Evidence map›Paper›PMID 31126146›Full record

ReviewCells2019

c-Cbl: An Important Regulator and a Target in Angiogenesis and Tumorigenesis.

Chimera L Lyle, Mostafa Belghasem, Vipul C Chitalia

Open access · goldAbstract readReview
In one paragraph

Review in Cells, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
3.0field-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

36 citing papers in PubMed, 57 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. New insights into the role of ubiquitination in angiogenesis (Review).International journal of molecular medicine · 2025
    Review
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. The role of tensins in malignant neoplasms.Archives of medical science : AMS · 2023
    Article
  16. [CBL inhibits proliferation and invasion of breast cancer cells by ubiquitylation-mediated degradation of NCK2].Nan fang yi ke da xue xue bao = Journal of Southern Medical University · 2022
    Article
  17. Article
  18. Review
  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

3 authors at 1 institution in 1 country.

Chimera L LyleDepartment of Medicine, Boston University Medical Center, Boston, MA 02118, USA. clyle@bu.edu.
Mostafa BelghasemDepartment of Pathology and Laboratory Medicine, Boston University Medical Center, Boston, MA 02118, USA. mbelgha@bu.edu.ORCID 0000-0002-2097-6882
Vipul C ChitaliaDepartment of Medicine, Boston University Medical Center, Boston, MA 02118, USA. vichital@bu.edu.
Boston University · US

Funding

RESEARCH TRAINING IN NEPHROLOGYT32DK007053 · NIDDK · BOSTON UNIVERSITY MEDICAL CAMPUS · PI RIFKIN, IAN R · 1986 to 2019
$3.9M
Role of c-Cbl in Colon cancerR01CA175382 · NCI · BOSTON MEDICAL CENTER · PI CHITALIA, VIPUL C · 2014 to 2018
$1.8M
Thrombotic complication of uremia: role of prothrombotic uremic solutesR01HL132325 · NHLBI · BOSTON MEDICAL CENTER · PI CHITALIA, VIPUL C · 2016 to 2019
$1.7M
NCI NIH HHS R01 CA175382NHLBI NIH HHS R01 HL132325NIDDK NIH HHS T32 DK007053
6 · The paper itself

Abstract

Casitas B lineage lymphoma (c-Cbl) is a multifunctional protein with a ubiquitin E3 ligase activity capable of degrading diverse sets of proteins. Although previous work had focused mainly on c-Cbl mutations in humans with hematological malignancies, recent emerging evidence suggests a critical role of c-Cbl in angiogenesis and human solid organ tumors. The combination of its unique structure, modular function, and ability to channelize cues from a rich network of signaling cascades, empowers c-Cbl to assume a central role in these disease models. This review consolidates the structural and functional insights based on recent studies that highlight c-Cbl as a target with tantalizing therapeutic potential in various models of angiogenesis and tumorigenesis.

Indexed as

Animalsbeta CateninCarcinogenesisHumansMiceMolecular Targeted TherapyNeovascularization, PathologicPhospholipase C gammaProto-Oncogene Proteins c-cblUbiquitinationVascular Endothelial Growth Factor AVascular Endothelial Growth Factor Receptor-2Wnt Signaling Pathwaybeta CateninCBL protein, humanCTNNB1 protein, humanKDR protein, humanPhospholipase C gammaPLCG1 protein, humanProto-Oncogene Proteins c-cblVascular Endothelial Growth Factor AVascular Endothelial Growth Factor Receptor-2VEGFA protein, humanangiogenesisc-Cblc-MetEGFRFGFRnon-RTKPDGFRPLCγ1proteasomal degradationRTKtumorsubiquitinationVEGFRWnt signalingβ–catenin

Identifiers

PMID31126146
PMCPMC6563115
OpenAlexW2945795979

What Socratic 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 Socratic graph.