Objective <p>In this study, we preliminarily investigated the efffects of the colony stimulating factor 1 receptor (CSF1R) molecules on CD8<sup>+</sup> T cells in bladder cancer (BLCA) and the underlying molecular mechanism.</p> Methods <p>The effects of CSF1R in CD8<sup>+</sup> T cells on BLCA cell proliferation, migration and, invasion were determined by cell-killing assay and transwell assays.For in vivo experiments, tumours tissues were divided into four portions: (1) histological staining, (2) flow cytometry detection, (3) mRNA gene sequencing analysis, and (4) qPCR validation. Information related to 161 bladder cancer patients with BLCA at Xiangya Hospital of Central South University from 2019 to 2023 was collected. The pathological tissues were subjected to immunofluorescence. By calculating the Jordon index, CD8<sup>+</sup> T cells with CSF1R expression at or above 0.39-fold were included in the high-expression group.</p> Results <p>Knocking down of CSF1R in CD8<sup>+</sup> T cells inhibited BLCA proliferation, migration, and invasion. Flow cytometry revealed that it could lead to increased infiltration of immune cells. mRNA sequencing, quantitative polymerase chain reaction (PCR) and Western blot (WB) results suggested that creatine kinase (Ckm) was significantly decreased after CSF1R knockdown.</p> Conclusion <p>Our study provides novel insights into the roles of CSF1R in BLCA progression and the underlying crosstalk between tumour metabolism and the immune microenvironment.</p>

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Knockdown of CSF1R molecules enhances the antitumor effects of CD8+ T lymphocytes in bladder cancer

  • Jingxuan Peng,
  • Dongjie Li,
  • Boyu Xiang,
  • Zhongyi Li,
  • Zhengyan Tang

摘要

Objective

In this study, we preliminarily investigated the efffects of the colony stimulating factor 1 receptor (CSF1R) molecules on CD8+ T cells in bladder cancer (BLCA) and the underlying molecular mechanism.

Methods

The effects of CSF1R in CD8+ T cells on BLCA cell proliferation, migration and, invasion were determined by cell-killing assay and transwell assays.For in vivo experiments, tumours tissues were divided into four portions: (1) histological staining, (2) flow cytometry detection, (3) mRNA gene sequencing analysis, and (4) qPCR validation. Information related to 161 bladder cancer patients with BLCA at Xiangya Hospital of Central South University from 2019 to 2023 was collected. The pathological tissues were subjected to immunofluorescence. By calculating the Jordon index, CD8+ T cells with CSF1R expression at or above 0.39-fold were included in the high-expression group.

Results

Knocking down of CSF1R in CD8+ T cells inhibited BLCA proliferation, migration, and invasion. Flow cytometry revealed that it could lead to increased infiltration of immune cells. mRNA sequencing, quantitative polymerase chain reaction (PCR) and Western blot (WB) results suggested that creatine kinase (Ckm) was significantly decreased after CSF1R knockdown.

Conclusion

Our study provides novel insights into the roles of CSF1R in BLCA progression and the underlying crosstalk between tumour metabolism and the immune microenvironment.