Evidence map›Paper›PMID 19468267›Full record

ReviewCurrent opinion in hematology2009

Advancements in the molecular pathogenesis of myelodysplastic syndrome.

Pearlie K Epling-Burnette, Alan F List

Abstract readReview
PubMed Publisher
In one paragraph

Review in Current opinion in hematology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

15 citing papers in PubMed, 41 citations in OpenAlex.

  1. Article
  2. Article
  3. Kynurenines as a Novel Target for the Treatment of Malignancies.Pharmaceuticals (Basel, Switzerland) · 2021
    Review
  4. Review
  5. Article
  6. Article
  7. Bone Marrow Immunity and Myelodysplasia.Frontiers in oncology · 2016
    Review
  8. Biology of BM failure syndromes: role of microenvironment and niches.Hematology. American Society of Hematology. Education Program · 2014
    Review
  9. Article
  10. Article
  11. Review
  12. Combination strategies in myelodysplastic syndromes.International journal of hematology · 2012
    Review
  13. Review
  14. Review
  15. Myelodysplastic syndromes: an update on molecular pathology.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2010
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

2 authors at 1 institution in 1 country.

Pearlie K Epling-BurnetteH. Lee Moffitt Cancer Center Immunology Program, Tampa, Florida 33612, USA. Pearlie.Burnette@moffitt.org
Alan F List
Moffitt Cancer Center · US

Funding

Modulation of T cell Homeostasis in Myelodysplastic Syndrome (MDS)R01CA129952 · NCI · H. LEE MOFFITT CANCER CTR & RES INST · PI BURNETTE, PEARLIE K, PINILLA, JAVIER · 2008 to 2012
$2.1M
TARGETED DRUG THERAPY FOR LGL LEUKEMIAR01CA112112 · NCI · H. LEE MOFFITT CANCER CTR &RES INST · PI BURNETTE, PEARLIE K · 2005 to 2008
$1.2M
CSRD VA I01 CX000114NCI NIH HHS R01 CA112112NCI NIH HHS R01CA11211201NCI NIH HHS R01 CA129952
6 · The paper itself

Abstract

purpose of reviewMyelodysplastic syndrome is an important hematological malignancy affecting the expanding aged population. Our understanding of the biology of this disease has been limited by the heterogeneous clinicopathological features, difficulty in creating animal models, and paucity of evidence linking molecular abnormalities to disease pathogenesis. The importance of new advances in myelodysplastic syndrome will be discussed in this review. RECENT

findingsHeightened awareness of the myelodysplastic syndrome burden has garnered rising interest in the development of new treatment strategies and investigation of the molecular basis of this complex disease. A multistep process explains the heterogeneity observed in myelodysplastic syndrome better than a single event, whereby multiple biological forces culminate in telomere erosion and genomic instability. Intrinsic genetic factors within myeloid progenitors along with extrinsic factors in the microenvironment may foster clonal selection. Specific targeted intervention at critical stages along this multistep pathway, prior to acute myeloid leukemia transformation, may produce the best clinical outcome. SUMMARY: Newly identified molecular defects, the creation of animal models, and several advancements in our understanding of the molecular pathogenesis have dramatically improved diagnostic and therapeutic potential of myelodysplastic syndrome.

Indexed as

AnimalsDisease ProgressionHumansMyelodysplastic Syndromes

Identifiers

PMID19468267
OpenAlexW2123923539

What OpenQuestion holds

Textmetadata
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.