Evidence map›Paper›PMID 25496728›Full record

ArticleeLife2014

Tumor evolutionary directed graphs and the history of chronic lymphocytic leukemia.

Jiguang Wang, Hossein Khiabanian, Davide Rossi, Giulia Fabbri, Valter Gattei, Francesco Forconi, Luca Laurenti, Roberto Marasca, Giovanni Del Poeta, Robin Foà and 3 more

Open access · goldAbstract read
In one paragraph

Article in eLife, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
6.3field-weighted citation impact, top 3% 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

27 citing papers in PubMed, 71 citations in OpenAlex.

  1. Article
  2. Onco-Breastomics: An Eco-Evo-Devo Holistic Approach.International journal of molecular sciences · 2024
    Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Chronic Lymphocytic Leukemia.Cold Spring Harbor perspectives in medicine · 2021
    Review
  8. Clonal dynamics in chronic lymphocytic leukemia.Hematology. American Society of Hematology. Education Program · 2019
    Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Review
  18. Clinical Implications of Novel Genomic Discoveries in Chronic Lymphocytic Leukemia.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2017
    Review
  19. Article
  20. Chronic lymphocytic leukaemia.Nature reviews. Disease primers · 2017
    Review
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

13 authors at 9 institutions in 3 countries.

Jiguang WangDepartment of Biomedical Informatics, Columbia University, New York, United States.
Hossein KhiabanianDepartment of Biomedical Informatics, Columbia University, New York, United States.
Davide RossiDivision of Hematology, Department of Translational Medicine, Amedeo Avogadro University of Eastern Piedmont, Novara, Italy.
Giulia FabbriInstitute for Cancer Genetics, Columbia University, New York, United States.
Valter GatteiClinical and Experimental Onco-Hematology Unit, Centro di Riferimento Oncologico, Aviano, Italy.
Francesco ForconiCancer Sciences Unit, Cancer Research UK Centre, University of Southampton, Southampton, United Kingdom.
Luca LaurentiInstitute of Hematology, Catholic University of the Sacred Heart, Rome, Italy.
Roberto MarascaDivision of Hematology, Department of Oncology and Hematology, University of Modena and Reggio Emilia, Modena, Italy.
Giovanni Del PoetaDepartment of Hematology, Tor Vergata University, Rome, Italy.
Robin FoàDepartment of Cellular Biotechnologies and Hematology, Sapienza University, Rome, Italy.
Laura PasqualucciInstitute for Cancer Genetics, Columbia University, New York, United States.
Gianluca GaidanoDivision of Hematology, Department of Translational Medicine, Amedeo Avogadro University of Eastern Piedmont, Novara, Italy.
Raul RabadanDepartment of Biomedical Informatics, Columbia University, New York, United States.
Columbia University · USCancer Genetics (United States) · USUniversità degli Studi del Piemonte Orientale “Amedeo Avogadro” · ITCancer Research UK · GBCentro di Riferimento Oncologico · ITSapienza University of Rome · ITUniversità Cattolica del Sacro Cuore · ITUniversity of Modena and Reggio Emilia · ITUniversity of Rome Tor Vergata · IT

Funding

Nation Center: Multi-Scale Study- Cellular Networks(RMI)U54CA121852 · NCI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI CALIFANO, ANDREA · 2005 to 2015
$37.4M
Clinical and Translational Science AwardUL1TR000040 · NCATS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI GINSBERG, HENRY N · 2012 to 2015
$26.2M
Identification and modeling of driver genetic modules in glioblastomaR01CA179044 · NCI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI IAVARONE, ANTONIO, RABADAN, RAUL · 2014 to 2018
$2.3M
(PQB5) Reconstruction of Evolutionary Networks using Cross-Sectional Genomic DataR01CA185486 · NCI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI LASORELLA, ANNA, RABADAN, RAUL · 2014 to 2017
$2.1M
NCATS NIH HHS UL1 TR000040NCI NIH HHS 1R01CA179044-01A1NCI NIH HHS 1R01CA185486-01NCI NIH HHS 1 U54 CA121852-05NCI NIH HHS R01 CA179044NCI NIH HHS R01 CA185486NCI NIH HHS U54 CA121852
6 · The paper itself

Abstract

Cancer is a clonal evolutionary process, caused by successive accumulation of genetic alterations providing milestones of tumor initiation, progression, dissemination, and/or resistance to certain therapeutic regimes. To unravel these milestones we propose a framework, tumor evolutionary directed graphs (TEDG), which is able to characterize the history of genetic alterations by integrating longitudinal and cross-sectional genomic data. We applied TEDG to a chronic lymphocytic leukemia (CLL) cohort of 70 patients spanning 12 years and show that: (a) the evolution of CLL follows a time-ordered process represented as a global flow in TEDG that proceeds from initiating events to late events; (b) there are two distinct and mutually exclusive evolutionary paths of CLL evolution; (c) higher fitness clones are present in later stages of the disease, indicating a progressive clonal replacement with more aggressive clones. Our results suggest that TEDG may constitute an effective framework to recapitulate the evolutionary history of tumors.

Indexed as

Clonal EvolutionGene FrequencyHumansLeukemia, Lymphocytic, Chronic, B-Cellchronic lymphocytic leukemiaevolutionary biologygenomicshumanhuman biologymedicinenext generation sequencingtumor evolutionary

Identifiers

PMID25496728
PMCPMC4308685
OpenAlexW2148899115

What OpenQuestion holds

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LicenceCC BY
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.