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Decreased TSPAN14 Expression Contributes to NSCLC Progression.
Jovanovic, Mirna; Stankovic, Tijana; Stojkovic Buric, Sonja; Bankovic, Jasna; Dinic, Jelena; Ljujic, Mila; Pesic, Milica; Dragoj, Miodrag.
Afiliação
  • Jovanovic M; Department of Neurobiology, Institute for Biological Research "Sinisa Stankovic"-National Institute of the Republic of Serbia, University of Belgrade, Despota Stefana 142, 11060 Belgrade, Serbia.
  • Stankovic T; Department of Neurobiology, Institute for Biological Research "Sinisa Stankovic"-National Institute of the Republic of Serbia, University of Belgrade, Despota Stefana 142, 11060 Belgrade, Serbia.
  • Stojkovic Buric S; Department of Neurobiology, Institute for Biological Research "Sinisa Stankovic"-National Institute of the Republic of Serbia, University of Belgrade, Despota Stefana 142, 11060 Belgrade, Serbia.
  • Bankovic J; Department of Neurobiology, Institute for Biological Research "Sinisa Stankovic"-National Institute of the Republic of Serbia, University of Belgrade, Despota Stefana 142, 11060 Belgrade, Serbia.
  • Dinic J; Department of Neurobiology, Institute for Biological Research "Sinisa Stankovic"-National Institute of the Republic of Serbia, University of Belgrade, Despota Stefana 142, 11060 Belgrade, Serbia.
  • Ljujic M; Institute of Molecular Genetics and Genetic Engineering, University of Belgrade, Vojvode Stepe 444a, 11042 Belgrade, Serbia.
  • Pesic M; Department of Neurobiology, Institute for Biological Research "Sinisa Stankovic"-National Institute of the Republic of Serbia, University of Belgrade, Despota Stefana 142, 11060 Belgrade, Serbia.
  • Dragoj M; Department of Neurobiology, Institute for Biological Research "Sinisa Stankovic"-National Institute of the Republic of Serbia, University of Belgrade, Despota Stefana 142, 11060 Belgrade, Serbia.
Life (Basel) ; 12(9)2022 Aug 23.
Article em En | MEDLINE | ID: mdl-36143328
Tspan14 is a transmembrane protein of the tetraspanin (Tspan) protein family. Different members of the Tspan family can promote or suppress tumor progression. The exact role of Tspan14 in tumor cells is unknown. Earlier, mutational inactivation of the TSPAN14 gene has been proposed to coincide with a low survival rate in NSCLC patients. This study aimed to investigate the correlation of TSPAN14 lack of function with clinicopathological features of NSCLC patients, and to elucidate the role TSPAN14 might have in NSCLC progression. TSPAN14 expression was lower in tumor cells than non-tumor cells in NSCLC patients' samples. The decreased gene expression was correlated with a low survival rate of patients and was more frequent in patients with aggressive, invasive tumor types. Additionally, the role of decreased TSPAN14 expression in the metastatic potential of cancer cells was confirmed in NSCLC cell lines. The highly invasive NSCLC cell line (NCI-H661) had the lowest TSPAN14 gene and protein expression, whereas the NSCLC cell line with the highest TSPAN14 expression (NCI-H460) had no significant metastatic potential. Finally, silencing of TSPAN14 in these non-metastatic cancer cells caused an increased expression of matrix-degrading enzymes MMP-2 and MMP-9, followed by an elevated capacity of cancer cells to degrade gelatin. The results of this study propose TSPAN14 expression as an indicator of NSCLC metastatic potential and progression.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Life (Basel) Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Life (Basel) Ano de publicação: 2022 Tipo de documento: Article