Serum tRF5-23-GlyTCC-2 Functions as a Tumor Suppressor and Novel Biomarker for Colorectal Cancer

Xinhui Lv,1,2 Hui Dai,1,2 Yu Wu,1,2 Jiyuan Yang,1,2 Guihua Wang,1,2 Xudong Wang1,2 1Department of Laboratory Medicine, Affiliated Hospital of Nantong University, Nantong, Jiangsu, People’s Republic of China; 2Medical School of Nantong University, Nantong, Jiangsu, People’s Republic of ChinaCorrespondence: Xudong Wang, Department of Laboratory Medicine, Affiliated Hospital of Nantong University, Medical School of Nantong University, Nantong, Jiangsu, 226001, People’s Republic of China, Tel +86-13951318000, Email [email protected]: Transfer RNA-derived small RNAs (tsRNAs) are a recently discovered class of non-coding RNAs with aberrant expression in various cancers. Substantial evidence implicates tsRNAs in the initiation and progression of colorectal cancer (CRC). This study aimed to investigate the diagnostic and prognostic potential of a specific tsRNA, tRF5-23-GlyTCC-2, in CRC.Methods: We identified tRF5-23-GlyTCC-2 via high-throughput RNA sequencing and validated its expression using qRT-PCR. Associations between tRF5-23-GlyTCC-2 expression, clinicopathological features, and patient survival were assessed with Chi-square and Kaplan-Meier analyses. Its diagnostic performance was evaluated by ROC curve analysis. Functional roles in CRC were examined using colony formation assays and xenograft mouse models.Results: Expression of tRF5-23-GlyTCC-2 was significantly downregulated in CRC tissues (P = 0.0009) and serum (P < 0.0001) compared to controls. It effectively discriminated CRC patients from healthy individuals and those with colorectal polyps, and served as a strong predictor of poor prognosis. Low tRF5-23-GlyTCC-2 levels were correlated with advanced invasion, metastasis (P = 0.0153), and poor prognosis (P = 0.004). ROC analysis demonstrated its superior diagnostic accuracy over traditional biomarkers (AUC = 0.8628), and its combination with CEA further improved the diagnostic performance (AUC = 0.9077). Both in vitro colony formation assays and in vivo xenograft models confirmed its tumor-suppressive function by inhibiting tumor growth and progression.Conclusion: Serum tRF5-23-GlyTCC-2 exhibits high diagnostic accuracy, and its combination with CEA achieves superior sensitivity (84%), highlighting its potential as a powerful non-invasive biomarker to improve CRC detection and prognosis prediction. Keywords: colorectal cancer, tsRNA, biomarker, carcinostasis, diagnosis

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SHILAP Revista de lepidopterología
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2025-10-01
Primary Topic
Cancer-related molecular mechanisms research
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article

Serum tRF5-23-GlyTCC-2 Functions as a Tumor Suppressor and Novel Biomarker for Colorectal Cancer

SHILAP Revista de lepidopterología
Cancer-related molecular mechanisms research
article

Serum tRF5-23-GlyTCC-2 Functions as a Tumor Suppressor and Novel Biomarker for Colorectal Cancer

article en

Abstract

Xinhui Lv,1,2 Hui Dai,1,2 Yu Wu,1,2 Jiyuan Yang,1,2 Guihua Wang,1,2 Xudong Wang1,2 1Department of Laboratory Medicine, Affiliated Hospital of Nantong University, Nantong, Jiangsu, People’s Republic of China; 2Medical School of Nantong University, Nantong, Jiangsu, People’s Republic of ChinaCorrespondence: Xudong Wang, Department of Laboratory Medicine, Affiliated Hospital of Nantong University, Medical School of Nantong University, Nantong, Jiangsu, 226001, People’s Republic of China, Tel +86-13951318000, Email [email protected]: Transfer RNA-derived small RNAs (tsRNAs) are a recently discovered class of non-coding RNAs with aberrant expression in various cancers. Substantial evidence implicates tsRNAs in the initiation and progression of colorectal cancer (CRC). This study aimed to investigate the diagnostic and prognostic potential of a specific tsRNA, tRF5-23-GlyTCC-2, in CRC.Methods: We identified tRF5-23-GlyTCC-2 via high-throughput RNA sequencing and validated its expression using qRT-PCR. Associations between tRF5-23-GlyTCC-2 expression, clinicopathological features, and patient survival were assessed with Chi-square and Kaplan-Meier analyses. Its diagnostic performance was evaluated by ROC curve analysis. Functional roles in CRC were examined using colony formation assays and xenograft mouse models.Results: Expression of tRF5-23-GlyTCC-2 was significantly downregulated in CRC tissues (P = 0.0009) and serum (P < 0.0001) compared to controls. It effectively discriminated CRC patients from healthy individuals and those with colorectal polyps, and served as a strong predictor of poor prognosis. Low tRF5-23-GlyTCC-2 levels were correlated with advanced invasion, metastasis (P = 0.0153), and poor prognosis (P = 0.004). ROC analysis demonstrated its superior diagnostic accuracy over traditional biomarkers (AUC = 0.8628), and its combination with CEA further improved the diagnostic performance (AUC = 0.9077). Both in vitro colony formation assays and in vivo xenograft models confirmed its tumor-suppressive function by inhibiting tumor growth and progression.Conclusion: Serum tRF5-23-GlyTCC-2 exhibits high diagnostic accuracy, and its combination with CEA achieves superior sensitivity (84%), highlighting its potential as a powerful non-invasive biomarker to improve CRC detection and prognosis prediction. Keywords: colorectal cancer, tsRNA, biomarker, carcinostasis, diagnosis

SHILAP Revista de lepidopterología
Nantong University (CN)
Openalex Percentile: Top 39%
Cancer-related molecular mechanisms research
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