Diet controlled expression of a nucleic acid encoding a pro-apoptotic protein
A nucleic acid for the controlled expression of a nucleic acid encoding a pro-apoptotic protein in an individual, including: a regulatory polynucleotide including a minimal promoter and at least one AARE (amino acid response element) nucleic acid, the regulatory polynucleotide being activated in an individual upon consumption of a diet deficient in at least one essential amino acid; and a nucleic acid encoding a pro-apoptotic protein, which is placed under the control of the regulatory polynucleotide.
1. A method for eliminating infused cells which contain a nucleic acid comprising:
a regulatory polynucleotide comprising a minimal promoter and at least one AARE (amino acid response element) nucleic acid, the regulatory polynucleotide being activated in a human individual upon consumption of a diet deficient in at least one essential amino acid; and
a suicide safety gene selected from the group consisting of: BCL2 modifying factor, Apoptosis inducer NBK, Apoptotic protease-activating factor 1 (APAF1, CED4), BAX, Endophilin B1, FADD, CRADD, FAS, Modulator of apoptosis 1, SMAC, Endonuclease G, HRK, Serine protease HTRA2, p53, NOXA, RIPK1, Bcl2 binding component 3, PMAIP1, Tumor necrosis factor receptor superfamily member 10A Precursor (Death receptor 4), caspase 1, caspase 3, caspase 7, caspase 8, and caspase 9, the product of which is associated with the killing of cells, said suicide safety gene being placed under the control of the regulatory polynucleotide, the method comprising:
a) administering the infused cells to a human individual in need of cancer treatment or regenerative medicine, and then
b) eliminating the infused cells by inducing programmed cellular death into at least one of the infused cells by submitting the human individual to a diet deficient in at least one essential amino acid.
2. The method according to claim 1 , wherein in the nucleic acid, the amino acid response element (AARE) nucleic acid is a nucleic acid of a sequence selected from the group consisting of SEQ ID No: 1, SEQ ID No: 2, SEQ ID No: 3, SEQ ID No: 4 and SEQ ID No: 5.
3. The method according to claim 1 , wherein in the nucleic acid, the regulatory polynucleotide comprises at least two AARE nucleic acids.
4. The method according to claim 1 , wherein the nucleic acid comprises a suicide gene encoding a protein performing a suicide task, which protein is selected from the group consisting of caspase 1, caspase 3, caspase 7, caspase 8 and caspase 9.
5. The method according to claim 4 , wherein the protein performing a suicide task is caspase 9.
6. The method according to claim 1 , wherein the nucleic acid is comprised in a nucleic acid vector for the controlled expression of a suicide safety gene.
7. The method according to claim 1 , wherein the nucleic acid, or a nucleic acid vector comprising the nucleic acid, is comprised in a delivery particle.
8. The method according to claim 7 , wherein the delivery particle comprises at its surface one or more ligands suitable for binding to a target receptor exposed at the membrane of a targeted cell.
9. The method according to claim 1 , wherein the infused cells are selected from the group consisting of CAR T-cells and stem cells.
10. The method according to claim 1 , wherein the infused cells are stem cells selected from the group consisting of hematopoietic stem cells and iPS cells.