Prognostic Model Associated with Necroptosis in Colorectal Cancer based on Transcriptomic Analysis and Experimental Validation

Numerous studies have emphasised the importance of necroptosis in the malignant progression of colorectal cancer (CRC). However, whether necroptosis-related genes (NRGs) can be used to predict the prognosis of CRC remains to be revealed. Patients with CRC were divided into two clusters based on the...

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Veröffentlicht in:Frontiers in bioscience (Landmark. Print) 2024-03, Vol.29 (3), p.98-98
Hauptverfasser: Huang, Yuying, Li, Licheng, Kang, Zhongmin, Luo, Huali, Lin, Xiaojing, Zhao, Shu, Zhang, Qizhu, Li, Qinshan, Liu, Honglin, Li, Mengxing
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Sprache:eng
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Zusammenfassung:Numerous studies have emphasised the importance of necroptosis in the malignant progression of colorectal cancer (CRC). However, whether necroptosis-related genes (NRGs) can be used to predict the prognosis of CRC remains to be revealed. Patients with CRC were divided into two clusters based on the expression of NRGs, and prognosis was compared between the two clusters. A prognostic model was established based on NRGs, and its predictive efficiency was validated using Kaplan-Meier (K-M) curves, receiver operating characteristic (ROC) curves and a nomogram. Immune infiltration, single-cell and drug sensitivity analyses were used to examine the effects of NRGs on the prognosis of CRC. The prognostic model served as a valid and independent predictor of CRC prognosis. Immune infiltration and single-cell analyses revealed that the unique immune microenvironment of CRC was regulated by NRGs. Drug sensitivity analysis showed that patients in the high- and low-risk groups were sensitive to different drugs. In addition, was found to play an important role in regulating the malignant progression of CRC. This study provides novel insights into precision immunotherapy based on NRGs in CRC. The NRG-based prognostic model may help to identify targeted drugs and develop more effective and individualised treatment strategies for patients with CRC.
ISSN:2768-6701
2768-6698
DOI:10.31083/j.fbl2903098