Isoform of bruton's tyrosine kinase (BTK) protein
The use of compounds is described which are capable of functionally blocking at least one of the genes chosen from the group composed of EphAI, EphA2, EphA8, EphB2, CSF1R, VEGFR2, RAMP2, RAMP3, CLRN1, MAPK4, PIK3C2A, PIK3CG, GSK3alpha, GSK3beta, IRAK3, DAPK1, JAK1, PIM1, TRB3, BTG1, LATS1, LIMK2, MYLK, PAK1, PAK2, CDC2, BTK, PNRC2, NCOA4, NR2C1, TPR, RBBP8, TRPC7, FXYD1, ERNI, PRSS16, RPS3, CCL23 and SERPINE1, for the manufacture of a medicament destined to diminish the resistance to chemotherapeutic drugs in the therapeutic treatment of epithelial tumor pathologies. Also described is a method for the determination of the drug resistance in tumor cells, as well as a method for the identification of tumor stem cells.
1. The pharmaceutical composition comprising a compound capable of functionally and selectively blocking the shorter isoform of Bruton's tyrosine kinase (BTK) having the amino acid sequence of SEQ ID NO: 2 and a chemotherapeutic drug for the treatment of epithelial tumours, wherein the compound capable of functionally and selectively blocking BTK comprises
(a) a small interfering RNA (siRNA) or a short hairpin RNA (shRNA) targeting a 5′-untranslated region (5′-UTR) (SEQ ID NO: 1) of a messenger RNA (mRNA) encoding a shorter isoform of Bruton's Tyrosine Kinase (BTK) having the amino acid sequence of SEQ ID NO: 2, wherein the shorter isoform does not contain amino acid residues 1-88 or 2-89 of the Bruton's Tyrosine Kinase (BTK) set forth in SEQ ID NO: 3; and
(b) a pharmaceutically acceptable carrier.
2. The pharmaceutical composition according to claim 1 , wherein the small interfering RNA (siRNA) comprises a double-stranded RNA comprising:
(i) a sense polynucleotide strand having a nucleotide sequence length of from about 19 to about 23 nucleotides, wherein the sense polynucleotide strand is complementary to the 5′-untranslated region (5′-UTR) of the shorter isoform of the Bruton's Tyrosine Kinase (BTK) set forth in SEQ ID NO: 1; and
(ii) an anti-sense polynucleotide strand that is complementary to the sequence of the sense polynucleotide strand.
3. The pharmaceutical composition according to claim 1 , wherein the small hairpin RNA (shRNA) comprises:
(i) a sense polynucleotide strand having a nucleotide sequence length of 19 to 23 nucleotides, wherein the sense polynucleotide strand is complementary to the 5′-untranslated region (5′-UTR) of the shorter isoform of the Bruton's Tyrosine Kinase (BTK) set forth in SEQ ID NO: 1;
(ii) an anti-sense polynucleotide strand that is complementary to the sequence of the sense polynucleotide strand; and
(iii) a polynucleotide linker sequence of sufficient length, wherein the polynucleotide linker sequence allows the sense polynucleotide strand and the anti-sense polynucleotide strand to fold over and hybridize to each other.
4. The pharmaceutical composition according to claim 3 , wherein the small hairpin RNA (shRNA) is expressed by an expression vector.
5. The pharmaceutical composition according to claim 4 , wherein the expression vector is a retroviral vector.
6. The pharmaceutical composition according to claim 1 , wherein the siRNA or the shRNA does not affect expression of Bruton's Tyrosine Kinase (BTK) set forth in SEQ ID NO: 3.
7. The pharmaceutical composition according to claim 1 , wherein the compound capable of functionally blocking the shorter isoform of Bruton's Tyrosine Kinase (BTK) having the amino acid sequence of SEQ ID NO: 2, wherein the shorter isoform does not contain amino acid residues 1-88 or 2-89 of BTK set forth in SEQ ID NO: 3 is at least one agent selected from the group consisting of LFM-A13, AVL-292, Ibrutinib, Dasatinib, Bosutinib, and a combination thereof.
8. The pharmaceutical composition according to claim 1 , wherein said chemotherapeutic drug is at least one selected from the group consisting of an antimetabolite, a DNA-damaging agent, and a combination thereof.
9. The pharmaceutical composition according to claim 8 , wherein the DNA-damaging agent is selected from the group consisting of topoisomerase I inhibitor, a topoisomerase II inhibitor, a platinum coordination compound, an alkylating agent, and a combination thereof.
10. The pharmaceutical composition according to claim 8 , wherein said chemotherapeutic agent is selected from the group consisting of 5-fluorouracil (5-FU), oxaliplatin, and a combination thereof.