Evidence map›Paper›PMID 20574452›Full record

ArticleLeukemia2010

Disruption of HOX activity leads to cell death that can be enhanced by the interference of iron uptake in malignant B cells.

T R Daniels, I I Neacato, J A Rodríguez, H S Pandha, R Morgan, M L Penichet

Open access · greenAbstract read
In one paragraph

Article in Leukemia, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

15 citing papers in PubMed, 33 citations in OpenAlex.

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  15. HOX genes in ovarian cancer.Journal of ovarian research · 2011
    Article
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 2 institutions in 2 countries.

T R DanielsDivision of Surgical Oncology, Department of Surgery, David Geffen School of Medicine, University of California, Los Angeles, CA 90095-1782, USA.
I I Neacato
J A Rodríguez
H S Pandha
R Morgan
M L Penichet
University of California, Los Angeles · USUniversity of Surrey · GB

Funding

Women's CancersP30CA016042 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI Samuel Wheeler French · 1985 to 2026
$134.5M
Virology CoreP30AI028697 · NIAID · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI CHEN, IRVIN S.Y. · 1991 to 2018
$39.9M
UCLA Tumor Immunology Training ProgramT32CA009120 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI Steven M. Dubinett, MICHAEL A TEITELL · 1985 to 2026
$10.3M
IMMUNE DYSFUNCTION AND AIDS-ASSOCIATED B-CELL LYMPHOMAR01CA057152 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI MARTINEZ-MAZA, OTONIEL · 1992 to 2009
$2.7M
Anti-TfR IgG3-Av: A New Drug Against Multiple MyelomaR01CA107023 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI PENICHET, MANUEL L · 2005 to 2009
$1.7M
Antibody-mediated Gene Therapy for the Treatment of CancerK01CA138559 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI DANIELS-WELLS, TRACY RUTH · 2009 to 2013
$704k
Cancer Research UK C7822/A3832Howard Hughes Medical InstituteNCI NIH HHS CA-16042NCI NIH HHS K01 CA138559NCI NIH HHS K01CA138559NCI NIH HHS P30 CA016042NCI NIH HHS R01 CA057152NCI NIH HHS R01 CA107023NCI NIH HHS R01CA107023NCI NIH HHS R01CA57152-13S1NCI NIH HHS T32 CA009120NCI NIH HHS T32-CA009120NIAID NIH HHS AI-28697NIAID NIH HHS P30 AI028697
6 · The paper itself

Abstract

The HOX genes encode a family of transcription factors that are dysregulated in several malignancies and have been implicated in oncogenesis and cancer cell survival. Disruption of HOX protein function using the peptide HXR9 has shown anti-tumor effects against melanoma, lung cancer and renal cancer. In this report, we evaluated the expression of all 39 HOX genes in a panel of six malignant B-cell lines, including multiple myeloma cells and found different levels of expression of HOX family members suggesting that they also have a role in malignant B-cell survival. We show that disrupting HOX function using the peptide HXR9 induces significant cytotoxicity in the entire panel of cell lines. Importantly, we found that the cytotoxic effects of HXR9 can be enhanced by combining it with ch128.1Av, an antibody-avidin fusion protein specific for the human transferrin receptor 1 (CD71). Iron starvation induced by the fusion protein contributes to the enhanced effect and involves, at least in part, the induction of a caspase-independent pathway. These results show the relevance of HOX proteins in malignant B-cell survival and suggest that our therapeutic strategy may be effective in the treatment of incurable B-cell malignancies such as multiple myeloma.

Indexed as

Genes, HomeoboxCell DeathCell Line, TumorCell ProliferationHumansIronLymphoma, B-CellPolymerase Chain ReactionIron

Identifiers

PMID20574452
PMCPMC3743965
OpenAlexW1986057540

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.