Evidence map›Paper›PMID 22546915›Full record

ArticleComparative medicine2012

A new apparatus and surgical technique for the dual perfusion of human tumor xenografts in situ in nude rats.

Robert T Dauchy, Erin M Dauchy, Lulu Mao, Victoria P Belancio, Steven M Hill, David E Blask

Open access · greenAbstract read
In one paragraph

Article in Comparative medicine, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.8field-weighted citation impact, top 28% 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

6 citing papers in PubMed, 9 citations in OpenAlex.

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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

6 authors at 1 institution in 1 country.

Robert T DauchyDepartment of Structural and Cellular Biology, Tulane University School of Medicine, Tulane, Louisiana, USA. rdauchy@tulane.edu
Erin M Dauchy
Lulu Mao
Victoria P Belancio
Steven M Hill
David E Blask
Tulane University · US

Funding

UNCOVERING THE MECHANISMS OF OSTEOSARCOMA METASTASIS SUPPRESSION BY MTBPP20RR020152 · NCRR · TULANE UNIVERSITY OF LOUISIANA · PI FLEMINGTON, ERIK K · 2004 to 2011
$17.0M
Mentoring a Cancer Genetics ProgramP20GM103518 · NIGMS · TULANE UNIVERSITY OF LOUISIANA · PI DEININGER, PRESCOTT L. · 2012 to 2013
$4.3M
L 1 element as an inrinsic factor of mammalian agingK01AG030074 · NIA · TULANE UNIVERSITY OF LOUISIANA · PI BELANCIO, VICTORIA PEREPELITSA · 2008 to 2012
$504k
NCRR NIH HHS P20 RR020152NCRR NIH HHS P20RR020152NCRR NIH HHS P20RR02020152NIA NIH HHS 5K01AG030074-02NIA NIH HHS K01 AG030074NIGMS NIH HHS P20 GM103518
6 · The paper itself

Abstract

We present a new perfusion system and surgical technique for simultaneous perfusion of 2 tissue-isolated human cancer xenografts in nude rats by using donor blood that preserves a continuous flow. Adult, athymic nude rats (Hsd:RH-Foxn1(rnu)) were implanted with HeLa human cervical or HT29 colon adenocarcinomas and grown as tissue-isolated xenografts. When tumors reached an estimated weight of 5 to 6 g, rats were prepared for perfusion with donor blood and arteriovenous measurements. The surgical procedure required approximately 20 min to complete for each tumor, and tumors were perfused for a period of 150 min. Results showed that tumor venous blood flow, glucose uptake, lactic acid release, O(2) uptake and CO(2) production, uptake of total fatty acid and linoleic acid and conversion to the mitogen 13-HODE, cAMP levels, and activation of several marker kinases were all well within the normal physiologic, metabolic, and signaling parameters characteristic of individually perfused xenografts. This new perfusion system and technique reduced procedure time by more than 50%. These findings demonstrate that 2 human tumors can be perfused simultaneously in situ or ex vivo by using either rodent or human blood and suggest that the system may also be adapted for use in the dual perfusion of other organs. Advantages of this dual perfusion technique include decreased anesthesia time, decreased surgical manipulation, and increased efficiency, thereby potentially reducing the numbers of laboratory animals required for scientific investigations.

Indexed as

PerfusionAdenocarcinomaAnimalsArtificial OrgansBlood GlucoseCarbon DioxideCell ProliferationColonic NeoplasmsCyclic AMPEnzyme ActivationEquipment DesignFatty AcidsFemaleHeLa CellsHemodynamicsHT29 CellsBlood GlucoseCarbon DioxideCyclic AMPFatty AcidsLactic AcidOxygenProtein Kinases

Identifiers

PMID22546915
PMCPMC3318246
OpenAlexW1603347278

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.