Your browser doesn't support javascript.
loading
Gelsolin knockdown confers radiosensitivity to glioblastoma cells.
Gao, Dezhi; Jiang, Tao; Liu, Yanwei.
Afiliación
  • Gao D; Beijing Neurosurgical Institute, Capital Medical University, Beijing, China.
  • Jiang T; Department of Gamma-Knife Center, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.
  • Liu Y; Beijing Neurosurgical Institute, Capital Medical University, Beijing, China.
Cancer Med ; 13(10): e7286, 2024 May.
Article en En | MEDLINE | ID: mdl-38803199
ABSTRACT

OBJECTIVE:

Radiotherapy (RT) is a cornerstone of the glioblastoma (GBM) treatment. However, the resistance of tumour cells to radiation results in early recurrence. The mechanisms underlying GBM radioresistance remain unclear. Screening for differentially expressed genes (DEGs) related to radiation might be a potential solution to this problem.

METHOD:

RT-associated DEGs were screened based on the RNA sequencing of 15 paired primary and recurrent GBMs. The mRNA and protein expression of candidate genes were validated in RNA sequencing of The Chinese Genome Atlas (CGGA) dataset and 18 cases of GBM samples. The relationship between the candidate gene and radiation was confirmed in irradiated GBM cells. The association of candidate gene with clinical characteristics and survival was investigated in the CGGA and TCGA dataset. Biological function and pathway analysis were explored by gene ontology analysis. The association of the candidate gene with radiosensitivity was verified using cell counting Kit-8, comet, and colony formation assays in vitro and subcutaneous tumour xenograft experiments in vivo.

RESULTS:

Gelsolin (GSN) was selected for further study. GSN expression was significant elevated in recurrent GBM and up-regulated in irradiated GBM cell lines. High expression of GSN was enriched in malignant phenotype of glioma. Moreover, high expression of GSN was associated with poor prognosis. Further investigation demonstrated that GSN-knockdown (GSN-KD) combined with RT significantly inhibited cell proliferation and enhanced radiosensitivity in vivo and in vitro. Mechanistically, GSN-KD could lead to more serious DNA damage and promotes apoptosis after RT.

CONCLUSION:

Radiation induced up-regulated of GSN. GSN-KD could enhance the radiosensitivity of GBM.
Asunto(s)
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Tolerancia a Radiación / Neoplasias Encefálicas / Regulación Neoplásica de la Expresión Génica / Gelsolina / Glioblastoma Límite: Animals / Female / Humans / Male Idioma: En Revista: Cancer Med Año: 2024 Tipo del documento: Article País de afiliación: China Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Tolerancia a Radiación / Neoplasias Encefálicas / Regulación Neoplásica de la Expresión Génica / Gelsolina / Glioblastoma Límite: Animals / Female / Humans / Male Idioma: En Revista: Cancer Med Año: 2024 Tipo del documento: Article País de afiliación: China Pais de publicación: Estados Unidos