP cells were significantly higher than those of the SP cells.</p><p><b>CONCLUSIONS</b>SP cells in the human lung adenocarcinomas cell line A549 is enriched with tumor stem cells. An effective way to get lung adenocarcinomas stem cells is to isolate SP cells by FACS.</p>


Assuntos
Animais , Humanos , Transportadores de Cassetes de Ligação de ATP , Metabolismo , Adenocarcinoma , Patologia , Ciclo Celular , Diferenciação Celular , Linhagem Celular Tumoral , Proliferação de Células , Transformação Celular Neoplásica , Metabolismo , Fluoruracila , Metabolismo , Neoplasias Pulmonares , Patologia , Camundongos Nus , Proteínas de Neoplasias , Metabolismo , Transplante de Neoplasias , Células-Tronco Neoplásicas , Células da Side Population
2.
Chinese Journal of Oncology ; (12): 528-531, 2008.
Artigo em Chinês | WPRIM | ID: wpr-357382

RESUMO

<p><b>OBJECTIVE</b>To evaluate the relationship between combined multigene detection and response to adjuvant chemotherapy and prognosis in early-stage non-small cell lung cancer (NSCLC).</p><p><b>METHODS</b>Tissue microarray was prepared from samples of 86 cases of early-stage NSCLC who received adjuvant chemotherapy after radical surgery. The expressions of caspase-3, Fas, bax, bcl-2, survivin, PCNA, Ki67, MGMT, p53, p63, p73, p16, p27, VEGF, nm23, P-gp, MRP, LRP, GST-pi, Topo II, c-myc, cyclin-D1, Her-2, Cox-2, Ku70, Ku80, DNA-PKcs, ERCC1, MSH2, BCRP proteins were detected using immunohistochemical two-step method.</p><p><b>RESULTS</b>The positive rate of the 30 genes in lung cancer tissue were 27.9% - 91.9%, respectively. By univariate analysis, the expression of 8 genes was shown to be related with SCLC adjuvant chemotherapy. The cases with higher expression of survivin, P-gp, LRP, Ki67, p53, ERCC1 and lower expression of bax,VEGF had worse prognosis. By logistic regression analysis, the ERCC1, survivin, bax and VEGF were a marker group. Multivariate analysis showed the predict value of the response to adjuvant chemotherapy in early-stage NSCLC was 96.5%.</p><p><b>CONCLUSION</b>Survivin, ERCC1, bax and VEGF are an ideal marker group to predict the effect of adjuvant chemotherapy in early-stage NSCLC.</p>


Assuntos
Adulto , Idoso , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Carcinoma Pulmonar de Células não Pequenas , Tratamento Farmacológico , Metabolismo , Patologia , Cirurgia Geral , Quimioterapia Adjuvante , Proteínas de Ligação a DNA , Metabolismo , Endonucleases , Metabolismo , Seguimentos , Proteínas Inibidoras de Apoptose , Modelos Logísticos , Neoplasias Pulmonares , Tratamento Farmacológico , Metabolismo , Patologia , Cirurgia Geral , Proteínas Associadas aos Microtúbulos , Metabolismo , Estadiamento de Neoplasias , Taxa de Sobrevida , Análise Serial de Tecidos , Fator A de Crescimento do Endotélio Vascular , Metabolismo , Proteína X Associada a bcl-2 , Metabolismo
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