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Commentary Open Access
Volume 3 | Issue 1 | DOI: https://doi.org/10.46439/pathology.3.010

FEN1 drives small cell neuroendocrine carcinoma of the cervix progression and holds promise as a therapeutic target

  • 1Shanxi Medical University, School of Basic Medical Sciences, Taiyuan, 030001, China
  • 2The Second Hospital of Shanxi Medical University, Departments of Obstetrics and Gynecology, Taiyuan, 036000, China
  • 3Shanxi Key Laboratory of Functional Proteins, Shanxi Medical University, Taiyuan, 030001, China
  • 4Shanxi Province Cancer Hospital, Department of Pathology, Taiyuan, 030013, China
+ Affiliations - Affiliations

Corresponding Author

Jianbing Liu; liujianbing@sxmu.edu.cn

Received Date: October 30, 2025

Accepted Date: January 07, 2026

Abstract

Small cell neuroendocrine carcinoma of the cervix (SCNECC) is a rare and clinically aggressive subtype of cervical cancer associated with a poor prognosis. To investigate its underlying pathological mechanisms and identify potential therapeutic targets, researchers have increasingly employed single-omics or multi-omics integrated analysis, including single-cell transcriptome sequencing, proteomics, whole-exome sequencing, and genomics. In a study by Jianbing Liu et al., proteomic profiling of SCNECC tumor tissues and adjacent non-tumor tissues revealed that FEN1 drives disease progression by modulating PCNA expression. FEN1 shows promise as a novel therapeutic target for SCNECC. This commentary emphasizes that omics technology is an effective research approach for investigating the pathological mechanisms of SCNECC, and FEN1 shows potential as a novel therapeutic target for SCNECC. However, further experiments are required to elucidate its mechanisms of action.

Keywords

Small cell neuroendocrine carcinoma of the cervix, SCNECC, Proteomics, FEN1, Targeted therapy

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