Small peptide for inhibiting solid tumor and leukaemia cancer cell growth and use thereof
A technology for cancer cells and leukemia, applied in the field of biotechnology and medicine, can solve the problems of pain, death, damage to normal cells of patients, 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 three kinds of amino acids at the J position: Pro, Asn or Ala; these three kinds of amino acids can be single Placed 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, and the same is true fo...
Embodiment 1
[0036] Test of inhibiting liver cancer cells (synthesis of the short peptide involved in the present invention: Pro-Ala-Leu-Asn-Thr-Val-Lys)
[0037] The human liver cancer cell line Hepg2 cells were cultured with RPMI 1640 medium containing 10% newborn bovine serum, with 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, 48, and 72 hours, The survival rate of living cells was tested by MTT method, and the inhibition rate of liver cancer cells was obtained by comparing the administration group with the control group. Such as figure 1 shown.
Embodiment 2
[0039] 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: Pro-Ala-Serp-Asn-Thr-Val-Lys)
[0040] 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 is planted into a 24-well cell plate, the short peptides involved in the present invention are immediately added to the cell culture plate according to different concentrations, and an equal volume of PBS is used as a control group. The experimental results show that the cells in the 5 days The inhibition rate reached 80%.
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