Evidence map›Paper›PMID 26700806›Full record

ArticleNature2016

Targeting PTPRK-RSPO3 colon tumours promotes differentiation and loss of stem-cell function.

Elaine E Storm, Steffen Durinck, Felipe de Sousa e Melo, Jarrod Tremayne, Noelyn Kljavin, Christine Tan, Xiaofen Ye, Cecilia Chiu, Thinh Pham, Jo-Anne Hongo and 8 more

Abstract read
PubMed Publisher
In one paragraph

Article in Nature, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 158 papers.

0numbers the graph read from it
0cells of the map it votes in
158citing papers in PubMed
10.8field-weighted citation impact, top 1% 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

158 citing papers in PubMed, 248 citations in OpenAlex.

  1. Building and regenerating intestines by manipulating intestinal stem cells.Nature reviews. Gastroenterology & hepatology · 2026
    Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Frontiers in cell and developmental biology · 2026
    Article
  7. Article
  8. Review
  9. Article
  10. World journal of gastrointestinal oncology · 2025
    Article
  11. Review
  12. Article
  13. Review
  14. Review
  15. Radiation-induced cellular plasticity primes glioblastoma for forskolin-mediated differentiation.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  16. Article
  17. Article
  18. Review
  19. Review
  20. Review

98 more citing papers are in PubMed but not listed here.

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

18 authors at 1 institution in 1 country.

Elaine E StormMolecular Oncology, Genentech, Inc., 1 DNA Way, South San Francisco, California 94080, USA.
Steffen DurinckMolecular Biology, Genentech, Inc., 1 DNA Way, South San Francisco, California 94080, USA.
Felipe de Sousa e MeloMolecular Oncology, Genentech, Inc., 1 DNA Way, South San Francisco, California 94080, USA.
Jarrod TremayneTranslational Oncology, Genentech, Inc., 1 DNA Way, South San Francisco, California 94080, USA.
Noelyn KljavinMolecular Oncology, Genentech, Inc., 1 DNA Way, South San Francisco, California 94080, USA.
Christine TanAntibody Engineering, Genentech, Inc., 1 DNA Way, South San Francisco, California 94080, USA.
Xiaofen YeDiscovery Oncology, Genentech, Inc., 1 DNA Way, South San Francisco, California 94080, USA.
Cecilia ChiuAntibody Engineering, Genentech, Inc., 1 DNA Way, South San Francisco, California 94080, USA.
Thinh PhamResearch Pathology, Genentech, Inc., 1 DNA Way, South San Francisco, California 94080, USA.
Jo-Anne HongoAntibody Engineering, Genentech, Inc., 1 DNA Way, South San Francisco, California 94080, USA.
Travis BainbridgeProtein Chemistry, Genentech, Inc., 1 DNA Way, South San Francisco, California 94080, USA.
Ron FiresteinResearch Pathology, Genentech, Inc., 1 DNA Way, South San Francisco, California 94080, USA.
Elizabeth BlackwoodTranslational Oncology, Genentech, Inc., 1 DNA Way, South San Francisco, California 94080, USA.
Ciara MetcalfeTranslational Oncology, Genentech, Inc., 1 DNA Way, South San Francisco, California 94080, USA.
Eric W StawiskiMolecular Biology, Genentech, Inc., 1 DNA Way, South San Francisco, California 94080, USA.
Robert L YauchDiscovery Oncology, Genentech, Inc., 1 DNA Way, South San Francisco, California 94080, USA.
Yan WuAntibody Engineering, Genentech, Inc., 1 DNA Way, South San Francisco, California 94080, USA.
Frederic J de SauvageMolecular Oncology, Genentech, Inc., 1 DNA Way, South San Francisco, California 94080, USA.
Molecular Oncology (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Colorectal cancer remains a major unmet medical need, prompting large-scale genomics efforts in the field to identify molecular drivers for which targeted therapies might be developed. We previously reported the identification of recurrent translocations in R-spondin genes present in a subset of colorectal tumours. Here we show that targeting RSPO3 in PTPRK-RSPO3-fusion-positive human tumour xenografts inhibits tumour growth and promotes differentiation. Notably, genes expressed in the stem-cell compartment of the intestine were among those most sensitive to anti-RSPO3 treatment. This observation, combined with functional assays, suggests that a stem-cell compartment drives PTPRK-RSPO3 colorectal tumour growth and indicates that the therapeutic targeting of stem-cell properties within tumours may be a clinically relevant approach for the treatment of colorectal tumours.

Indexed as

Molecular Targeted TherapyAnimalsAntibodiesCell DifferentiationCell DivisionColorectal NeoplasmsDisease ProgressionFemaleGene Expression RegulationHumansIntestinal MucosaIntestinesMaleMiceNeoplastic Stem CellsReceptor-Like Protein Tyrosine Phosphatases, Class 2AntibodiesPTPRK protein, humanReceptor-Like Protein Tyrosine Phosphatases, Class 2RSPO3 protein, humanR-SpondinsThrombospondins

Identifiers

PMID26700806
OpenAlexW2207864075

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.