Short peptide for inhibiting growth of solid tumor and leukemia cancer cells and application thereof
A cancer cell, short peptide technology, applied in the field of biotechnology and medicine, can solve the problems of patient suffering, chemotherapy drugs myelosuppression, damage to patients' normal cells, etc., to achieve the effect of solving serious injuries
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[0016] 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.
[0017] 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 amino acids at the J position: Pro, Leu or Ile; these 3 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 for the am...
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[0032] Below in conjunction with embodiment, further set forth the present invention. These implementation examples are only used to illustrate the present invention and are not intended to limit the scope of the present invention.
[0033] All synthetic short peptides involved in all the following enumerated examples have the pharmaceutical functions involved in the present invention and are not limited to the enumerated functions.
Embodiment 1
[0035] Test of inhibiting liver cancer cells (synthesis of the short peptide involved in the present invention: Pro-Gly-Val-Tyr-Thr-Lys)
[0036] The culture of human liver cancer cell line HepG2 cells was cultivated with RPMI 1640 medium containing 10% newborn bovine serum, with 10 4 The cell density per well was planted into a 96-well cell plate. After 24 hours, the short peptides involved in this experiment 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 absorbance was detected in a microplate reader by the MTT method at 570 nm. Compared with the control group, the inhibition rates of liver cancer cells were obtained. The inhibition rates of high-concentration PK-6 were 5.01%, 29.62% and 46.96%, respectively, and the inhibition rates of low-concentration PK-6 were 16.53%, 30.40% and 28.97%. . like figure 1 shown.
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