Evidence map›Paper›PMID 25843776›Full record

ArticleCellular signalling2015

The Bmi-1 helix-turn and ring finger domains are required for Bmi-1 antagonism of (-) epigallocatechin-3-gallate suppression of skin cancer cell survival.

Sivaprakasam Balasubramanian, Tiffany M Scharadin, Bingshe Han, Wen Xu, Richard L Eckert

Erratum issuedOpen access · greenAbstract read
In one paragraph

Article in Cellular signalling, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.1field-weighted citation impact, top 20% 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

6 citing papers in PubMed, 11 citations in OpenAlex.

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  5. Review
  6. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 1 institution in 1 country.

Sivaprakasam BalasubramanianDepartment of Biochemistry and Molecular Biology, University of Maryland School of Medicine, Baltimore, MD, USA.
Tiffany M ScharadinDepartment of Biochemistry and Molecular Biology, University of Maryland School of Medicine, Baltimore, MD, USA.
Bingshe HanDepartment of Biochemistry and Molecular Biology, University of Maryland School of Medicine, Baltimore, MD, USA.
Wen XuDepartment of Biochemistry and Molecular Biology, University of Maryland School of Medicine, Baltimore, MD, USA.
Richard L EckertDepartment of Biochemistry and Molecular Biology, University of Maryland School of Medicine, Baltimore, MD, USA; Department of Dermatology, University of Maryland School of Medicine, Baltimore, MD, USA; Department of Obstetrics and Gynecology, University of Maryland School of Medicine, Baltimore, MD, USA; Department of Greenebaum Cancer Center, University of Maryland School of Medicine, Baltimore, MD, USA. Electronic address: reckert@umaryland.edu.
University of Maryland, Baltimore · US

Funding

Polycomb proteins and skin cancer preventionR01CA131074 · NCI · UNIVERSITY OF MARYLAND BALTIMORE · PI ECKERT, RICHARD L. · 2008 to 2017
$4.6M
Stem Cells and Skin Cancer Prevention and AngiogenesisR01CA184027 · NCI · UNIVERSITY OF MARYLAND BALTIMORE · PI ECKERT, RICHARD L. · 2015 to 2019
$1.9M
AKT pathway as a therapeutic tumor vessel targetR01CA131064 · NCI · BETH ISRAEL DEACONESS MEDICAL CENTER · PI BENJAMIN, LAURA E · 2008 to 2009
$792k
NCI NIH HHS R01 CA131064NCI NIH HHS R01 CA131074NCI NIH HHS R01 CA184027
6 · The paper itself

Abstract

The Bmi-1 Polycomb group (PcG) protein is an important epigenetic regulator of chromatin status. Elevated Bmi-1 expression is observed in skin cancer and contributes to cancer cell survival. (-) Epigallocatechin-3-gallate (EGCG), an important green tea-derived cancer prevention agent, reduces Bmi-1 level resulting in reduced skin cancer cell survival. This is associated with increased p21(Cip1) and p27(Kip1) expression, reduced cyclin, and cyclin dependent kinase expression, and increased cleavage of apoptotic markers. These EGCG-dependent changes are attenuated by vector-mediated maintenance of Bmi-1 expression. In the present study, we identify Bmi-1 functional domains that are required for this response. Bmi-1 expression reverses the EGCG-dependent reduction in SCC-13 cell survival, but Bmi-1 mutants lacking the helix-turn-helix-turn-helix-turn (Bmi-1ΔHT) or ring finger (Bmi-1ΔRF) domains do not reverse the EGCG impact. The reduction in Ring1B ubiquitin ligase activity, observed in the presence of mutant Bmi-1, is associated with reduced ability of these mutants to interact with and activate Ring1B ubiquitin ligase, the major ligase responsible for the ubiquitination of histone H2A during chromatin condensation. This results in less chromatin condensation leading to increased tumor suppressor gene expression and reduced cell survival; thereby making the cells more susceptible to the anti-survival action of EGCG. We further show that these mutants act in a dominant-negative manner to inhibit the action of endogenous Bmi-1. Our results suggest that the HT and RF domains are required for Bmi-1 ability to maintain skin cancer cell survival in response to cancer preventive agents.

Indexed as

Anticarcinogenic AgentsApoptosisCatechinCell Line, TumorCell SurvivalGene Expression RegulationHumansMutationPolycomb-Group ProteinsPolycomb Repressive Complex 1RING Finger DomainsSkin NeoplasmsAnticarcinogenic AgentsBMI1 protein, humanCatechinepigallocatechin gallatePolycomb-Group ProteinsPolycomb Repressive Complex 1RNF2 protein, humanChemopreventionEGCGEzh2Histone methylationPolycomb group proteinsSkin cancer

Identifiers

PMID25843776
PMCPMC4756650
OpenAlexW1970984489

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.