Evidence map›Paper›PMID 1867326›Full record

ArticleThe American journal of pathology1991

Cell migration and actin organization in cultured human primary, recurrent cutaneous and metastatic melanoma. Time-lapse and image analysis.

H R Byers, T Etoh, J R Doherty, A J Sober, M C Mihm

Open access · greenAbstract read
In one paragraph

Article in The American journal of pathology, 1991. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
2.8field-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

30 citing papers in PubMed, 106 citations in OpenAlex.

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  17. Epac increases melanoma cell migration by a heparan sulfate-related mechanism.American journal of physiology. Cell physiology · 2009
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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

5 authors at 1 institution in 1 country.

H R ByersDepartment of Pathology, Harvard Medical School, Massachusetts General Hospital, Boston 02129.
T Etoh
J R Doherty
A J Sober
M C Mihm
Massachusetts General Hospital · US

Funding

PATHOLOGY AND MECHANISM OF MELANOMA CELL MIGRATIONR29CA045587 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI BYERS, HUGH R · 1987 to 1991
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NCI NIH HHS R29 CA45587
6 · The paper itself

Abstract

Random cell migration and actin organization in seven human primary, recurrent cutaneous, and metastatic melanoma cell lines were studied by time-lapse video recording and image analysis. The migration of over 800 randomly selected cells from the cell lines were recorded using an inverted microscope with an attached incubator housing. The fraction of cells with random migration rates greater than 10 microns/hour was 8% in an established primary melanoma cell line, 2% and 34% in two recurrent cutaneous melanoma cell lines, and 5%, 30%, 31%, and 60% in four metastatic cell lines. The three metastatic cell lines with significantly higher mean migration rates (P less than 0.001) were derived from lymph node metastases, whereas the fourth metastatic cell line was derived from a visceral metastasis. The cellular morphology and presence of cell nests in the original tissue correlated with in vitro cell morphology and the formation of colonies. The ability of cells to organize actin into stress fibers directly correlated with significantly higher random migration rates and lack of colony formation. Characterization of random migration rates and actin organization of human melanoma cells that are isolated from different stages of tumor progression may lend insight into metastasis.

Indexed as

ActinsCell MovementCulture TechniquesHumansImage Processing, Computer-AssistedMelanomaMicroscopy, Phase-ContrastNeoplasm InvasivenessNeoplasm Recurrence, LocalRandom AllocationSkin NeoplasmsTissue DistributionActins

Identifiers

PMID1867326
PMCPMC1886079
OpenAlexW1556944626

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.