4.7 Article

The immune-related biomarker TEK inhibits the development of clear cell renal cell carcinoma (ccRCC) by regulating AKT phosphorylation

Journal

CANCER CELL INTERNATIONAL
Volume 21, Issue 1, Pages -

Publisher

BMC
DOI: 10.1186/s12935-021-01830-1

Keywords

Clear cell renal cell carcinoma; Tumor microenvironment; Survival prognosis; Tumor-infiltrating immune cells; TEK

Categories

Funding

  1. National Natural Science Foundation of China [31900902]
  2. Health commission of Hubei Province scientific research project [WJ2019H023]
  3. Fundamental Research Funds for the Central Universities [2042019kf0150]

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The study identified TEK as a crucial immune marker highly related to survival prognosis in ccRCC. Knockdown of TEK was found to promote cell proliferation and migration, while promoting apoptosis by regulating AKT phosphorylation. This suggests that TEK may be an emerging target for immunotherapy in ccRCC patients.
BackgroundHigh immunogenicity is an important feature of ccRCC, but its underlying immune-related molecular mechanisms remain unclear. This study aimed to investigate the effect of immune-related gene TEK on ccRCC and its prognostic value.MethodsThe immune-related differentially expressed genes (DEGs) and transcription factors (TFs) in ccRCC were screened based on The Cancer Genome Atlas (TCGA) database, and a regulatory network of TF was constructed. Prognostic-related immune genes were screened by univariate Cox regression analysis and functional annotation was performed. Univariate and multivariate Cox regression analyses were performed to construct the immune gene risk model and identify the hub gene TEK that independently affected the prognosis of ccRCC. The effectiveness of the TEK was verified by external microarray datasets. The relationship between TEK and immune cells in ccRCC was evaluated based on Tumor Immune Estimation Resource (TIMER). The expression of TEK in clinical specimens was verified by qRT-PCR and immunohistochemical (IHC) staining. MTT and cloning formation assay were used to evaluate cell proliferation. Transwell assays were used to assess cell migration. Apoptosis was assessed by flow cytometry, and the expression of related proteins was detected by Western blot and immunofluorescence.ResultsWe constructed a prognostic model consisting of 12 hub genes and performed risk scores to determine the relationship between these scores and prognosis. Through Cox regression analysis and survival analysis, TEK, an immune marker highly related to survival prognosis, was obtained and validated. In vitro experiments showed that knockdown of TEK promoted the proliferation and migration of ccRCC cells, and we found that TEK promoted apoptosis by regulating the phosphorylation of AKT, thereby inhibiting cell proliferation.ConclusionsTEK plays an important role in risk assessment and survival prediction for ccRCC patients as a new immune gene and maybe an emerging target for immunotherapy for ccRCC patients.

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