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Sökning: id:"swepub:oai:lup.lub.lu.se:1e308175-c529-4304-8204-aef3eaa3617e" > Analysis of nonleuk...

Analysis of nonleukemic cellular subcompartments reconstructs clonal evolution of acute myeloid leukemia and identifies therapy-resistant preleukemic clones

Saeed, Borhan R. (författare)
Heidelberg University
Manta, Linda (författare)
Heidelberg University
Raffel, Simon (författare)
German Cancer Research Centre,Heidelberg University
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Pyl, Paul Theodor (författare)
Lund University,Lunds universitet,Bröstcancer Proteogenomik,Forskargrupper vid Lunds universitet,LUCC: Lunds universitets cancercentrum,Övriga starka forskningsmiljöer,Breast cancer Proteogenomics,Lund University Research Groups,LUCC: Lund University Cancer Centre,Other Strong Research Environments,European Molecular Biology Laboratory Heidelberg
Buss, Eike C. (författare)
Heidelberg University
Wang, Wenwen (författare)
Fudan University Shanghai Cancer Center (FUSCC),Heidelberg University,Fudan University
Eckstein, Volker (författare)
Heidelberg University
Jauch, Anna (författare)
Heidelberg University
Trumpp, Andreas (författare)
German Cancer Research Centre
Huber, Wolfgang (författare)
European Molecular Biology Laboratory Heidelberg
Ho, Anthony D. (författare)
Heidelberg University
Lutz, Christoph (författare)
Heidelberg University,Praxis für Hämatologie und Onkologie, Koblenz
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 (creator_code:org_t)
2021-01-18
2021
Engelska.
Ingår i: International Journal of Cancer. - : Wiley. - 0020-7136 .- 1097-0215. ; 148:11, s. 2825-2838
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • To acquire a better understanding of clonal evolution of acute myeloid leukemia (AML) and to identify the clone(s) responsible for disease recurrence, we have comparatively studied leukemia-specific mutations by whole-exome-sequencing (WES) of both the leukemia and the nonleukemia compartments derived from the bone marrow of AML patients. The T-lymphocytes, B-lymphocytes and the functionally normal hematopoietic stem cells (HSC), that is, CD34+/CD38−/ALDH+ cells for AML with rare-ALDH+ blasts (<1.9% ALDH+ cells) were defined as the nonleukemia compartments. WES identified 62 point-mutations in the leukemia compartment derived from 12 AML-patients at the time of diagnosis and 73 mutations in 3 matched relapse cases. Most patients (8/12) showed 4 to 6 point-mutations per sample at diagnosis. Other than the mutations in the recurrently mutated genes such as DNMT3A, NRAS and KIT, we were able to identify novel point-mutations that have not yet been described in AML. Some leukemia-specific mutations and cytogenetic abnormalities including DNMT3A(R882H), EZH2(I146T) and inversion(16) were also detectable in the respective T-lymphocytes, B-lymphocytes and HSC in 5/12 patients, suggesting that preleukemia HSC might represent the source of leukemogenesis for these cases. The leukemic evolution was reconstructed for five cases with detectable preleukemia clones, which were tracked in follow-up and relapse samples. Four of the five patients with detectable preleukemic mutations developed relapse. The presence of leukemia-specific mutations in these nonleukemia compartments, especially after chemotherapy or after allogeneic stem cell transplantation, is highly relevant, as these could be responsible for relapse. This discovery may facilitate the identification of novel targets for long-term cure.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Cancer och onkologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cancer and Oncology (hsv//eng)

Nyckelord

acute myeloid leukemia (AML)
clonal evolution
hematopoietic stem cells (HSC)
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