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The Predictive Value of Serum Histone Succinylation in Malignant Solid Tumors

Serum Histone Succinylation: A Predictive Biomarker for Malignant Solid Tumors

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07132606
Enrollment
1000
Registered
2025-08-20
Start date
2025-08-20
Completion date
2026-08-01
Last updated
2025-08-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Malignant Tumors

Brief summary

In recent years, advances in protein post-translational modification (PTM) research have revealed histone succinylation as a novel epigenetic modification mechanism critically involved in tumor initiation, progression, and prognosis. Succinylation alters protein physicochemical properties and functions, thereby modulating cellular metabolism, proliferation, and apoptosis. Aberrant histone succinylation in tumor cells demonstrates significant correlations with tumor type, staging, and clinical outcomes, offering new avenues for early cancer diagnosis. This project utilizes blood serum samples to quantify histone succinylation levels through modification-specific antibody-based detection. Integrated with clinical data, this approach enables early, rapid, and accurate pan-cancer diagnosis, achieving tumor screening via a single-tube blood test. It represents a paradigm shift in precision oncology from gene-driven to epigenetic-metabolic-driven early detection.

Detailed description

Primary Objective To evaluate differential expression of serum histone succinylation between malignant solid tumor patients and healthy controls, thereby validating its early detection value. Secondary Objectives To determine correlations between serum histone succinylation levels and: Tumor types Tumor stages To statistically analyze associations of serum histone succinylation with: Therapeutic efficacy (surgical intervention, radiotherapy, systemic therapy) Clinicopathological variables

Interventions

None listed

Sponsors

Yinghua Ji
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

Case Group: * Aged ≥18 years, regardless of sex; * Histologically or cytologically confirmed malignant solid tumors requiring subsequent anticancer therapy; Control Group: * Aged ≥18 years, regardless of sex; * Non-cancer participants enrolled through health screenings;

Exclusion criteria

* Pregnant individuals; * Individuals with serious mental disorders or communication barriers; * Other conditions deemed by investigators to contraindicate study participation;

Design outcomes

Primary

MeasureTime frameDescription
Evaluate the positive rate of serum histone succinylation in patients with malignant solid tumors2025.08.01-2026.12.31Evaluate the positive rate of serum histone succinylation in malignant solid tumor patients versus healthy individuals through Western blot analysis, quantify the percentage difference between the two groups, and thereby validate its potential for early cancer screening

Secondary

MeasureTime frameDescription
Define the relationship between histone succinylation modifications in serum and different tumor types as well as tumor staging2025.08.01-2026.12.31Analyze the relationship between histone succinylation modifications in serum and therapeutic efficacy (specifically surgery, radiotherapy, and systemic therapy)。

Contacts

Primary ContactWang Fang Doctor, Graduate Student
583573667@qq.com18337312280

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026