TuLip : Role of the Tumor Environment in Cancer-related Fat Loss
- Conditions
- Adipose TissueCancerCachexia
- Interventions
- Procedure: Nissen Fundoplication, cholecystectomy
- Registration Number
- NCT05128318
- Lead Sponsor
- Université Catholique de Louvain
- Brief Summary
Cancer cachexia is defined as a weight loss of more than 5% over the last 6 months, a loss of body fat and muscle atrophy. It is found in 80% of patients with advanced cancer. In this context, white adipose tissue is a particularly interesting target since its depletion precedes the loss of muscle mass, and is sufficient to induce a decrease in the response to anti-cancer treatments and in the survival of patients.
This cachexia is associated with advanced tumors that present acidosis and metastasis. In this clinical study the investigators would like explore the acid environment effect on the human adipose tissue depletion and more specifically on adipocyte lipolysis.
The main objective of the "TuLip" clinical study is therefore to validate in human subcutaneous and visceral adipocytes that factors secreted by tumor cells cultivated in acid tumor environment stimulate the release of lipids from adipose tissue. Adipocytes retrieves from this study will also be used to validate identified potential lipolytic factors derived from these cells.
- Detailed Description
This study is a monocentric clinical study. Patients with BMI \< 30 kg/m2 will be recruited in the context of programmed abdominal surgery. In this context, subcutaneous and visceral adipose tissue pieces (1-2 cm3) will be collected to explore the lypolytic response of adipocytes ex-vivo to factors secreted by human cancer cell lines.
Recruitment & Eligibility
- Status
- TERMINATED
- Sex
- All
- Target Recruitment
- 5
- Programmed surgeries in the abdominal area in the Department of Surgery and Transplantation at Cliniques Universitaires Saint-Luc under the supervision of Prof. Dr. Benoit Navez.
- Hospitalization in the context of surgery
- Caucasian
- Age between 18 and 60 years (included).
- Body mass index less than 30 and greater than or equal to 18.5
- Programmed Nissen fundoplication (to treat hiatal hernia and gastroesophageal reflux) or cholecystectomy (to treat vesicular lithiasis), eventration, or parietal surgery .
- Adults capable of expressing their wishes.
- Understanding French
- Body mass index below 18.5 and above 30.
- Patients with cancer, infection, autoimmune or inflammatory disease, metabolic syndrome.
- Patients with beta-blockers, hypoglycemics, anti-diabetics, hypolipidemics.
- Adults unable to express their will.
- Not understanding French
- Patients participating in a clinical trial for a drug treatment.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description Patients with BMI < 30 kg/m2 Nissen Fundoplication, cholecystectomy Collection of subcutaneous and visceral adipose tissue pieces of 1-2 cm3 during abdominal surgery procedures
- Primary Outcome Measures
Name Time Method Evaluation of the lipolytic response of adipocytes isolated from human visceral and subcutaneous adipose tissue to factors derived from cancer cells in acid environment by the glycerol measurement Up to 100 days after the adipose tissue collection" Measure ex-vivo of the lipolysis of subcutaneous and visceral adipocytes in the presence of factors derived from cancer cells. The lipolysis will be assessed by the measure of glycerol (in mol/L) released by adipocytes.
Evaluation of the lipolytic response of adipocytes isolated from human visceral and subcutaneous adipose tissue to factors derived from cancer cells in acid environment by the fatty acid measurement. Up to 100 days after the adipose tissue collection" Measure ex-vivo of the lipolysis of subcutaneous and visceral adipocytes in the presence of factors derived from cancer cells. The lipolysis will be assessed by the measure of free fatty acids (in mol/L) released by adipocytes.
- Secondary Outcome Measures
Name Time Method Evaluation of the lipid metabolism, of adipocytes isolated from human visceral and subcutaneous adipose tissues to factors derived from cancer cells in acid environment, by proteomic analyses Up to 2 years after the adipose tissue collection Protein analyses via proteomic analyses (relative units).
Evaluation of the lipid metabolism, of adipocytes isolated from human visceral and subcutaneous adipose tissues to factors derived from cancer cells in acid environment, by biochemical analyses Up to 2 years after the adipose tissue collection Biochemical analyses (biochemical kits)
Evaluation of the lipid metabolism, of adipocytes isolated from human visceral and subcutaneous adipose tissues to factors derived from cancer cells in acid environment, by RT-qPCR Up to 2 years after the adipose tissue collection Measurement of gene expression by RT-qPCR (in relative units) of RNA extracted from these ex-vivo cultured human adipocytes.
Evaluation of the lipid metabolism, of adipocytes isolated from human visceral and subcutaneous adipose tissues to factors derived from cancer cells in acid environment, by RNA sequencing Up to 2 years after the adipose tissue collection Measurement of gene expression by RNA sequencing (in counts) of RNA extracted from these ex-vivo cultured human adipocytes.
Evaluation of the lipid metabolism, of adipocytes isolated from human visceral and subcutaneous adipose tissues to factors derived from cancer cells in acid environment, by western-blot Up to 2 years after the adipose tissue collection Protein analyses by western-blot (arbitrary units).
Evaluation of the lipid metabolism, of adipocytes isolated from human visceral and subcutaneous adipose tissues to factors derived from cancer cells in acid environment, by ELISA Up to 2 years after the adipose tissue collection Protein analyses by ELISA (mol/L or g/L).
Evaluation of the lipid metabolism, of adipocytes isolated from human visceral and subcutaneous adipose tissues to factors derived from cancer cells in acid environment, by metabolomic analyses Up to 2 years after the adipose tissue collection Metabolomic analyses (arbitrary units or mol/L)
Trial Locations
- Locations (1)
Cliniques universitaires Saint Luc
🇧🇪Brussel, Belgium