Evidence map›Paper›PMID 9926921›Full record

ArticleOncogene1999

Expression of the focal adhesion protein paxillin in lung cancer and its relation to cell motility.

R Salgia, J L Li, D S Ewaniuk, Y B Wang, M Sattler, W C Chen, W Richards, E Pisick, G I Shapiro, B J Rollins and 3 more

Abstract read
PubMed Publisher
In one paragraph

Article in Oncogene, 1999. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

44 citing papers in PubMed, 89 citations in OpenAlex.

  1. Article
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  13. Article
  14. Expression of Paxillin is Correlated with Clinical Prognosis in Colorectal Cancer Patients.Medical science monitor : international medical journal of experimental and clinical research · 2015
    Article
  15. c-Abl mediated tyrosine phosphorylation of paxillin regulates LPS-induced endothelial dysfunction and lung injury.American journal of physiology. Lung cellular and molecular physiology · 2015
    Article
  16. Expression of paxillin in laryngeal squamous cell carcinoma and its prognostic value.International journal of clinical and experimental pathology · 2015
    Article
  17. Article
  18. Article
  19. Article
  20. 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

13 authors at 2 institutions in 1 country.

R SalgiaDivision of Hematologic Oncology, Dana-Farber Cancer Institute and Harvard Medical School, Boston, Massachusetts 02115, USA.
J L Li
D S Ewaniuk
Y B Wang
M Sattler
W C Chen
W Richards
E Pisick
G I Shapiro
B J Rollins
L B Chen
J D Griffin
D J Sugarbaker
Harvard University · USDana-Farber Cancer Institute · US

Funding

SIGNAL TRANSDUCTION PATHWAYS IN STABLE PHASE CHRONIC MYELOID LEUKEMIA CELLSP01DK050654 · NIDDK · DANA-FARBER CANCER INSTITUTE · PI D'ANDREA, ALAN DAVID · 1996 to 2006
$10.3M
ABNORMALITIES OF MOTILITY OF CML CELLSR29CA075348 · NCI · DANA-FARBER CANCER INSTITUTE · PI SALGIA, RAVI · 1997 to 2001
$235k
NCI NIH HHS CA75348NIDDK NIH HHS DK50654
6 · The paper itself

Abstract

Lung cancer can lead to abnormalities of the actin cytoskeleton structure which may be important in transformation. In this study, we have investigated the expression of the cytoskeletal associated protein paxillin in lung cancer. Paxillin is a 68 kDa focal adhesion protein, with four tandem LIM domains at the C-terminus, involved in growth factor receptor, integrin and oncogenic signaling such as v-src, BCR/ABL, and E6 of the papilloma virus. In non-small cell lung cancer (NSCLC) cell lines, paxillin localized to the focal adhesions. The possible role of paxillin in lung cancer cells was assessed by overexpressing green fluorescence protein (GFP)-paxillin construct in two separate NSCLC cell lines (Calu-1 and H661). Over the course of 48 h, GFP-paxillin consistently caused the cells to become round and to decrease cell motility as compared to normal controls, GFP-N-terminus paxillin, or GFP-LIM transfected cells. Because some lung cancers may be quite aggressive and metastasize quickly, which may be related to the cytoskeleton, we determined the expression of paxillin in NSCLC and small cell lung cancer (SCLC) cell lines and patient tumor tissues. Expression of paxillin in NSCLC and SCLC cell lines were determined by Northern blot and Western blot analysis. The expression of paxillin was consistently low in SCLC cell lines, whereas there was paxillin expression in NSCLC cell lines. There was a variability of expression of paxillin in NSCLC tumor tissue as compared to normal lung tissue. In contrast, by immunohistochemistry, we show that there was no detectable expression of paxillin in 5/5 SCLC patients. This data suggests that absence or low level of paxillin protein expression may cause certain lung cancers, such as SCLC, to be more motile and possibly more aggressive.

Indexed as

Cell Movement3T3 CellsAnimalsCarcinoma, Non-Small-Cell LungCarcinoma, Small CellCell Adhesion MoleculesCytoskeletal ProteinsGene ExpressionHumansLung NeoplasmsMicePaxillinPhosphoproteinsRecombinant Fusion ProteinsTumor Cells, CulturedCell Adhesion MoleculesCytoskeletal ProteinsPaxillinPhosphoproteinsPXN protein, humanPxn protein, mouseRecombinant Fusion Proteins

Identifiers

PMID9926921
OpenAlexW2058843151

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.