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KLHL22 promotes malignant melanoma growth in vitro and in vivo by activating the PI3K/Akt/mTOR signaling pathway.
Liu, X R; Wang, W; Li, H M.
Afiliação
  • Liu XR; Department of Dermatology, Clinical Center of Spaceport, Chinese PLA General Hospital, Beijing, China.
  • Wang W; Department of Dermatology, No. 929 hospital of the Chinese PLA, Shanghai, China.
  • Li HM; Department of General Practice, Clinical Center of Spaceport, Chinese PLA General Hospital, Beijing, China.
Neoplasma ; 67(5): 1106-1113, 2020 Sep.
Article em En | MEDLINE | ID: mdl-32484697
The kelch like family member 22 (KLHL22) is a member of the KLHL (Kelch-like) gene family, which was involved in the progression of breast cancer. However, its role remains unclear in malignant melanoma (MM). Our study found that KLHL22 expression was upregulated in human MM tissues. Regarding the functional analysis for KLHL22 in the progression of MM cells, we demonstrated that overexpression of KLHL22 could promote MM cell growth in vitro. Vice versa, knockdown of KLHL22 could suppress the proliferation of MM cells. Furthermore, KLHL22 also promoted tumorigenesis of MM cells in vivo. In experiments investigating the underlying mechanism, expressions of p-Akt and p-mTOR were significantly increased by overexpression of KLHL22. Meanwhile, knockdown of KLHL22 could decrease the expression levels of p-Akt and p-mTOR. Our studies thus suggest that KLHL22 can promote the growth of MM cells via activating the PI3K/Akt/mTOR signaling pathway, which can serve as a potential target in the diagnosis and/or treatment of MM.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transdução de Sinais / Proteínas Adaptadoras de Transdução de Sinal / Melanoma Limite: Humans Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transdução de Sinais / Proteínas Adaptadoras de Transdução de Sinal / Melanoma Limite: Humans Idioma: En Ano de publicação: 2020 Tipo de documento: Article