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1.
World J Urol ; 41(6): 1563-1571, 2023 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-37099197

RESUMO

PURPOSE: Few data are available regarding the nephrotoxicity of immune checkpoint inhibitor (ICI) combination therapy in advanced renal cell carcinoma (RCC). This study aimed to investigate the nephrotoxicity of ICI-based combination therapy versus standard of care sunitinib in patients with advanced RCC. METHODS: We searched Embase/PubMed/Cochrane Library for relevant randomized controlled trials (RCTs). Treatment-related nephrotoxicities including increase of creatinine and proteinuria were analyzed by Review Manager 5.4 software. RESULTS: Seven RCTs involving 5239 patients were included. The analysis showed that ICI combination therapy had similar risks of any grade (RR = 1.03, 95% CI: 0.77-1.37, P = 0.87) and grade 3-5 (RR = 1.48, 95% CI: 0.19-11.66, P = 0.71) increased creatinine compared with sunitinib monotherapy. However, ICI combination therapy was associated with significantly higher risks of any grade (RR = 2.33, 95% CI: 1.54-3.51, P < 0.0001) and grade 3-5 proteinuria (RR = 2.25, 95% CI: 1.21-4.17, P = 0.01). CONCLUSIONS: This meta-analysis suggests that ICI combination therapy shows more nephrotoxicity of proteinuria than sunitinib in advanced RCC, which deserves a high attention in the clinic.


Assuntos
Carcinoma de Células Renais , Neoplasias Renais , Humanos , Carcinoma de Células Renais/tratamento farmacológico , Sunitinibe/efeitos adversos , Inibidores de Checkpoint Imunológico/efeitos adversos , Creatinina , Neoplasias Renais/patologia
2.
Inorg Chem ; 60(22): 16906-16910, 2021 Nov 15.
Artigo em Inglês | MEDLINE | ID: mdl-34726390

RESUMO

Herein, a new organic-inorganic hybrid cuprous iodide of [(Me)2-DABCO]Cu6I8 was prepared and structurally characterized with a novel three-dimensional (3D) [Cu6I8]2- framework. Significantly, this 3D cuprous iodide displays infrequent broadband red-to-near-infrared light emission (600-1000 nm) stemming from the radiative recombination of self-trapped excitons.

3.
Chem Commun (Camb) ; 57(56): 6907-6910, 2021 Jul 13.
Artigo em Inglês | MEDLINE | ID: mdl-34151913

RESUMO

Five new zero-dimensional hybrid manganese halides based on discrete [MnCl4]2- tetrahedrons were prepared and used as highly efficient green-light emitters. Through rational management of organic cations to tailor the MnMn separation distances between neighboring [MnCl4]2- tetrahedrons, the photoluminescence quantum yield increased significantly from 7.98% to 81.11%.

4.
Nan Fang Yi Ke Da Xue Xue Bao ; 28(1): 12-5, 2008 Jan.
Artigo em Chinês | MEDLINE | ID: mdl-18227016

RESUMO

OBJECTIVE: To observe the effects of amitrole on the transcription of thyroglobulin (tg), thyroid peroxidase (tpo), Na(+)/I- symporter (nis), Na(+)/I- symporter (nis), thyroid-stimulating hormone receptor (tshr), thyroid transcription factor 1 (ttf-1) and paired-domain protein-8 (pax-8) genes in FRTL-5 cells and investigate the mechanism of amitrole for intervening in thyroid hormone activity. METHODS: FRTL-5 cells were treated with amitrole at 0.001, 0.01 and 0.1 mg/ml for 24 h, respectively, after which the cells were collected for extraction of the total RNA. RT-PCR was used to examine the effects of amitrole on the transcription of tg, tpo, nis, tshr, pax-8 and ttf-1 genes in FRTL-5 cells. RESULTS: Amitrole significantly induced tg gene transcription at all the doses, but produced no obvious effects on tpo and nis gene transcription. At the concentration of 0.1 mg/ml, amitrole significantly reduced pax-8 and tshr gene transcription but increased ttf-1 gene transcription. CONCLUSION: The effects of amitrole on thyroid hormone activity may be related with its actions on tg, ttf-1, tshr and pax-8 gene transcription.


Assuntos
Amitrol (Herbicida)/toxicidade , Proteínas Nucleares/genética , Tireoglobulina/genética , Fatores de Transcrição/genética , Transcrição Gênica/efeitos dos fármacos , Animais , Células Cultivadas , Inibidores Enzimáticos/toxicidade , Células Epiteliais/citologia , Células Epiteliais/efeitos dos fármacos , Células Epiteliais/metabolismo , Ratos , Ratos Endogâmicos F344 , Receptores da Tireotropina/genética , Reação em Cadeia da Polimerase Via Transcriptase Reversa , Glândula Tireoide/citologia , Fator Nuclear 1 de Tireoide
5.
Wei Sheng Yan Jiu ; 34(1): 19-21, 2005 Jan.
Artigo em Chinês | MEDLINE | ID: mdl-15862012

RESUMO

OBJECTIVE: To study the effect of Sulphamethazine on the gene expression of FRTL-5 cells, and to explore the mechaniams of environmental thyroid hormone disruptors. METHODS: cDNA microarray technique was used to analyze the gene expression of FRTL-5 cells of exponential phase treated by 2.0 microg/ml Sulphamethazine for 24 h. Total RNA from treated and untreated cells were labeled by Cy3 dCTP and Cy5 dCTP respectively. The ratios of Cy3/Cy5 were calculated in order to find the genes which expressed differently. RESULTS: There were 679 genes (approximately 7%, total 9753 genes) exhibiting different expression, in which 395 (4.0%) genes up-regulated and 284 (3.0%) genes down-regulated. These genes related to regulation of gene expression, regulation of cell cycle, metabolism in cells, and so on. CONCLUSION: The effect of Sulphamethazine on FRTL-5 cells may be related with a series of genes.


Assuntos
Disruptores Endócrinos/toxicidade , Perfilação da Expressão Gênica , Receptores dos Hormônios Tireóideos/efeitos dos fármacos , Sulfametazina/toxicidade , Glândula Tireoide/efeitos dos fármacos , Animais , Linhagem Celular , Análise de Sequência com Séries de Oligonucleotídeos , Ratos , Receptores dos Hormônios Tireóideos/genética , Glândula Tireoide/citologia , Glândula Tireoide/metabolismo
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