» Articles » PMID: 31186765

Urinary Biomarkers for the Diagnosis of Cervical Cancer by Quantitative Label-free Mass Spectrometry Analysis

Abstract

Due to the invasive procedure associated with Pap smears for diagnosing cervical cancer and the conservative culture of developing countries, identifying less invasive biomarkers is of great interest. Quantitative label-free mass spectrometry was performed to identify potential biomarkers in the urine samples of patients with cervical cancer. This technique was used to study the differential expression of urinary proteomes between normal individuals and cancer patients. The alterations in the levels of urinary proteomes in normal and cancer patients were analyzed by Progenesis label-free software and the results revealed that 60 proteins were upregulated while 73 proteins were downregulated in patients with cervical cancer. This method could enrich high molecular weight proteins from 100 kDa. The protein-protein interactions were obtained by Search Tool for the Retrieval of Interacting Genes/Proteins analysis and predicted the biological pathways involving various functions including cell-cell adhesion, blood coagulation, metabolic processes, stress response and the regulation of morphogenesis. Two notable upregulated urinary proteins were leucine-rich α-2-glycoprotein (LRG1) and isoform-1 of multimerin-1 (MMRN1), while the 3 notable downregulated proteins were S100 calcium-binding protein A8 (S100A8), serpin B3 (SERPINB3) and cluster of differentiation-44 antigen (CD44). The validation of these 5 proteins was performed by western blot analysis and the biomarker sensitivity of these proteins was analyzed individually and in combination with receiver operator characteristic curve (ROC) analysis. Quantitative mass spectrometry analysis may allow for the identification of urinary proteins of high molecular weight. The proteins MMRN1 and LRG1 were presented, for the first time, to be highly expressed urinary proteins in cervical cancer. ROC analysis revealed that LRG1 and SERPINB3 could be individually used, and these 5 proteins could also be combined, to detect the occurrence of cervical cancer.

Citing Articles

Advances in S100 protein family for gynecological malignancies.

Wu S, Xu J Discov Oncol. 2025; 16(1):287.

PMID: 40057924 PMC: 11891126. DOI: 10.1007/s12672-025-02028-x.


Recent progress in mass spectrometry-based urinary proteomics.

Joshi N, Garapati K, Ghose V, Kandasamy R, Pandey A Clin Proteomics. 2024; 21(1):14.

PMID: 38389064 PMC: 10885485. DOI: 10.1186/s12014-024-09462-z.


Unveiling diagnostic and therapeutic strategies for cervical cancer: biomarker discovery through proteomics approaches and exploring the role of cervical cancer stem cells.

Jafari A, Farahani M, Abdollahpour-Alitappeh M, Manzari-Tavakoli A, Yazdani M, Rezaei-Tavirani M Front Oncol. 2024; 13:1277772.

PMID: 38328436 PMC: 10847843. DOI: 10.3389/fonc.2023.1277772.


Searching for the methylation sites involved in human papillomavirus type 16 and 18‑positive women with cervical cancer.

Ma Y, Wang C, Shi M, Li M, Li L, Che T Mol Clin Oncol. 2022; 17(4):149.

PMID: 36157320 PMC: 9468798. DOI: 10.3892/mco.2022.2582.


Exploration of biomarkers for the diagnosis, treatment and prognosis of cervical cancer: a review.

Arip M, Tan L, Jayaraj R, Abdullah M, Rajagopal M, Selvaraja M Discov Oncol. 2022; 13(1):91.

PMID: 36152065 PMC: 9509511. DOI: 10.1007/s12672-022-00551-9.


References
1.
Wobus M, Kuns R, Wolf C, Horn L, Kohler U, Sheyn I . CD44 mediates constitutive type I receptor signaling in cervical carcinoma cells. Gynecol Oncol. 2001; 83(2):227-34. DOI: 10.1006/gyno.2001.6369. View

2.
Ott H, Lindner H, Sarg B, Mueller-Holzner E, Abendstein B, Bergant A . Calgranulins in cystic fluid and serum from patients with ovarian carcinomas. Cancer Res. 2003; 63(21):7507-14. View

3.
Apgar B, Zoschnick L, Wright Jr T . The 2001 Bethesda System terminology. Am Fam Physician. 2003; 68(10):1992-8. View

4.
Wang J, Cai Y, Xu H, Zhao J, Xu X, Han Y . Expression of MRP14 gene is frequently down-regulated in Chinese human esophageal cancer. Cell Res. 2004; 14(1):46-53. DOI: 10.1038/sj.cr.7290201. View

5.
Kong J, Ding F, Zhou C, Wang X, Miao X, Wu M . Loss of myeloid-related proteins 8 and myeloid-related proteins 14 expression in human esophageal squamous cell carcinoma correlates with poor differentiation. World J Gastroenterol. 2004; 10(8):1093-7. PMC: 4656340. DOI: 10.3748/wjg.v10.i8.1093. View