Evidence map›Paper›PMID 29379165›Full record

ReviewOncogene2018

MUC1-C activates polycomb repressive complexes and downregulates tumor suppressor genes in human cancer cells.

Hasan Rajabi, Masayuki Hiraki, Donald Kufe

Abstract readReview
In one paragraph

Review in Oncogene, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed
2.1field-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

52 citing papers in PubMed, 71 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
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  7. Article
  8. Research progress of MUC1 in genitourinary cancers.Cellular & molecular biology letters · 2024
    Review
  9. Article
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  11. Article
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  15. Review
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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

3 authors at 2 institutions in 2 countries.

Hasan RajabiDana-Farber Cancer Institute, Harvard Medical School, Boston, MA, USA.
Masayuki HirakiDana-Farber Cancer Institute, Harvard Medical School, Boston, MA, USA.
Donald KufeDana-Farber Cancer Institute, Harvard Medical School, Boston, MA, USA. donald_kufe@dfci.harvard.edu.ORCID 0000-0001-5743-8888
Harvard University · USOsaka Gakuin University · JP

Funding

Targeting the MUC1-C Oncoprotein in Triple-Negative Breast CancerR01CA097098 · NCI · DANA-FARBER CANCER INSTITUTE · PI DONALD W. KUFE · 2002 to 2026
$8.8M
MUC1-C Oncoprotein Evades Immune Destruction in Non-small Cell Lung CancerR01CA166480 · NCI · DANA-FARBER CANCER INST · PI KUFE, DONALD W., WONG, KWOK KIN · 2012 to 2021
$6.3M
Immunotherapeutic Approaches Targeting the MUC1-C Oncoprotein in Triple-Negative Breast CancerR21CA216553 · NCI · DANA-FARBER CANCER INST · PI KUFE, DONALD W. · 2017 to 2018
$377k
NCI NIH HHS R01 CA097098NCI NIH HHS R01 CA166480NCI NIH HHS R21 CA216553
6 · The paper itself

Abstract

The PRC2 and PRC1 complexes are aberrantly expressed in human cancers and have been linked to decreases in patient survival. MUC1-C is an oncoprotein that is also overexpressed in diverse human cancers and is associated with a poor prognosis. Recent studies have supported a previously unreported function for MUC1-C in activating PRC2 and PRC1 in cancer cells. In the regulation of PRC2, MUC1-C (i) drives transcription of the EZH2 gene, (ii) binds directly to EZH2, and (iii) enhances occupancy of EZH2 on target gene promoters with an increase in H3K27 trimethylation. Regarding PRC1, which is recruited to PRC2 sites in the hierarchical model, MUC1-C induces BMI1 transcription, forms a complex with BMI1, and promotes H2A ubiquitylation. MUC1-C thereby contributes to the integration of PRC2 and PRC1-mediated repression of tumor suppressor genes, such as CDH1, CDKN2A, PTEN and BRCA1. Like PRC2 and PRC1, MUC1-C is associated with the epithelial-mesenchymal transition (EMT) program, cancer stem cell (CSC) state, and acquisition of anticancer drug resistance. In concert with these observations, targeting MUC1-C downregulates EZH2 and BMI1, inhibits EMT and the CSC state, and reverses drug resistance. These findings emphasize the significance of MUC1-C as a therapeutic target for inhibiting aberrant PRC function and reprogramming the epigenome in human cancers.

Indexed as

Genes, Tumor SuppressorAnimalsGene Expression Regulation, NeoplasticHumansMucin-1NeoplasmsOncogene ProteinsPolycomb-Group ProteinsPolycomb Repressive Complex 1Polycomb Repressive Complex 2Protein IsoformsMUC1 protein, humanMucin-1Oncogene ProteinsPolycomb-Group ProteinsPolycomb Repressive Complex 1Polycomb Repressive Complex 2Protein Isoforms

Identifiers

PMID29379165
PMCPMC5908737
OpenAlexW2790601065

What OpenQuestion holds

Textmetadata
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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.