Evidence map›Paper›PMID 21045152›Full record

ArticleCancer research2010

Ki-67 as a molecular target for therapy in an in vitro three-dimensional model for ovarian cancer.

Ramtin Rahmanzadeh, Prakash Rai, Jonathan P Celli, Imran Rizvi, Bettina Baron-Lühr, Johannes Gerdes, Tayyaba Hasan

Open access · bronzeAbstract read
In one paragraph

Article in Cancer research, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
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

36 citing papers in PubMed, 76 citations in OpenAlex.

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  15. Effect of removing Kupffer cells on nanoparticle tumor delivery.Proceedings of the National Academy of Sciences of the United States of America · 2017
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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

7 authors at 4 institutions in 2 countries.

Ramtin RahmanzadehWellman Center for Photomedicine, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts 02114, USA.
Prakash Rai
Jonathan P Celli
Imran Rizvi
Bettina Baron-Lühr
Johannes Gerdes
Tayyaba Hasan
Massachusetts General Hospital · USDartmouth College · USHarvard University · USResearch Center Borstel - Leibniz Lung Center · DE

Funding

Photodestruction of Ovarian Cancer: ErbB3 Targeted Aptamer Nanoparticle ConjugateR01CA119388 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI HASAN, TAYYABA · 2005 to 2009
$2.6M
Targeted Photoactivatable Nanocells to Image and Treat Metastic Ovarian CancerRC1CA146337 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI HASAN, TAYYABA · 2009 to 2010
$971k
NCI NIH HHS 5R01 CA119388-03NCI NIH HHS R01 CA119388NCI NIH HHS RC1 CA146337NCI NIH HHS RC1CA146337
6 · The paper itself

Abstract

Targeting molecular markers and pathways implicated in cancer cell growth is a promising avenue for developing effective therapies. Although the Ki-67 protein (pKi-67) is a key marker associated with aggressively proliferating cancer cells and poor prognosis, its full potential as a therapeutic target has never before been successfully shown. In this regard, its nuclear localization presents a major hurdle because of the need for intracellular and intranuclear delivery of targeting and therapeutic moieties. Using a liposomally encapsulated construct, we show for the first time the specific delivery of a Ki-67-directed antibody and subsequent light-triggered death in the human ovarian cancer cell line OVCAR-5. Photoimmunoconjugate-encapsulating liposomes (PICEL) were constructed from anti-pKi-67 antibodies conjugated to fluorescein 5(6)-isothiocyanate, as a photoactivatable agent, followed by encapsulation in noncationic liposomes. Nucleolar localization of the PICELs was confirmed by confocal imaging. Photodynamic activation with PICELs specifically killed pKi-67-positive cancer cells both in monolayer and in three-dimensional (3D) cultures of OVCAR-5 cells, with the antibody TuBB-9 targeting a physiologically active form of pKi-67 but not with MIB-1, directed to a different epitope. This is the first demonstration of (a) the exploitation of Ki-67 as a molecular target for therapy and (b) specific delivery of an antibody to the nucleolus in monolayer cancer cells and in an in vitro 3D model system. In view of the ubiquity of pKi-67 in proliferating cells in cancer and the specificity of targeting in 3D multicellular acini, these findings are promising and the approach merits further investigation.

Indexed as

Antibodies, MonoclonalAntibody SpecificityCell Culture TechniquesCell Line, TumorCell NucleolusCell ProliferationCell SurvivalEpitopesFemaleFlow CytometryFluorescein-5-isothiocyanateHumansKi-67 AntigenLiposomesMicroscopy, ConfocalOvarian NeoplasmsAntibodies, MonoclonalEpitopesFluorescein-5-isothiocyanateKi-67 AntigenLiposomes

Identifiers

PMID21045152
PMCPMC3057762
OpenAlexW2166667895

What OpenQuestion holds

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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.