Evidence map›Paper›PMID 12637944›Full record

Trial reportCancer gene therapy2003

Assessment of p53 gene transfer and biological activities in a clinical study of adenovirus-p53 gene therapy for recurrent ovarian cancer.

Shu Fen Wen, Vikas Mahavni, Erlinda Quijano, Jeremy Shinoda, Michael Grace, Mary Lynn Musco-Hobkinson, Tong-Yuan Yang, Yuetian Chen, Ingo Runnenbaum, JoAnn Horowitz and 3 more

Abstract readClinical Trial
PubMed Publisher
In one paragraph

Trial report in Cancer gene therapy, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
3.3field-weighted citation impact, top 8% 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

11 citing papers in PubMed, 1 synthesis or guideline pooled it, 46 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Expression of survivin mRNA in gallbladder cancer: a diagnostic and prognostic marker?Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2014
    Article
  6. Clinical antiangiogenic effect of recombinant adenovirus-p53 combined with hyperthermia for advanced cancer.Chinese journal of cancer research = Chung-kuo yen cheng yen chiu · 2013
    Article
  7. Recombinant adenovirus-p53 (Gendicine) sensitizes a pancreatic carcinoma cell line to radiation.Chinese journal of cancer research = Chung-kuo yen cheng yen chiu · 2013
    Article
  8. Article
  9. Article
  10. Article
  11. Intraperitoneal chemotherapy for ovarian cancer.Current oncology reports · 2003
    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

13 authors at 2 institutions in 2 countries.

Shu Fen WenCanji, Inc., San Diego, California 92121, USA. shufen.wen@canji.com
Vikas Mahavni
Erlinda Quijano
Jeremy Shinoda
Michael Grace
Mary Lynn Musco-Hobkinson
Tong-Yuan Yang
Yuetian Chen
Ingo Runnenbaum
JoAnn Horowitz
Dan Maneval
Beth Hutchins
Richard Buller
University of Iowa Hospitals and Clinics · USUniversitäts Frauenklinik · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A cohort study was designed to evaluate the efficiency of gene transfer and whether biological activity from the expressed therapeutic gene resulted after administration of a recombinant adenovirus containing the human wild-type p53 (p53(wt)) gene (rAd-p53 SCH 58500). The cohort study was conducted in five trial subjects with recurrent ovarian cancer. Each trial subject received multiple cycles of rAd-p53 SCH 58500, each cycle comprised of doses of 7.5 x 10(13) particles on each of five consecutive days. Subjects were treated with rAd-p53 SCH 58500 alone during Cycle 1 and in combination with gemcitabine during the subsequent cycles. Both tumor biopsies and peritoneal aspirates were collected and evaluated for gene transfer and evidence of the biological activities of the expressed p53(wt) gene. Using quantitative PCR and RT-PCR, and in situ PCR, gene transfer and expression were documented in tumor biopsies (four of five patients) collected from Cycle 1. Furthermore, upregulation of p21/WAF1, bax and mdm-2, and downregulation of survivin were observed in these same tumor biopsy samples, suggesting that intraperitoneal administration of rAd-p53 SCH 58500 leads to detectable p53 biological activity in target tumor tissue. In addition, gene transfer and its expression were observed in cells obtained from peritoneal aspirates. These fluids were mainly comprised of polymorphonuclear neutrophils, indicating that successful gene transfer can be achieved by multiple cycle intraperitoneal administration of recombinant adenovirus.

Indexed as

AdenoviridaeApoptosisAscitic FluidBiopsyCohort StudiesCyclin-Dependent Kinase Inhibitor p21CyclinsFemaleGene ExpressionGenes, p53Genetic VectorsHumansNeoplasm Recurrence, LocalOvarian NeoplasmsTumor Suppressor Protein p53VirionCDKN1A protein, humanCyclin-Dependent Kinase Inhibitor p21CyclinsTumor Suppressor Protein p53

Identifiers

PMID12637944
OpenAlexW1994038048

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.