TET2 as a diagnostic and prognostic marker in hematopoietic neoplasms
The present invention concerns an in vitro method for diagnosing a myeloid tumour or a lymphoid tumour in a subject, which comprises the step of analyzing a biological sample from said subject by (i) detecting the presence of a mutation in the Ten Eleven Translocation protein family member 2 gene (TET2) coding for the polypeptide having the sequence SEQ ID NO: 2, and/or (ii) analyzing the expression of the TET2 gene; wherein the detection of such a TET2 mutation, of the absence of expression of TET2 or of the expression of a truncated TET2 is indicative of a subject developing or predisposed to develop a myeloid tumour or a lymphoid tumour.
1. A method for detecting a mutated TET2 gene comprising:
(i) obtaining a blood or bone marrow sample of a subject having a myeloid tumour or a lymphoid tumour; and
(ii) detecting that Hematopoietic Stem Cells (HSC) or CD34+/CD38− progenitor cells in said blood or bone marrow sample have a missense mutation 51898F, H1868R, G1869W, or L1872P or a frameshift at Q1834 or L1889 (numbering of SEQ ID NO: 2) by:
a. sequencing a region of the nucleic acid contained in said cells, wherein the region encodes S1898F H1868R, G1869W, or L1872P or a frameshift at Q1834 or L1889, or
b. hybridizing the nucleic acid contained in said cells with at least one probe or primer comprising at least 10 consecutive nucleotides of the region encoding S1898F, H1868R, G1869W, or L1872P or a frameshift at Q1834 or L1889.
2. The method according to claim 1 , wherein said tumour is a myeloid tumour selected from the group consisting of myelodysplastic syndrome (MDS), acute myeloid leukemia (AML), myeloproliferative disease (MPD) and myelodysplatic/myeloproliferative syndrome.
3. The method according to claim 1 , wherein said myeloid tumour is a myelodysplatic/myeloproliferative syndrome.
4. The method according to claim 1 , wherein said tumour is a lymphoid tumour selected from the group consisting of lymphoma.
5. The method according to claim 1 , wherein said subject is suffering from polycythemia vera (PV) or from thrombocythemia (ET).
6. The method according to claim 1 , wherein said subject is suffering from myelodysplastic syndrome (MDS).
7. The method according to claim 1 , wherein said subject is a mammal.
8. The method according to claim 1 , wherein said mutation is detected on both alleles of the mutated TET2 gene.
9. The method of claim 1 , wherein mutation induces absence of expression or under-expression of TET2 polypeptide.
10. The method according to claim 1 , wherein the detecting step al comprises using a kit comprising at least one nucleic acid probe or oligonucleotide or at least one antibody.
11. The method according to claim 10 , wherein said oligonucleotide is at least one PCR primer, which allows amplifying a region of the TET2 gene.
12. The method according to claim 1 , further comprising the step of administering to said subject a therapeutically efficient amount of hypomethylating agent after the detecting step.
13. The method according to claim 1 , wherein said at least one primer is one of SEQ ID NO:5 to SEQ ID NO:38.