Evidence map›Paper›PMID 28733386›Full record

ArticleThe Journal of experimental medicine2017

miR-99 regulates normal and malignant hematopoietic stem cell self-renewal.

Mona Khalaj, Carolien M Woolthuis, Wenhuo Hu, Benjamin H Durham, S Haihua Chu, Sarah Qamar, Scott A Armstrong, Christopher Y Park

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed, 1 pooled it
1.6field-weighted citation impact, top 18% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

42 citing papers in PubMed, 1 synthesis or guideline pooled it, 56 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Review
  5. Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. tRNA mNature communications · 2024
    Article
  12. Review
  13. Article
  14. Review
  15. Aberrant stem cell and developmental programs in pediatric leukemia.Frontiers in cell and developmental biology · 2024
    Review
  16. Article
  17. Review
  18. Article
  19. Review
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 3 institutions in 1 country.

Mona KhalajHuman Oncology and Pathogenesis Program, Memorial Sloan Kettering Cancer Center, New York, NY.
Carolien M WoolthuisHuman Oncology and Pathogenesis Program, Memorial Sloan Kettering Cancer Center, New York, NY.
Wenhuo HuHuman Oncology and Pathogenesis Program, Memorial Sloan Kettering Cancer Center, New York, NY.
Benjamin H DurhamHuman Oncology and Pathogenesis Program, Memorial Sloan Kettering Cancer Center, New York, NY.
S Haihua ChuDepartment of Pediatric Oncology, Dana Farber Cancer Institute, Boston, MA.
Sarah QamarHuman Oncology and Pathogenesis Program, Memorial Sloan Kettering Cancer Center, New York, NY.
Scott A ArmstrongDepartment of Pediatric Oncology, Dana Farber Cancer Institute, Boston, MA.
Christopher Y ParkDepartment of Pathology, New York University School of Medicine, New York, NY.
Memorial Sloan Kettering Cancer Center · USDana-Farber Cancer Institute · USNew York University · US

Funding

Cellular and molecular basis of microRNA-29a Induced Acute Myeloid LeukemiaR01CA164120 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI PARK, CHRISTOPHER Y · 2013 to 2017
$1.8M
NCI NIH HHS R01 CA164120
6 · The paper itself

Abstract

The microRNA-99 (miR-99) family comprises a group of broadly conserved microRNAs that are highly expressed in hematopoietic stem cells (HSCs) and acute myeloid leukemia stem cells (LSCs) compared with their differentiated progeny. Herein, we show that miR-99 regulates self-renewal in both HSCs and LSCs. miR-99 maintains HSC long-term reconstitution activity by inhibiting differentiation and cell cycle entry. Moreover, miR-99 inhibition induced LSC differentiation and depletion in an MLL-AF9-driven mouse model of AML, leading to reduction in leukemia-initiating activity and improved survival in secondary transplants. Confirming miR-99's role in established AML, miR-99 inhibition induced primary AML patient blasts to undergo differentiation. A forward genetic shRNA library screen revealed Hoxa1 as a critical mediator of miR-99 function in HSC maintenance, and this observation was independently confirmed in both HSCs and LSCs. Together, these studies demonstrate the importance of noncoding RNAs in the regulation of HSC and LSC function and identify miR-99 as a critical regulator of stem cell self-renewal.

Indexed as

AnimalsCell CycleCell DifferentiationCell Line, TumorCell Self RenewalHematopoietic Stem CellsHomeobox A1 ProteinHomeodomain ProteinsHumansLeukemia, Myeloid, AcuteMiceMice, Inbred C57BLMicroRNAsRNA, Small InterferingTranscription FactorsHomeobox A1 ProteinHomeodomain ProteinsMicroRNAsMIRN99 microRNA, humanRNA, Small InterferingTranscription Factors

Identifiers

PMID28733386
PMCPMC5551568
OpenAlexW2736971239

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.