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Prognostic Impact and Immunotherapeutic Implications of NETosis-related Prognostic Model in Clear Cell Renal Cell Carcinoma

Overview
Specialty Oncology
Date 2024 May 27
PMID 38801430
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Abstract

Background: The ramifications of necroptosis on the prognostication of clear cell renal cell carcinoma (ccRCC) remain inadequately expounded.

Methods: A prognostic model delineating the facets of necroptosis in ccRCC was constructed, employing a compendium of algorithms. External validation was effectuated using the E-MTAB-1980 dataset. The exploration of immune infiltration scores was undertaken through the exploitation of multiple algorithms. Single-cell RNA sequencing data were procured from the GSE171306 dataset. Real-time quantitative PCR (RT-qPCR) was engaged to scrutinize the differential expression of SLC25A37 across cancer and paracancer tissues, as well as diverse cell lines. Assessments of proliferative and metastatic alterations in 769-P and 786-O cells were accomplished through Cell Counting Kit-8 (CCK8) and wound healing assays.

Results: The necroptosis-related signature (NRS) emerges as a discerning metric, delineating patients' immune attributes, tumor mutation burden, immunotherapy response, and drug susceptibility. Single-cell RNA sequencing analysis unveils the marked enrichment of SLC25A37 in tumor cells. Concurrently, RT-qPCR discloses the overexpression of SLC25A37 in both ccRCC tissues and cell lines. SLC25A37 knockdown mitigates the proliferative and metastatic propensities of 769-P and 786-O cells, as evidenced by CCK8 and wound healing assays.

Conclusion: The NRS assumes a pivotal role in ascertaining the prognosis, tumor mutation burden, immunotherapy response, drug susceptibility, and immune cell infiltration features of ccRCC patients. SLC25A37 emerges as a putative player in immunosuppressive microenvironments, thereby providing a prospective avenue for the design of innovative immunotherapeutic targets for ccRCC.

References
1.
De Marco S, Torsello B, Minutiello E, Morabito I, Grasselli C, Bombelli S . The cross-talk between Abl2 tyrosine kinase and TGFβ1 signalling modulates the invasion of clear cell Renal Cell Carcinoma cells. FEBS Lett. 2022; 597(8):1098-1113. DOI: 10.1002/1873-3468.14531. View

2.
Yin Y, Dai H, Sun X, Xi Z, Zhang J, Pan Y . HRG inhibits liver cancer lung metastasis by suppressing neutrophil extracellular trap formation. Clin Transl Med. 2023; 13(6):e1283. PMC: 10230156. DOI: 10.1002/ctm2.1283. View

3.
Han Y, Wang Y, Dong X, Sun D, Liu Z, Yue J . TISCH2: expanded datasets and new tools for single-cell transcriptome analyses of the tumor microenvironment. Nucleic Acids Res. 2022; 51(D1):D1425-D1431. PMC: 9825603. DOI: 10.1093/nar/gkac959. View

4.
Weide L, Schedel F, Weishaupt C . Neutrophil Extracellular Traps Correlate with Tumor Necrosis and Size in Human Malignant Melanoma Metastases. Biology (Basel). 2023; 12(6). PMC: 10295294. DOI: 10.3390/biology12060822. View

5.
Guillotin F, Fortier M, Portes M, Demattei C, Mousty E, Nouvellon E . Vital NETosis vs. suicidal NETosis during normal pregnancy and preeclampsia. Front Cell Dev Biol. 2023; 10:1099038. PMC: 9849884. DOI: 10.3389/fcell.2022.1099038. View