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1.
Int J Mol Med ; 46(6): 2007-2018, 2020 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-33125097

RESUMO

Long intergenic non­coding RNA 01232 (LINC01232) was identified as a critical regulator of the development of pancreatic adenocarcinoma. The present study investigated the expression and regulatory roles of LINC01232 in esophageal squamous cell carcinoma (ESCC). The main aim of the present study was to elucidate the underlying mechanisms through which LINC01232 affects the malignancy of ESCC. Initially, LINC01232 expression in ESCC was analyzed using the TCGA and GTEx databases and was confirmed using reverse transcription­quantitative polymerase chain reaction. ESCC cell proliferation, apoptosis and migration and invasion were assessed using the Cell Counting kit­8 assay, flow cytometric analysis, and migration and invasion assays, respectively. ESCC tumor growth in vivo was examined using a xenograft mouse model. As shown by the results, a high LINC01232 expression was detected in ESCC tissues and cell lines. LINC01232 downregulation suppressed the proliferation, migration and invasion of ESCC cells, and promoted cell apoptosis in vitro. In addition, LINC01232 depletion restricted tumor growth in vivo. Mechanistically, LINC01232 was shown to function as an microRNA­654­3p (miR­654­3p) sponge in ESCC cells, and hepatoma­derived growth factor (HDGF) was identified as a direct target of miR­654­3p. LINC01232 could bind competitively to miR­654­3p and decrease its expression in ESCC cells, thereby promoting HDGF expression. Rescue experiments reconfirmed that the effects of LINC01232 deficiency in ESCC cells were restored by increasing the output of the miR­654­3p/HDGF axis. On the whole, the present study demonstrates that LINC01232 plays a tumor­promoting role during the progression of ESCC by regulating the miR­654­3p/HDGF axis. The LINC01232/miR­654­3p/HDGF pathway may thus provide a novel theoretical basis for the management of ESCC.


Assuntos
Progressão da Doença , Neoplasias Esofágicas/genética , Carcinoma de Células Escamosas do Esôfago/genética , Carcinoma de Células Escamosas do Esôfago/patologia , Regulação Neoplásica da Expressão Gênica , Peptídeos e Proteínas de Sinalização Intercelular/genética , MicroRNAs/metabolismo , RNA Longo não Codificante/genética , Idoso , Animais , Sequência de Bases , Linhagem Celular Tumoral , Proliferação de Células/genética , Neoplasias Esofágicas/patologia , Feminino , Técnicas de Silenciamento de Genes , Humanos , Peptídeos e Proteínas de Sinalização Intercelular/metabolismo , Masculino , Camundongos Endogâmicos BALB C , Camundongos Nus , MicroRNAs/genética , Pessoa de Meia-Idade , RNA Longo não Codificante/metabolismo , Regulação para Cima/genética
2.
Zhonghua Yi Shi Za Zhi ; 34(3): 162-5, 2004 Jul.
Artigo em Chinês | MEDLINE | ID: mdl-15555228

Assuntos
Médicos , Humanos
3.
Zhong Yao Cai ; 26(2): 119-20, 2003 Feb.
Artigo em Chinês | MEDLINE | ID: mdl-12795226

RESUMO

By herbalogical study and investigation, "Zhanba" used by Mongolia doctors mainly contains 7 species from 3 genera of 1 family, but "Zhanba" in Inner Mongolia Standard of Medicinal Materials only contains 3 species which are Althaea rosea, Malva sylvestris L. var. mauritiana and M. verticillata.


Assuntos
Althaea/anatomia & histologia , Medicamentos de Ervas Chinesas/história , Malva/anatomia & histologia , Farmacognosia/história , Plantas Medicinais/anatomia & histologia , China , Contaminação de Medicamentos/prevenção & controle , História do Século XVIII , História do Século XIX , História Antiga , História Medieval , Mongólia
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