Evidence map›Paper›PMID 24214290›Full record

ReviewStem cells (Dayton, Ohio)2014

Concise review: Leukemia stem cells in personalized medicine.

Monica L Guzman, John N Allan

Abstract readReview
In one paragraph

Review in Stem cells (Dayton, Ohio), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
–field-weighted citation impact
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

25 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Review
  5. CD8Leukemia · 2019
    Article
  6. Article
  7. Article
  8. Multiparametric Whole Blood Dissection: A one-shot comprehensive picture of the human hematopoietic system.Cytometry. Part A : the journal of the International Society for Analytical Cytology · 2017
    Article
  9. Article
  10. Review
  11. Minimal residual disease in acute myelogenous leukemia.International journal of laboratory hematology · 2017
    Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Micelle Delivery of Parthenolide to Acute Myeloid Leukemia Cells.Cellular and molecular bioengineering · 2015
    Article
  18. Article
  19. Article
  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

2 authors.

Monica L GuzmanDivision of Hematology/Medical Oncology, Department of Medicine, Weill Medical College of Cornell University, New York, New York, USA.
John N Allan

Funding

PHARMACOLOGICAL MODULATION OF EPIGENETIC CHANTGES IN AMLR01CA102031 · NCI · OHIO STATE UNIVERSITY · PI GUZMAN, MONICA L, MARCUCCI, GUIDO · 2004 to 2017
$3.8M
Biomarkers for predicting response to Hsp90 therapyR01CA172546 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI CHIOSIS, GABRIELA, DUNPHY, MARK P. · 2013 to 2017
$2.9M
Selection of Novel Therapies to Ablate Chemoresistant Myeloid Leukemia Stem CellDP2OD007399 · OD · WEILL MEDICAL COLL OF CORNELL UNIV · PI GUZMAN, MONICA L · 2010 to 2010
$2.5M
A role for elevated autophagy in survival and chemoresistance of leukemia stem ceR21CA158728 · NCI · WEILL MEDICAL COLL OF CORNELL UNIV · PI GUZMAN, MONICA L · 2012 to 2013
$393k
NCI NIH HHS R01 CA102031NCI NIH HHS R01 CA172546NCI NIH HHS R21 CA158728NCI NIH HHS R21 CA158728-01A1NIH HHS 1 DP2 OD007399-01NIH HHS DP2 OD007399
6 · The paper itself

Abstract

Despite increased comprehension of acute myelogenous leukemia (AML) pathogenesis, current treatment strategies have done little to improve upon standard induction chemotherapy to induce long-term remissions. Since the identification of the leukemic stem cell, efforts have been placed on identifying therapeutically actionable pathways that distinguish this increasingly important cellular compartment. With the advent of increased genome sequencing efforts and phenotypic characterization, opportunities for personalized treatment strategies are rapidly emerging. In this review, we highlight recent advances in the understanding of leukemic stem cell biology and their potential for translation into clinically relevant therapeutics. NF-kappa B activation, Bcl-2 expression, oxidative and metabolic state, and epigenetic modifications all bear their own clinical implications. With advancements in genetic, epigenetic, and metabolic profiling, personalized strategies may be feasible in the near future to improve outcomes for AML patients.

Indexed as

AnimalsEpigenesis, GeneticGene Expression Regulation, LeukemicGenome, HumanHumansLeukemia, Myeloid, AcuteNeoplastic Stem CellsNF-kappa BProto-Oncogene Proteins c-bcl-2NF-kappa BProto-Oncogene Proteins c-bcl-2Acute myelogenous leukemiaHematopoietic stem cellsLeukemia stem cellsMolecular targeted therapiesTranslational medicine

Identifiers

PMID24214290
PMCPMC4378904

What OpenQuestion holds

Textmetadata
LicenceTDM
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.