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Single-cell RNA Sequencing Resolves the Regulatory Role of HBV on the Hepatocellular Carcinoma Immune Microenvironment

Single-cell RNA Sequencing Resolves the Regulatory Role of HBV on the Hepatocellular Carcinoma Immune Microenvironment

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05677724
Enrollment
20
Registered
2023-01-10
Start date
2022-07-01
Completion date
2023-06-30
Last updated
2023-01-10

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

Conditions

HBV, Primary Liver Cancer

Brief summary

In summary, with the help of single-cell sequencing technology, this study aims to focus on elucidating the influence of HBV-induced hepatocellular carcinoma cell metabolic changes on microenvironment remodeling. With the help of hepatocellular carcinoma microenvironment changes, this study provide a more accurate diagnosis and treatment method for HBV-induced hepatocellular carcinoma.

Interventions

DIAGNOSTIC_TESTHBV DNA Sequencing

Clinical surgical specimens were obtained, cleaned briefly and transported to the laboratory. Single-cell suspension preparation and blood cell separation were performed, single-cell sorting suspension was prepared and put on the machine, sorting and library construction were performed, and mRNA sequencing adaptor was docked. Single cell data analysis. Based on the findings of single cell analysis, functional verification tests of tumor immune microenvironment cell groups and functional changes of tumor cells were designed.

Sponsors

Fubing Wang
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* Patients with primary liver cancer (hepatocellular carcinoma (HCC)), with evidence of histological or cytological diagnosis, or with HCC meeting conventional clinical diagnostic criteria. * Both sexes, aged 18-80 years old * The results of HBVDNA test were in line with the inclusion criteria * The patient had at least one measurable lesion according to the Response Evaluation Criteria in Solid Tumors, version 1.1 (RECIST V1.1) * Agreed to comply with the study protocol for treatment and follow-up, agreed to provide clinicopathological and follow-up data required by the study, and agreed to use the study data for subsequent research and product development

Exclusion criteria

* Other malignant tumors; * Patients with severe organic diseases do not meet the requirements of infectious liver cancer in this study; * Suffering from mental illness cannot guarantee the compliance of this study; * Previous recipients of any cell or organ transplantation; * Received local regional liver therapy (including various ablations, percutaneous ethanol or acetic acid injections, high-intensity focused ultrasound, transarterial embolization, chemotherapy, or chemoembolization plus embolization) within 14 days prior to study treatment initiation.

Design outcomes

Primary

MeasureTime frameDescription
single cell RNA sequencingwithin 4 hours after the sample was submitted for examination10x genomics chromium 3' sequencing
Biochemical index detectionwithin 4 hours after the sample was submitted for examinationHbsAg (IU/mL) \\HbsAb (mIU/mL)\\HbeAg\\HbeAb\\HbcAb
HBV DNA copy numberwithin 24 hours after the sample was submitted for examinationHBV DNA (IU/mL)

Countries

China

Contacts

Primary ContactFubing Wang, Doctor
wfb20042002@sina.com86-15872385253

Outcome results

None listed

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