Evidence map›Paper›PMID 12057902›Full record

ArticleThe American journal of pathology2002

An invasion-independent pathway of blood-borne metastasis: a new murine mammary tumor model.

Takashi Sugino, Takashi Kusakabe, Nobuo Hoshi, Tomiko Yamaguchi, Takanori Kawaguchi, Steve Goodison, Masayuki Sekimata, Yoshimi Homma, Toshimitsu Suzuki

Abstract readComparative Study
In one paragraph

Article in The American journal of pathology, 2002. 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
–field-weighted citation impact
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.

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  16. Tumor cell intravasation.American journal of physiology. Cell physiology · 2016
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors.

Takashi SuginoDepartment of Pathology, School of Medicine, Fukushima Medical University, Fukushima City, Japan. sugino@fmu.ac.jp
Takashi Kusakabe
Nobuo Hoshi
Tomiko Yamaguchi
Takanori Kawaguchi
Steve Goodison
Masayuki Sekimata
Yoshimi Homma
Toshimitsu Suzuki

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

It is generally believed that active invasion by cancer cells is essential to the metastatic process. In this report, we describe a murine mammary tumor (MCH66) model of metastasis that does not require invasion into the vascular wall of both the primary tumor and the target organ, in this case, the lung. The process involves intravasation of tumor nests surrounded by sinusoidal blood vessels, followed by intravascular tumor growth in the lung, without penetration of the vascular wall during the process. Comparative studies using a nonmetastatic MCH66 clone (MCH66C8) and another highly invasive metastatic cell line (MCH416) suggested that high angiogenic activity and sinusoidal remodeling of tumor blood vessels were prerequisites for MCH66 metastasis. Differential cDNA analysis identified several genes that were overexpressed by MCH66, including genes for the angiogenesis factor pleiotrophin, and extracellular matrix-associated molecules that may modulate the microenvironment toward neovascularization. Our analyses suggest that tumor angiogenesis plays a role in the induction of invasion-independent metastasis. This model should prove useful in screening and development of new therapeutic agents for cancer metastasis.

Indexed as

AnimalsCarrier ProteinsCytokinesExtracellular Matrix ProteinsFemaleGelatinasesMammary Neoplasms, ExperimentalMiceMice, Inbred C3HNeoplasm InvasivenessNeoplasm MetastasisNeovascularization, PathologicRNA, MessengerTumor Cells, CulturedCarrier ProteinsCytokinesExtracellular Matrix ProteinsGelatinasespleiotrophinRNA, Messenger

Identifiers

PMID12057902
PMCPMC1850839

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.