Evidence map›Paper›PMID 9670021›Full record

ArticleThe EMBO journal1998

Invasion of T-lymphoma cells: cooperation between Rho family GTPases and lysophospholipid receptor signaling.

J C Stam, F Michiels, R A van der Kammen, W H Moolenaar, J G Collard

Open access · greenAbstract read
In one paragraph

Article in The EMBO journal, 1998. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 62 papers.

0numbers the graph read from it
0cells of the map it votes in
62citing papers in PubMed
10.0field-weighted citation impact, top 1% 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

62 citing papers in PubMed, 221 citations in OpenAlex.

  1. Review
  2. Article
  3. The Role of Lysophosphatidic Acid in Adult Stem Cells.International journal of stem cells · 2020
    Review
  4. Review
  5. Article
  6. Biological effects of RNAi targeted inhibiting Tiam1 gene expression on cholangiocarcinoma cells.International journal of clinical and experimental pathology · 2015
    Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Effects of lysophospholipids on tumor microenvironment.Cancer microenvironment : official journal of the International Cancer Microenvironment Society · 2011
    Article
  17. Review
  18. Targeting sphingosine-1-phosphate in hematologic malignancies.Anti-cancer agents in medicinal chemistry · 2011
    Review
  19. Article
  20. Article

2 more citing papers are in PubMed but not listed here.

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

5 authors at 1 institution in 1 country.

J C StamDivision of Cell Biology, The Netherlands Cancer Institute, Plesmanlaan 121, 1066 CX Amsterdam, The Netherlands.
F Michiels
R A van der Kammen
W H Moolenaar
J G Collard
The Netherlands Cancer Institute · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Rho-like GTPases orchestrate distinct cytoskeletal changes in response to receptor stimulation. Invasion of T-lymphoma cells into a fibroblast monolayer is induced by Tiam1, an activator of the Rho-like GTPase Rac, and by constitutively active V12Rac1. Here we show that activated V12Cdc42 can also induce invasion of T-lymphoma cells. Activated RhoA potentiates invasion, but fails by itself to mimic Rac and Cdc42. However, invasion is inhibited by the Rho-inactivating C3 transferase. Thus, RhoA is required but not sufficient for invasion. Invasion of T-lymphoma cells is critically dependent on the presence of serum. Serum can be replaced by the serum-borne lipids lysophosphatidic acid (LPA) and sphingosine-1-phosphate (S1P) (10(-7)-10(-6) M), which act on distinct G protein-linked receptors to activate RhoA and phospholipase C (PLC)-Ca2+ signaling. LPA- and S1P-induced invasion is preceded by Rho-dependent F-actin redistribution and pseudopodia formation. However, expression of both V14RhoA and V12Rac1 does not bypass the LPA/S1P requirement for invasion, indicating involvement of an additional signaling pathway independent of RhoA. The PLC inhibitor U-73122, but not the inactive analog U-73343, abolishes invasion. Our results indicate that T-lymphoma invasion is driven by Tiam1/Rac or Cdc42 activation, and is dependent on LPA/S1P receptor-mediated RhoA and PLC signaling pathways which lead to pseudopod formation and enhanced infiltration.

Indexed as

Botulinum ToxinsReceptors, G-Protein-CoupledActinsADP Ribose TransferasesAnimalsBloodCalciumcdc42 GTP-Binding ProteinCell Cycle ProteinsCell LineCell SizeCytoskeletonFibroblastsGTP-Binding ProteinsGTP PhosphohydrolasesGuanine Nucleotide Exchange FactorsActinsADP Ribose TransferasesBotulinum ToxinsCalciumcdc42 GTP-Binding ProteinCell Cycle Proteinsexoenzyme C3, Clostridium botulinumGTP-Binding ProteinsGTP PhosphohydrolasesGuanine Nucleotide Exchange FactorsLysophospholipidsNeoplasm ProteinsProtein Kinase CProteinsrac GTP-Binding ProteinsReceptors, Cell SurfaceReceptors, G-Protein-CoupledReceptors, Lysophosphatidic AcidrhoA GTP-Binding ProteinSphingosinesphingosine 1-phosphateTiam1 protein, ratT-Lymphoma Invasion and Metastasis-inducing Protein 1Type C Phospholipases

Identifiers

PMID9670021
PMCPMC1170739
OpenAlexW2034566357

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.