FIELD: pharmaceutical industry.
SUBSTANCE: present group of inventions refers to a method of treating cancer characterized by expressing a mutation form of RAS protein. Method of treating cancer characterized by expression of mutant form of RAS protein, involving introduction of Plinabulin to a subject, wherein the mutant form of the RAS protein is a mutant form of the NRAS protein, a mutant form of the HRAS protein or a mutant form of the KRAS protein, which contains one or more amino acid substitutions G12C, G12R, G12D, G12V, G12F, G12L, G12N, G13C, G13R, G13S, G13A, G13V, G13P, S17G, P34S, A59E, A59G, A59T, Q61K, Q61L, Q61R, Q61H, K117N, A146P, A146T, A146V and D153V. A method for inhibiting cell proliferation with a RAS mutation, involving bringing said cell into contact with a Plinabulin, wherein the mutant form of the RAS protein is a mutant form of the NRAS protein, a mutant form of the HRAS protein or a mutant form of the KRAS protein, which contains one or more amino acid substitutions selected from the group G12C, G12R, G12D, G12V, G12F, G12L, G12N, G13C, G13R, G13S, G13A, G13V, G13P, S17G, P34S, A59E, A59G, A59T, Q61K, Q61L, Q61R, Q61H, K117N, A146P, A146T, A146V and D153V. A method for inducing apoptosis in a cell containing a RAS mutation, involving bringing said cell into contact with a Plinabulin, wherein the mutant form of the RAS protein is a mutant form of the NRAS protein, a mutant form of the HRAS protein or a mutant form of the KRAS protein, which contains one or more amino acid substitutions G12C, G12R, G12D, G12V, G12F, G12L, G12N, G13C, G13R, G13S, G13A, G13V, G13P, S17G, P34S, A59E, A59G, A59T, Q61K, Q61L, Q61R, Q61H, K117N, A146P, A146T, A146V and D153V. A method for inhibiting the progression of cancer characterized by expression of a mutant form of RAS protein in a subject, involving administering Plinabulin to a subject, wherein the mutant form of the RAS protein is a mutant form of the NRAS protein, a mutant form of the HRAS protein or a mutant form of the KRAS protein, which contains one or more amino acid substitutions selected from the group G12C, G12R, G12D, G12V, G12F, G12L, G12N, G13C, G13R, G13S, G13A, G13V, G13P, S17G, P34S, A59E, A59G, A59T, Q61K, Q61L, Q61R, Q61H, K117N, A146P, A146T, A146V and D153V.
EFFECT: disclosed methods are effective methods of treating cancer associated with a mutation of oncogenic RAS genes.
26 cl, 7 dwg, 2 tbl, 6 ex
Title | Year | Author | Number |
---|---|---|---|
COMBINATION THERAPY | 2018 |
|
RU2815400C2 |
METHOD FOR TREATING A BRAIN TUMOR | 2016 |
|
RU2728796C2 |
THERAPEUTIC COMBINATIONS CONTAINING RAF INHIBITOR AND ERK INHIBITOR | 2017 |
|
RU2774612C2 |
PEPTIDE VACCINE COMPRISING RAS PEPTIDE CONTAINING MUTATIONS, AND CHEMOTHERAPEUTIC AGENT | 2015 |
|
RU2700929C2 |
TREATING PATIENTS DIAGNOSED WITH PANCREATIC DUCT ADENOCARCINOMA WITH USING EPIDERMAL GROWTH FACTOR (EGFR) RECEPTOR MONOCLONAL ANTIBODIES | 2016 |
|
RU2728571C2 |
METHODS AND COMBINED THERAPEUTIC PRODUCT FOR THE TREATMENT OF BILE DUCTS CANCER | 2019 |
|
RU2793543C2 |
COMBINATION OF EGFR INHIBITOR AND MEK INHIBITOR FOR USE IN TREATMENT OF NRAS MUTATED CANCER | 2015 |
|
RU2683276C2 |
COMBINATION THERAPY | 2013 |
|
RU2677245C2 |
PHARMACEUTICAL COMPOUND | 2018 |
|
RU2786994C2 |
COMPOSITIONS BASED ON SHP2 INHIBITOR AND METHODS OF CANCER TREATMENT | 2018 |
|
RU2805355C2 |
Authors
Dates
2020-11-11—Published
2016-03-02—Filed