Evidence map›Paper›PMID 25566504›Full record

ReviewFrontiers in oncology2014

Emerging understanding of multiscale tumor heterogeneity.

Michael J Gerdes, Anup Sood, Christopher Sevinsky, Andrew D Pris, Maria I Zavodszky, Fiona Ginty

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in oncology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed
3.7field-weighted citation impact, top 6% 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

56 citing papers in PubMed, 118 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Cancer stem cells in meningiomas: novel insights and therapeutic implications.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2025
    Review
  6. Review
  7. Article
  8. Article
  9. Review
  10. Engineering Heterogeneous Tumor Models for Biomedical Applications.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024
    Review
  11. Article
  12. Article
  13. Article
  14. Review
  15. Asymmetric Cell Division and Tumor Heterogeneity.Frontiers in cell and developmental biology · 2022
    Review
  16. Review
  17. Cell reports methods · 2021
    Article
  18. Article
  19. Review
  20. Tumor heterogeneity in muscle-invasive bladder cancer.Translational andrology and urology · 2020
    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

6 authors at 1 institution in 1 country.

Michael J GerdesDiagnostic Imaging and Biomedical Technologies, GE Global Research , Niskayuna, NY , USA.
Anup SoodDiagnostic Imaging and Biomedical Technologies, GE Global Research , Niskayuna, NY , USA.
Christopher SevinskyDiagnostic Imaging and Biomedical Technologies, GE Global Research , Niskayuna, NY , USA.
Andrew D PrisDiagnostic Imaging and Biomedical Technologies, GE Global Research , Niskayuna, NY , USA.
Maria I ZavodszkyDiagnostic Imaging and Biomedical Technologies, GE Global Research , Niskayuna, NY , USA.
Fiona GintyDiagnostic Imaging and Biomedical Technologies, GE Global Research , Niskayuna, NY , USA.
General Electric (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cancer is a multifaceted disease characterized by heterogeneous genetic alterations and cellular metabolism, at the organ, tissue, and cellular level. Key features of cancer heterogeneity are summarized by 10 acquired capabilities, which govern malignant transformation and progression of invasive tumors. The relative contribution of these hallmark features to the disease process varies between cancers. At the DNA and cellular level, germ-line and somatic gene mutations are found across all cancer types, causing abnormal protein production, cell behavior, and growth. The tumor microenvironment and its individual components (immune cells, fibroblasts, collagen, and blood vessels) can also facilitate or restrict tumor growth and metastasis. Oncology research is currently in the midst of a tremendous surge of comprehension of these disease mechanisms. This will lead not only to novel drug targets but also to new challenges in drug discovery. Integrated, multi-omic, multiplexed technologies are essential tools in the quest to understand all of the various cellular changes involved in tumorigenesis. This review examines features of cancer heterogeneity and discusses how multiplexed technologies can facilitate a more comprehensive understanding of these features.

Indexed as

cancerheterogeneitymulti-omic analysismultiplexingnext-generation sequencingtumor mechanismstumor microenvironment

Identifiers

PMID25566504
PMCPMC4270176
OpenAlexW2090114571

What OpenQuestion holds

Textmetadata
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.