Evidence map›Paper›PMID 3474646›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America1987

Amplification and rearrangement of the Kirsten ras oncogene in virus-transformed BALB/c 3T3 cells during malignant tumor progression.

R Radinsky, P M Kraemer, M A Raines, H J Kung, L A Culp

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 1987. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

18 citing papers in PubMed, 57 citations in OpenAlex.

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  12. Interferons alpha and beta down-regulate the expression of basic fibroblast growth factor in human carcinomas.Proceedings of the National Academy of Sciences of the United States of America · 1995
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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 3 institutions in 1 country.

R Radinsky
P M Kraemer
M A Raines
H J Kung
L A Culp
Case Western Reserve University · USLos Alamos National Laboratory · USUniversity School · US

Funding

FIBRONECTIN--PROTEOGLYCAN BINDING IN ADHESION SITESR01CA027755 · NCI · CASE WESTERN RESERVE UNIVERSITY · PI CULP, LLOYD A · 1985 to 1993
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ONCOGENE AND ACTIVATOR: TUMORIGENESIS BY CLONED DNAR01CA038659 · NCI · CASE WESTERN RESERVE UNIVERSITY · PI KUNG, HSING-JIEN · 1985 to 1987
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NCI NIH HHS CA 27755NCI NIH HHS CA 38659
6 · The paper itself

Abstract

Analyses of the cellular and viral Kirsten ras genes (c-Ki-ras and v-Ki-ras, respectively) during malignant tumor progression were performed by using Kirsten murine sarcoma virus-transformed BALB/c 3T3 cells that harbor a replication-defective provirus. After injection into athymic nude mice by four different routes, primary tumors and secondary lung metastases were isolated, adapted to in vitro growth, and analyzed for DNA levels and mRNA expression of both genes for comparison with the originally injected transformed cells and untransformed 3T3 cells. For all tumors (primary or secondary), the v-Ki-ras gene was amplified and v-Ki-ras mRNA expression was highly elevated above that observed in the original transformed cell population. In two of five lung metastases from the i.v. and footpad injection routes, rearranged Ki-ras DNA sequences were observed. Micrometastases from the s.c. route of injection did not display these alterations. Injection of footpad lung tumor cells with rearrangements into a second group of animals led to multiple lung metastases with even further rearrangements correlating with more effective lung colonization/growth ability (overt lung tumors in five of eight animals less than 20 days after injection). However, reinjection of an i.v. lung tumor with rearranged Ki-ras led to no further rearrangements in the lung microfoci tumors isolated greater than 40 days after injection. These data suggest (i) the significance of amplification and elevated expression of v-Ki-ras in tumor formation, (ii) correlation of this amplification with more effective tumor progression, and (iii) the selective advantage that cells with Ki-ras DNA sequence additions have in the formation of overt lung tumors.

Indexed as

Gene AmplificationOncogenesAnimalsCell LineCell Transformation, NeoplasticCell Transformation, ViralDNA, NeoplasmGenotypeLung NeoplasmsMiceMice, Inbred BALB CMice, NudeNeoplasms, ExperimentalProto-OncogenesRNA, MessengerRNA, ViralDNA, NeoplasmRNA, MessengerRNA, Viral

Identifiers

PMID3474646
PMCPMC298810
OpenAlexW1995368256

What OpenQuestion holds

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Read underepoch 390

Registered trials

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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.