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Clinicopathological Validation of GPR107-Mediated Regulation of Prostate Cancer Metastasis

Clinicopathological Validation of GPR107-Mediated Regulation of Prostate Cancer Metastasis

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600126844
Enrollment
Unknown
Registered
2026-06-17
Start date
2026-06-30
Completion date
Unknown
Last updated
2026-06-22

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

Conditions

prostate cancer

Interventions

prostate cancer patient:None

Sponsors

Chengdu Integrated TCM and Western Medicine Hospital
Lead Sponsor

Eligibility

Sex/Gender
Male

Inclusion criteria

Inclusion criteria: 1. Cases with a previous pathological diagnosis of prostate cancer; 2. Available FFPE prostate cancer tissue samples from which consecutive tissue sections can be prepared for this study; 3. Tissue samples with adequate preservation quality and intact tissue structure, suitable for immunohistochemistry and multiplex immunofluorescence analyses; 4. Available clinicopathological information relevant to this study, including but not limited to Gleason score, tumor stage, metastatic status, PSA level, lesion extent, or histological subtype; 5. Samples and related data have been de-identified or coded, and their use is within the scope of ethics approval or ethics filing;

Exclusion criteria

Exclusion criteria: 1. Non-prostate cancer cases or cases without a definite pathological diagnosis; 2. FFPE tissue samples with poor preservation quality, severe tissue damage, section detachment, or extensive necrosis, making them unsuitable for immunohistochemistry or multiplex immunofluorescence analyses; 3. Cases with insufficient consecutive tissue sections to complete the planned study assays; 4. Cases with missing key clinicopathological information required for the main correlation analyses; 5. Samples with unclear numbering, source, or transfer information, preventing the establishment of a traceable but de-identified correspondence; 6. Samples not covered by the ethics approval or ethics filing, or samples from patients who explicitly refused the use of their specimens for research;

Design outcomes

Primary

MeasureTime frame
Subcellular localization of G protein-coupled receptor 107 (GPR107) protein and its specific post-translational modification site in prostate cancer tissues;Expression level of G protein-coupled receptor 107 (GPR107) protein in prostate cancer tissues;Expression level of the specific post-translational modification site of G protein-coupled receptor 107 (GPR107) in prostate cancer tissues;Expression trends of G protein-coupled receptor 107 (GPR107) and its specific post-translational modification site across pathological subgroups;Tumor staging; metastatic status;Co-expression of G protein-coupled receptor 107 (GPR107), its specific post-translational modification site, and key target proteins in prostate cancer tissues;Spatial co-localization of G protein-coupled receptor 107 (GPR107), its specific post-translational modification site, and key target proteins in prostate cancer tissues;

Secondary

MeasureTime frame
Inter-case differences in the expression level of G protein-coupled receptor 107 (GPR107) protein;Expression trends of G protein-coupled receptor 107 (GPR107) and its specific post-translational modification site across pathological subgroups;Staining specificity, stability, and applicability of the relevant antibodies in formalin-fixed paraffin-embedded (FFPE) prostate cancer tissues;Spatial distribution pattern of target molecules in prostate cancer tissues based on multiplex immunofluorescence (mIF) images;

Countries

China

Contacts

Public ContactLiang Yuqing

Chengdu Integrated Traditional Chinese and Western Medicine Hospital

yuqing-liang@foxmail.com+86 28 8531 1468

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jun 29, 2026