Evidence map›Paper›PMID 24201748›Full record

ArticleBritish journal of cancer2014

Pancreatic stellate cells promote hapto-migration of cancer cells through collagen I-mediated signalling pathway.

J Lu, S Zhou, M Siech, H Habisch, T Seufferlein, M G Bachem

Open access · hybridAbstract read
In one paragraph

Article in British journal of cancer, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
2.8field-weighted citation impact, top 11% 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

39 citing papers in PubMed, 57 citations in OpenAlex.

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  10. Amoeboid migration in health and disease: Immune responsesFrontiers in cell and developmental biology · 2022
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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.

J LuDepartment of Clinical Chemistry, University of Ulm, Albert-Einstein-Allee 23, 89081, Ulm, Germany.
S ZhouDepartment of Clinical Chemistry, University of Ulm, Albert-Einstein-Allee 23, 89081, Ulm, Germany.
M SiechDepartment of General Surgery, Ostalb Hospital, Im Kälblesrain 1, 73430, Aalen, Germany.
H HabischDepartment of Clinical Chemistry, University of Ulm, Albert-Einstein-Allee 23, 89081, Ulm, Germany.
T SeufferleinDepartment of Internal Medicine, University of Ulm, Albert-Einstein-Allee 23, 89081, Ulm, Germany.
M G BachemDepartment of Clinical Chemistry, University of Ulm, Albert-Einstein-Allee 23, 89081, Ulm, Germany.
Universität Ulm · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPancreatic stellate cells (PSCs) promote metastasis as well as local growth of pancreatic cancer. However, the factors mediating the effect of PSCs on pancreatic cancer cells have not been clearly identified.

methodsWe used a modified Boyden chamber assay as an in vitro model to investigate the role of PSCs in migration of Panc1 and UlaPaCa cells and to identify the underlying mechanisms.

resultsPSC supernatant (PSC-SN) dose-dependently induced the trans-migration of Panc1 and UlaPaCa cells, mainly via haptokinesis and haptotaxis, respectively. In contrast to poly-L-lysine or fibronectin, collagen I resembled PSC-SN with respect to its effect on cancer cell behaviours, including polarised morphology, facilitated adhesion, accelerated motility and stimulated trans-migration. Blocking antibodies against integrin α2/β1 subunits significantly attenuated PSC-SN- or collagen I-promoted cell trans-migration and adhesion. Moreover, both PSC-SN and collagen I induced the formation of F-actin and focal adhesions in cells, which was consistent with the constantly enhanced phosphorylation of focal adhesion kinase (FAK, Tyr397). Inhibition of FAK function by an inhibitor or small interference RNAs significantly diminished the effect of PSC-SN or collagen I on haptotaxis/haptokinesis of pancreatic cancer cells.

conclusionCollagen I is the major mediator for PSC-SN-induced haptokinesis of Panc1 and haptotaxis of UlaPaCa by activating FAK signalling via binding to integrin α2β1.

Indexed as

ActinsCell AdhesionCell Line, TumorCell MovementCollagen Type IFocal Adhesion Protein-Tyrosine KinasesHumansLiverPancreatic NeoplasmsPancreatic Stellate CellsPhosphorylationSignal TransductionActinsCollagen Type IFocal Adhesion Protein-Tyrosine Kinases

Identifiers

PMID24201748
PMCPMC3899756
OpenAlexW1991557260

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.