Evidence map›Paper›PMID 2116399›Full record

ArticleJapanese journal of cancer research : Gann1990

Novel non-tumorigenic cell variants showing potentially different susceptibility to v-src-induced metastasis.

T Enomoto, H Ayaki, S Nakamori, Y Enomoto, H Inoue, T Kakunaga

Open access · bronzeAbstract read
In one paragraph

Article in Japanese journal of cancer research : Gann, 1990. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 96% 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

0 citing papers in PubMed, 5 citations in OpenAlex.

No citing paper in PubMed yet.

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 3 institutions in 2 countries.

T EnomotoDepartment of Oncogene Research, Osaka University.
H Ayaki
S Nakamori
Y Enomoto
H Inoue
T Kakunaga
Micro-Precision Technologies (United States) · USOncoGenex Pharmaceuticals (United States) · USThe University of Osaka · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Two non-tumorigenic variant cells were isolated from UV-irradiated Balb/c 3T3 cells on the basis of their different responsiveness in phorbol ester-induced morphological change (rounding formation). They showed marked differences of lung metastatic potentials after intravenous injections of their v-src transformants into nude mice; phorbol ester-resistant variant TR4 cells transformed by v-src were hypermetastatic, whereas v-src transformants of phorbol ester-sensitive variant TR5 cells were not metastatic at all. These different metastatic responses were not observed in v-K-ras-induced transformants of the variants. These non-tumorigenic variant cells may pre-acquire the genetic alteration of certain src-specific and metastasis-associated factors. This system may be useful for genetic analysis of the induction of metastasis.

Indexed as

AnimalsCell Transformation, ViralDrug ResistanceFemaleGenes, rasLung NeoplasmsMiceMice, Inbred BALB COncogene Protein pp60(v-src)Tetradecanoylphorbol AcetateOncogene Protein pp60(v-src)Tetradecanoylphorbol Acetate

Identifiers

PMID2116399
PMCPMC5918072
OpenAlexW2002938477

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.