Evidence map›Paper›PMID 11696456›Full record

ArticleThe American journal of pathology2001

Thrombospondin-1 gene expression affects survival and tumor spectrum of p53-deficient mice.

J Lawler, W M Miao, M Duquette, N Bouck, R T Bronson, R O Hynes

Open access · bronzeAbstract read
In one paragraph

Article in The American journal of pathology, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

43 citing papers in PubMed, 115 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Advancements inMolecules (Basel, Switzerland) · 2024
    Review
  5. Review
  6. Article
  7. Functions of Thrombospondin-1 in the Tumor Microenvironment.International journal of molecular sciences · 2021
    Review
  8. Article
  9. Review
  10. Intravitreal anti-VEGF agents and cardiovascular risk.Internal and emergency medicine · 2020
    Review
  11. THBS1 (thrombospondin-1).Atlas of genetics and cytogenetics in oncology and haematology · 2020
    Article
  12. Article
  13. Article
  14. Integration of pro- and anti-angiogenic signals by endothelial cells.Journal of cell communication and signaling · 2018
    Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. The circadian clock in cancer development and therapy.Progress in molecular biology and translational science · 2013
    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 4 institutions in 1 country.

J LawlerDepartment of Pathology, Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, Massachusetts 02215, USA. lawler@mbcrr.harvard.edu
W M Miao
M Duquette
N Bouck
R T Bronson
R O Hynes
Beth Israel Deaconess Medical Center · USHoward Hughes Medical Institute · USNorthwestern University · USTufts University · US

Funding

CELL-SURFACE STRUCTURE AND TRANSFORMATIONSR01CA017007 · NCI · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI HYNES, RICHARD O · 1985 to 2005
$2.9M
SWITCHING ON OF ANGIOGENESIS DURING TUMOR PROGRESSIONR01CA064239 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI CRAWFORD, SUSAN E. · 1994 to 2010
$2.6M
FUNCTIONAL CHARACTERIZATION OF PLATELET THROMBOSPONDINR01HL028749 · NHLBI · ST. ELIZABETH'S MEDICAL CENTER OF BOSTON · PI LAWLER, JOHN W · 1985 to 1998
–
NCI NIH HHS CA17007NCI NIH HHS CA64239NCI NIH HHS R01 CA017007NCI NIH HHS R01 CA064239NHLBI NIH HHS HL28749
6 · The paper itself

Abstract

In vitro and in vivo data indicate that thrombospondin-1 (TSP1) inhibits tumor progression in several ways including direct effects on cellular growth and apoptosis in the stromal compartment. To evaluate the importance of TSP1 for the progression of naturally arising tumors in vivo, we have crossed TSP1-deficient mice with p53-deficient mice. In p53-null mice, the absence of TSP1 decreases survival from 160 +/- 52 days to 149 +/- 42 days. A log-rank test comparing survival curves for these two populations yields a two-sided P value of 0.0272. For mice that are heterozygous for the p53-null allele, survival is 500 +/- 103 days in the presence of TSP1 expression, and 426 +/- 125 days in its absence (P = 0.0058). Whereas TSP1 expression did not cause a measurable change in the incidence of the majority of tumor types, a statistically significant (P < or = 0.05) decrease in the incidence of osteosarcomas is observed in the absence of TSP1. To determine more directly if host TSP1 inhibits tumor growth, B16F10 melanoma and F9 testicular teratocarcinoma cells have been implanted in C57BL/6J and 129Sv TSP1-null mice, respectively. The B16F10 tumors grow approximately twice as fast in the TSP1-null background and exhibit an increase in vascular density, a decrease in the rate of tumor cell apoptosis, and an increase in the rate of tumor cell proliferation. Increased tumor growth is also observed in the absence of TSP1 on the 129Sv genetic background. These data indicate that endogenous host TSP1 functions as a modifier or landscaper gene to suppress tumor growth.

Indexed as

AnimalsFemaleGene ExpressionGenotypeLoss of HeterozygosityMaleMelanomaMiceMice, Inbred C57BLMice, KnockoutNeoplasms, ExperimentalNeoplasm TransplantationTeratocarcinomaTesticular NeoplasmsThrombospondin 1Tumor Suppressor Protein p53Thrombospondin 1Tumor Suppressor Protein p53

Identifiers

PMID11696456
PMCPMC1867067
OpenAlexW2134674686

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.