Identification and Prognostic Value of Key Genes in Hepatocellular Carcinoma

NCT ID: NCT05759858

Last Updated: 2023-03-08

Basic Information

• Recruitment Status: RECRUITING
• Total Enrollment: 100 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2022-12-14
• Study Completion Date: 2025-12-31

Brief Summary

To explore the key genes of human and mouse hepatocellular carcinoma, identify the key genes and prognostic markers, and develop small molecule drugs targeting the key genes to treat hepatocellular carcinoma.

Detailed Description

Hepatocellular carcinoma (HCC) is one of the most common solid malignant tumors and the main cause of cancer-related deaths worldwide. About 750000 new cases of liver cancer are diagnosed every year, half of which are in China. The onset of liver cancer is relatively hidden, and there are generally no symptoms in the early stage. When the patient has obvious clinical symptoms, the disease often belongs to the middle and late stages. The first symptom of liver cancer is liver pain, followed by upper abdominal mass. Some patients also showed some complications of liver cirrhosis, such as black stool, hematemesis, jaundice, liver coma, ascites, etc. A few patients were hospitalized due to symptoms caused by metastatic lesions.

At present, the accuracy of detecting HCC is poor, and the common indicators such as AFP have a certain time lag, which cannot detect patients with liver cancer early. thus, there is an urgent need for a new biomarker for the diagnosis and prognosis of liver cancer. Our research focuses on exploring the key genes of human and mouse hepatocellular carcinoma, identifying the key genes and prognostic markers by means of transcriptome sequencing, and developing small molecule drugs targeting the key genes.

High-throughput sequencing technology was used for sequencing analysis to reflect the expression level of mRNA, small RNA, noncoding RNA, or some other markers. After finding the gene difference between the liver cancer sample and the para-cancer sample, relevant immunohistochemical staining was performed to analyze the overall survival time difference between the patients with high-expression genomes and the patients with low-expression genomes. Follow-up cell and animal experiments were carried out to further verify the effect of target genes on the occurrence and development of liver cancer. In the first month after the operation, the patient was followed up at the outpatient clinic to understand the general situation of the patient after the operation, such as diet and appetite, symptom control, such as fever, abdominal pain, and drainage tube removal. One year and three years after the operation, our center will follow up on the patients and re-hospitalization if necessary.

Conditions

Hepatocellular Carcinoma

Study Design

• Observational Model Type: COHORT
• Study Time Perspective: PROSPECTIVE

Study Groups

Patients with hepatocellular carcinoma confirmed by pathology.

Patients with hepatocellular carcinoma confirmed by pathology.

None of intervention

Intervention Type: OTHER

None of the interventions was applied.

Interventions

None of intervention

None of the interventions was applied.

Intervention Type: OTHER

Eligibility Criteria

Inclusion Criteria

1. Hepatocellular carcinoma confirmed by pathology;

2. The patient has no combined organic diseases of heart, lung, and kidney, etc;

3. No history of chemotherapy, radiotherapy, upper abdominal surgery, or combined with other tumors;

4. The patient has successfully completed the operation and has complete clinical information and pathological data.

Exclusion Criteria

1. Patients who have previous history of other tumors or have undergone upper abdominal surgery;

2. Patients with multiple lesions and distant metastasis;

3. Patients who are complicated with organic diseases of important organs such as heart, lung and kidney and cannot tolerate surgery；

4. Patients who are more than 75 years old or less than 18 years old.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 75 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Second Affiliated Hospital, School of Medicine, Zhejiang University

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Sheng Yan, Doctor

Role: STUDY_CHAIR

2nd Affiliated Hospital, School of Medicine, Zhejiang University, China

Yang Tian, Doctor

Role: STUDY_DIRECTOR

2nd Affiliated Hospital, School of Medicine, Zhejiang University, China

Yuancong Jiang, Doctor

Role: PRINCIPAL_INVESTIGATOR

2nd Affiliated Hospital, School of Medicine, Zhejiang University, China

Locations

2nd Affiliated Hospital, School of Medicine, Zhejiang University

Hangzhou, Zhejiang, China

Site Status: RECRUITING

Countries

China

Central Contacts

Sheng Yan, Doctor

Role: CONTACT

shengyan@zju.edu.cn

13957161680

Yang Tian, Doctor

Role: CONTACT

15088673780

Facility Contacts

Yang Tian, Doctor

Role: primary

15088673780

Yuancong Jiang, Doctor

Role: backup

jiangyuancong@zju.edu.cn

18868107327

Other Identifiers

2022-0856

Identifier Type: -

Identifier Source: org_study_id