Short peptide suppressing growth of cancer cell and uses thereof
A technology of cancer cells and short peptides, applied in the field of biotechnology and medicine, can solve problems such as patient pain, death, chemotherapy drug bone marrow suppression, etc., and achieve the effect of solving serious injuries
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[0018] The preparation method of the short peptide adopts a chemical synthesis method, that is, a very mature solid-phase peptide synthesis method well known in the art, and either the Boc method or the Fmoc method can be used. The specific method is to couple the protected amino acids to the inert solid phase carrier one by one, and then use strong acid to cleave the peptide chain from the carrier, and remove the side chain protection at the same time.
[0019] The main amino acid sequence of the short peptide is a main sequence with fixed amino acid positions, and the corresponding amino acids are selected and arranged at the interval positions. For example, there are 3 kinds of Lys, Thr or Ile in the amino acid position of the J position, and these 3 kinds of amino acids can be placed in a single place. At the J position in , no matter which one is selected, the short peptide still has its original biological activity, that is, inhibits the growth of malignant tumor cells, a...
Embodiment 1
[0037] Test of inhibiting liver cancer cells (synthesis of the short peptide involved in the present invention: Lys-Leu-Pro-Ser-Ser-Ala-Lys or Lys-Leu-Pro-Ser-Ala-Ala-Lys)
[0038] The culture of the human liver cancer cell line Bel-7402 cells was cultivated with RPMI 1640 medium containing 10% newborn bovine serum, and was cultured at 5×10 5 The cell density per well was planted into a 96-well cell plate. After 24 hours, the short peptides involved in the present invention were added to the cell culture plate according to different concentrations, and an equal volume of PBS was used as the control group. After 24 hours, the cell counting plate was used to Count, compare the administration group with the control group, and obtain the inhibition rate of liver cancer cells. As shown in Figure 1, the short peptide involved in the present invention and the photo taken under the microscope after the joint action of human liver cancer cells for 24 hours, the cells in the administrat...
Embodiment 2
[0040] Inhibition of acute myeloid leukemia (M 2 ) (synthesis of the short peptide derivatives involved in the present invention, modified by adding phosphoric acid group at serine: Thr-Leu-Pro-Serp-Ala-Ala-Lys)
[0041] Human acute myeloid leukemia cell line HL60 cells were cultured with RPMI 1640 medium containing 10% newborn bovine serum, and cultured in 10 6 After the cell density per well was planted into a 24-well cell plate, the short peptides involved in the present invention were immediately added to the cell culture plate according to different concentrations, and an equal volume of PBS was used as a control group. The existing clinical drug As 2 o 3 As a positive control, after 24 hours, through flow cytometry detection (FACS), the experimental results are as follows figure 2 As shown, the right upper limit 59.32% represents the number of dead cells, 38.91% represents the number of early apoptotic cells, and the total effective rate of cell inhibition exceeds 98%...
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