Abstract
Background
Limited evidence suggests that nucleolar protein interacting with the FHA domain of MKI67 (NIFK) plays a significant role in tumour occurrence and development. The mechanism and clinical value of NIFK in colorectal cancer (CRC) still lack a comprehensive evaluation.
Materials and Methods
Cancerous tissue and paracancerous tissue of 266 CRC patients were collected for immunohistochemistry, and the mRNA expression profiles of 2262 CRC tissue and 1297 non-CRC tissue worldwide were collected and analysed at the NIFK protein and mRNA levels. Analyse the effect of knocking out NIFK by CRISPR on the growth status of CRC cells in 43 CRC cell lines. Enrichment analysis was used to explore the potential biological behaviour of NIFK in the CRC. The impact of NIFK on the immune microenvironment and single-cell landscape of CRC tissue was also analysed. In addition, the clinical value of NIFK in CRC was also evaluated in terms of clinical pathology, targeted therapy, and immunotherapy.
Results
The expression levels of NIFK protein (p < 0.05) and mRNA (SMD = 2.13, p < 0.05) in CRC were significantly higher than those in non-CRC. CRC cells exhibit a strong requirement for NIFK for growth. Abnormal expression of NIFK may affect the progression of CRC by affecting the GALECTIN, ANGPTL, and GDF signalling pathways of malignant epithelial cells, the MIF signalling pathway of T cells, and the TGFb signalling pathway of NK cells. The high expression of NIFK protein and mRNA has a strong ability to identify CRC.
Conclusion
NIFK plays an important role in the occurrence and development of CRC. NIFK may promote the occurrence and development of CRC through the cell cycle, ribosome, and mitochondrial pathways. The T-cell MIF pathway may have certain clinical value in anti-tumour therapy.