Evidence map›Paper›PMID 16464504›Full record

ReviewPharmacology & therapeutics2006

mda-7/IL-24: multifunctional cancer-specific apoptosis-inducing cytokine.

Pankaj Gupta, Zao-zhong Su, Irina V Lebedeva, Devanand Sarkar, Moira Sauane, Luni Emdad, Michael A Bachelor, Steven Grant, David T Curiel, Paul Dent and 1 more

Open access · greenAbstract readReview
In one paragraph

Review in Pharmacology & therapeutics, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 88 papers.

0numbers the graph read from it
0cells of the map it votes in
88citing papers in PubMed
11.2field-weighted citation impact, top 1% 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

88 citing papers in PubMed, 178 citations in OpenAlex.

  1. Article
  2. Review
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  8. Article
  9. Oncolyic Virotherapy for Prostate Cancer: Lighting a Fire in Winter.International journal of molecular sciences · 2022
    Review
  10. The past, present, and future of immunotherapy for bladder tumors.Medical oncology (Northwood, London, England) · 2022
    Review
  11. Article
  12. Review
  13. Article
  14. Article
  15. Review
  16. Article
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  20. Article

28 more citing papers are in PubMed but not listed here.

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

11 authors at 3 institutions in 1 country.

Pankaj GuptaDepartment of Pathology, Herbert Irving Comprehensive Cancer Center, Columbia University Medical Center, College of Physicians and Surgeons, 630 West 168th Street, New York, NY 10032, United States.
Zao-zhong Su
Irina V Lebedeva
Devanand Sarkar
Moira Sauane
Luni Emdad
Michael A Bachelor
Steven Grant
David T Curiel
Paul Dent
Paul B Fisher
Columbia University Irving Medical Center · USVirginia Commonwealth University · USUniversity of Alabama at Birmingham · US

Funding

Translational Applications of mda-7/IL-24 in CancerP01CA104177 · NCI · VIRGINIA COMMONWEALTH UNIVERSITY · PI FISHER, PAUL B · 2005 to 2009
$6.5M
RADIOSENSITIZATION OF MALIGNANT GLIOMAS BY VIRAL TRANSDUCTION WITH WILD-TYPE P53P01CA072955 · NCI · VIRGINIA COMMONWEALTH UNIVERSITY · PI VALERIE, KRISTOFFER CARL · 1998 to 2007
$6.0M
SIGNALING PATHWAYS REGULATING EPITHELIAL CELL SURVIVALR01DK052825 · NIDDK · VIRGINIA COMMONWEALTH UNIVERSITY · PI DENT, PAUL · 1999 to 2013
$3.3M
MDA-7: Novel Cancer Therapeutic GeneR01CA097318 · NCI · VIRGINIA COMMONWEALTH UNIVERSITY · PI FISHER, PAUL B · 2002 to 2012
$2.8M
Enhanced CRAd for Pancreatic CancerR01CA094084 · NCI · UNIVERSITY OF MINNESOTA · PI YAMAMOTO, MASATO · 2002 to 2013
$2.7M
NF-kappaB Inhibitors and Differentiation-Inducers in LeukemiaR01CA093738 · NCI · VIRGINIA COMMONWEALTH UNIVERSITY · PI GRANT, STEVEN · 2002 to 2011
$2.4M
Interplay between tumor and microenvironment in bone metastasisR01CA259599 · NCI · VIRGINIA COMMONWEALTH UNIVERSITY · PI FISHER, PAUL B, WANG, XIANG-YANG SHAWN · 2021 to 2025
$2.3M
Checkpoint Abrogation and MEK 1/2 Inhibition in MyelomaR01CA100866 · NCI · VIRGINIA COMMONWEALTH UNIVERSITY · PI GRANT, STEVEN · 2003 to 2013
$2.2M
Promotion of Nucleoside Analog Induced Apoptosis by HDIsR01CA063753 · NCI · VIRGINIA COMMONWEALTH UNIVERSITY · PI GRANT, STEVEN · 1994 to 2008
$2.2M
REPLICATIVE ADENOVIRUSES WITH ENHANCED INFECTIVITYR01CA083821 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI CURIEL, DAVID TERRY · 2000 to 2008
$1.9M
PROGRESSION OF THE TRANSFORMED PHENOTYPER01CA035675 · NCI · VIRGINIA COMMONWEALTH UNIVERSITY · PI FISHER, PAUL B · 1985 to 2007
$1.9M
Novel Approaches for Pancreatic Cancer TherapyR01CA098712 · NCI · VIRGINIA COMMONWEALTH UNIVERSITY · PI FISHER, PAUL B · 2003 to 2007
$1.8M
NCI NIH HHS CA083821NCI NIH HHS CA094084NCI NIH HHS CA097318NCI NIH HHS CA098712NCI NIH HHS CA100866NCI NIH HHS CA108520NCI NIH HHS CA111569NCI NIH HHS CA35675NCI NIH HHS CA63753NCI NIH HHS CA72955NCI NIH HHS CA88906NCI NIH HHS CA93738NCI NIH HHS CA93796NCI NIH HHS P01 CA072955NCI NIH HHS P01 CA104177NCI NIH HHS R01 CA035675NCI NIH HHS R01 CA063753NCI NIH HHS R01 CA083821NCI NIH HHS R01 CA088906NCI NIH HHS R01 CA093738NCI NIH HHS R01 CA093796NCI NIH HHS R01 CA094084NCI NIH HHS R01 CA097318NCI NIH HHS R01 CA098712NCI NIH HHS R01 CA100866NCI NIH HHS R01 CA108520NCI NIH HHS R01 CA111569NCI NIH HHS R01 CA259599NCI NIH HHS R56 CA094084NIDDK NIH HHS DK52825NIDDK NIH HHS R01 DK052825
6 · The paper itself

Abstract

"Differentiation therapy" provides a unique and potentially effective, less toxic treatment paradigm for cancer. Moreover, combining "differentiation therapy" with molecular approaches presents an unparalleled opportunity to identify and clone genes mediating cancer growth control, differentiation, senescence, and programmed cell death (apoptosis). Subtraction hybridization applied to human melanoma cells induced to terminally differentiate by treatment with fibroblast interferon (IFN-beta) plus mezerein (MEZ) permitted cloning of melanoma differentiation associated (mda) genes. Founded on its novel properties, one particular mda gene, mda-7, now classified as a member of the interleukin (IL)-10 gene family (IL-24) because of conserved structure, chromosomal location, and cytokine-like properties has become the focus of attention of multiple laboratories. When administered by transfection or adenovirus-transduction into a spectrum of tumor cell types, melanoma differentiation associated gene-7/interleukin-24 (mda-7/IL-24) induces apoptosis, whereas no toxicity is apparent in normal cells. mda-7/IL-24 displays potent "bystander antitumor" activity and also has the capacity to enhance radiation lethality, to induce immune-regulatory activities, and to inhibit tumor angiogenesis. Based on these remarkable attributes and effective antitumor therapy in animal models, this cytokine has taken the important step of entering the clinic. In a Phase I clinical trial, intratumoral injections of adenovirus-administered mda-7/IL-24 (Ad.mda-7) was safe, elicited tumor-regulatory and immune-activating processes, and provided clinically significant activity. This review highlights our current understanding of the diverse activities and properties of this novel cytokine, with potential to become a prominent gene therapy for cancer.

Indexed as

AdenoviridaeAmino Acid SequenceAngiogenesis InhibitorsAnimalsAntineoplastic AgentsApoptosisbeta CateninCell MovementDNA DamageeIF-2 KinaseHumansInterleukin-24InterleukinsMelanomaMitochondriaMolecular Sequence DataAngiogenesis InhibitorsAntineoplastic Agentsbeta CatenineIF-2 KinaseInterleukin-24Interleukinsp38 Mitogen-Activated Protein KinasesPhosphatidylinositol 3-Kinases

Identifiers

PMID16464504
PMCPMC1781515
OpenAlexW2031900842

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.