Evidence map›Paper›PMID 22621279›Full record

ArticleBreast cancer research : BCR2012

Die and let live: harnessing BikDD to combat breast cancer stem cells.

Mario Giuliano, Meghana V Trivedi, Rachel Schiff

Abstract read
In one paragraph

Article in Breast cancer research : BCR, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

3 authors.

Mario GiulianoLester and Sue Smith Breast Center at Baylor College of Medicine, Houston, TX 77030, USA. rschiff@bcm.edu
Meghana V Trivedi
Rachel Schiff

Funding

TUMOR SUPPRESSOR GENES IN BREAST CANCER DEVELOPMENTP50CA058183 · NCI · UNIVERSITY OF TEXAS HLTH SCI CTR SAN ANT · PI OSBORNE, C KENT · 1992 to 2012
$30.9M
NCI NIH HHS P50 CA58183
6 · The paper itself

Abstract

One of the possible mechanisms contributing to the intrinsic resistance of cancer stem cells (CSCs) to conventional therapies is the inefficiency of activating the apoptotic machinery. In a recent study by Lang and colleagues, the engineered constitutively active pro-apoptotic protein BikDD, which works by inhibiting multiple Bcl-2 family members, was tested in various preclinical breast cancer models. Delivered to cells via an innovative cancer cell-specific gene-therapy approach, BikDD showed potent activity against CSCs and synergized with lapatinib and paclitaxel treatment. This novel and promising therapy warrants further translation to the clinic.

Indexed as

AnimalsApoptosisApoptosis Regulatory ProteinsBreast NeoplasmsCD24 AntigenFemaleHumansHyaluronan ReceptorsLapatinibMembrane ProteinsMiceMice, Inbred NODMice, SCIDMitochondrial ProteinsNeoplastic Stem CellsPaclitaxelApoptosis Regulatory ProteinsBIK protein, humanCD24 AntigenHyaluronan ReceptorsLapatinibMembrane ProteinsMitochondrial ProteinsPaclitaxelProto-Oncogene Proteins c-bcl-2QuinazolinesRNA, Small Interfering

Identifiers

PMID22621279
PMCPMC3446324

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.