MicroRNA fingerprints during human megakaryocytopoiesis
The present invention provides novel methods and compositions for the diagnosis, prognosis and treatment of cancer and myeloproliferative disorders. The invention also provides methods of identifying anti-cancer agents.
1. A method of diagnosing acute megakaryoblastic leukemia in a subject, comprising:
i) comparing the level of at least one miR-155 gene product in a subject sample to control; and
ii) diagnosing acute megakaryoblastic leukemia in the event that the at least one miR-155 gene product level is lower in the sample compared to control.
2. The method of claim 1 , wherein the control is the level of the at least one miR-155 gene product from a subject that does not have a acute megakaryoblastic leukemia disorder.
3. The method of claim 1 , wherein the subject is a human.
4. The method of claim 1 , wherein the control is the level of the at least one miR-155 gene product from a reference sample comprising non-differentiating megakaryocyte progeny and/or megakaryocytes.
5. The method of claim 1 , which further comprises:
i) comparing the level of at least one additional miR gene product in a subject sample to control, wherein the at least one additional miR gene product is selected from the group consisting of: miR-101; miR-126; miR-99a; miR-99-prec; miR-106; miR-339; miR-99b; miR-149; miR-33; miR-135; and miR-20; and
ii) diagnosing acute megakaryoblastic leukemia in the event that the at least one additional miR gene product level is higher in the sample compared to control.
6. A method of diagnosing acute megakaryoblastic leukemia in a subject, comprising:
i) comparing the level of at least one miR-140 gene product in a subject sample to control; and
ii) diagnosing acute megakaryoblastic leukemia in the event that the at least one miR-140 gene product level is lower in the sample compared to control.
7. The method of claim 6 , wherein the control is the level of the at least one miR-140 gene product from a subject that does not have a acute megakaryoblastic leukemia disorder.
8. The method of claim 6 , wherein the subject is a human.
9. The method of claim 6 , wherein the control is the level of the at least one miR-140 gene product from a reference sample comprising non-differentiating megakaryocyte progeny and/or megakaryocytes.
10. The method of claim 6 , which further comprises:
i) comparing the level of at least one additional miR gene product in a subject sample to control, wherein the at least one additional miR gene product is selected from the group consisting of: miR-101; miR-126; miR-99a; miR-99-prec; miR-106; miR-339; miR-99b; miR-149; miR-33; miR-135; and miR-20; and
ii) diagnosing acute megakaryoblastic leukemia in the event that the at least one miR gene product level is higher in the sample compared to control.
11. A method of diagnosing-acute megakaryoblastic leukemia in a subject, comprising:
i) comparing the levels of at least one miR-155 gene product and at least one miR-140 gene product in a subject sample to control; and
ii) diagnosing acute megakaryoblastic leukemia in the event at least one miR-155 gene product and at least one miR-140 gene product levels are lower in the sample compared to control.
12. The method of claim 11 , wherein the control is the level of the at least one miR-155 gene product from a subject that does not have a acute megakaryoblastic leukemia disorder.
13. The method of claim 11 , wherein the subject is a human.
14. The method of claim 11 , wherein the control is the level of the at least one miR-155 gene product from a reference sample comprising non-differentiating megakaryocyte progeny and/or megakaryocytes.
15. The method of claim 11 , which further comprises:
i) comparing the level of at least one additional miR gene product in a subject sample to control, wherein the at least one additional miR gene product is selected from the group consisting of: miR-101; miR-126; miR-99a; miR-99-prec; miR-106; miR-339; miR-99b; miR-149; miR-33; miR-135; and miR-20; and
ii) diagnosing acute megakaryoblastic leukemia in the event that the at least one miR gene product level is higher in the sample compared to control.