Evidence map›Paper›PMID 27105489›Full record

ArticleOncotarget2016

Colorectal cancer cells display chaperone dependency for the unconventional prefoldin URI1.

Kamil Andrzej Lipinski, Christian Britschgi, Karen Schrader, Yann Christinat, Lukas Frischknecht, Wilhelm Krek

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.4field-weighted citation impact, top 18% 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

12 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. siRNA-based strategies to combat drug resistance in gastric cancer.Medical oncology (Northwood, London, England) · 2024
    Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Role of RP11-83J16.1, a novel long non-coding RNA, in rheumatoid arthritis.American journal of translational research · 2020
    Article
  8. Review
  9. Article
  10. Article
  11. Review
  12. 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 1 institution in 1 country.

Kamil Andrzej LipinskiInstitute of Molecular Health Sciences, ETH Zurich, 8093 Zurich, Switzerland.
Christian BritschgiInstitute of Molecular Health Sciences, ETH Zurich, 8093 Zurich, Switzerland.
Karen SchraderInstitute of Molecular Health Sciences, ETH Zurich, 8093 Zurich, Switzerland.
Yann ChristinatInstitute of Molecular Health Sciences, ETH Zurich, 8093 Zurich, Switzerland.
Lukas FrischknechtInstitute of Molecular Health Sciences, ETH Zurich, 8093 Zurich, Switzerland.
Wilhelm KrekInstitute of Molecular Health Sciences, ETH Zurich, 8093 Zurich, Switzerland.
ETH Zurich · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chaperone dependency of cancer cells is an emerging trait that relates to the need of transformed cells to cope with the various stresses associated with the malignant state. URI1 (unconventional prefoldin RPB5 interactor 1) encodes a member of the prefoldin (PFD) family of molecular chaperones that acts as part of a heterohexameric PFD complex, the URI1 complex (URI1C), to promote assembly of multiprotein complexes involved in cell signaling and transcription processes. Here, we report that human colorectal cancer (CRCs) cell lines demonstrate differential dependency on URI1 and on the URI1 partner PFD STAP1 for survival, suggesting that this differential vulnerability of CRC cells is directly linked to URI1C chaperone function. Interestingly, in URI1-dependent CRC cells, URI1 deficiency is associated with non-genotoxic p53 activation and p53-dependent apoptosis. URI1-independent CRC cells do not exhibit such effects even in the context of wildtype p53. Lastly, in tumor xenografts, the conditional depletion of URI1 in URI1-dependent CRC cells was, after tumor establishment, associated with severe inhibition of subsequent tumor growth and activation of p53 target genes. Thus, a subset of CRC cells has acquired a dependency on the URI1 chaperone system for survival, providing an example of 'non-oncogene addiction' and vulnerability for therapeutic targeting.

Indexed as

AnimalsApoptosisCell Line, TumorCell SurvivalColorectal NeoplasmsHeterograftsHumansIntracellular Signaling Peptides and ProteinsMiceMolecular ChaperonesRepressor ProteinsTumor Suppressor Protein p53Intracellular Signaling Peptides and ProteinsMolecular ChaperonesRepressor ProteinsTumor Suppressor Protein p53URI1 protein, humanchaperone dependencycolorectal cancerp53prefoldinURI1

Identifiers

PMID27105489
PMCPMC5045422
OpenAlexW2342232857

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.