Evidence map›Paper›PMID 18719383›Full record

ArticleCell cycle (Georgetown, Tex.)2008

Mitochondrially targeted wild-type p53 induces apoptosis in a solid human tumor xenograft model.

Gustavo Palacios, Howard C Crawford, Angelina Vaseva, Ute M Moll

Open access · bronzeAbstract read
In one paragraph

Article in Cell cycle (Georgetown, Tex.), 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

10 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
  2. Article
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  4. Article
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  7. Article
  8. Article
  9. The mitochondrial p53 pathway.Biochimica et biophysica acta · 2009
    Review
  10. Review
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

4 authors at 2 institutions in 2 countries.

Gustavo PalaciosDepartment of Pathology, Stony Brook University, Stony Brook, New York 11794, USA.
Howard C Crawford
Angelina Vaseva
Ute M Moll
Stony Brook University · USUniversity of Göttingen · DE

Funding

The in vivo role of the mitochondrial p53 cell death programR01CA060664 · NCI · STATE UNIVERSITY NEW YORK STONY BROOK · PI MOLL, UTE MARTHA · 1999 to 2013
$3.1M
NCI NIH HHS R01 CA060664
6 · The paper itself

Abstract

Classic but also novel roles of p53 are becoming increasingly well characterized. We previously showed that ex vivo retroviral transfer of mitochondrially targeted wild type p53 (mitop53) in the Emu-myc mouse lymphoma model efficiently induces tumor cell killing in vivo. In an effort to further explore the therapeutic potential of mitop53 for its pro-apoptotic effect in solid tumors, we generated replication-deficient recombinant human Adenovirus type 5 vectors. We show here that adenoviral delivery of mitop53 by intratumoral injection into HCT116 human colon carcinoma xenograft tumors in nude mice is surprisingly effective, resulting in tumor cell death of comparable potency to conventional p53. These apoptotic effects in vivo were confirmed by Ad5-mitop53 mediated cell death of HCT116 cells in culture. Together, these data provide encouragement to further explore the potential for novel mitop53 proteins in cancer therapy to execute the shortest known circuitry of p53 death signaling.

Indexed as

ApoptosisAdenoviridaeAnimalsCell Line, TumorColonic NeoplasmsGenetic TherapyGene Transfer TechniquesHumansMiceMice, NudeMitochondriaTumor Suppressor Protein p53Xenograft Model Antitumor AssaysTumor Suppressor Protein p53

Identifiers

PMID18719383
PMCPMC3873818
OpenAlexW2058492795

What OpenQuestion holds

Textmetadata
LicenceTDM
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.