Animal studyindependent cross-checkabstract checked I-CHM-117 standard review

Tumour scar tissue can hold cancer back

Stromal elements act to restrain, rather than support, pancreatic ductal adenocarcinoma.

Overview

Rhim AD et al.. Cancer Cell 2014 · PMID 24856585 · DOI 10.1016/j.ccr.2014.04.021

In mice, removing the scar-like stroma around pancreatic tumours made them more aggressive.

Does the study support the specific claim? No · Methodological quality: moderate

Original publication

Plain-language summary

Study explained simply
What did the researchers want to find out?

Test the role of tumour stroma

How was the study done?

Mouse experiments

How many people, animals or samples were studied?

Mouse pancreatic cancer model

What was actually found?

Stroma restrains tumour growth

How large was the observed effect?

Not applicable

What do the results mean in everyday life?

Fibrosis is not simply the enemy

What are the study's limitations?

Animal model

What does it say about Elawady's specific claim?

Contradicts the simple fibrosis explanation

Do the results apply to Germany and Europe?

Low

What can explicitly not be concluded from this study?

Cannot be applied directly to patients

Scientific in-depth review

1. Full reference

Authors
Rhim AD et al.
Journal
Cancer Cell
Year
2014
Identifier
PMID 24856585 DOI 10.1016/j.ccr.2014.04.021
Verification
verified – PubMed efetch 2026-10-26 (PublicationType and CommentsCorrections checked); Crossref 2026-10-26
Retracted
no
Corrections
none
Extent checked
abstract only
Conflicts of interest and funding

NIH grants.

2. Research question

What is the role of Hedgehog-driven desmoplastic stroma in pancreatic cancer progression?

3. Study design and population

Study design
Animal study – Genetically engineered mouse model study
Population

Mouse model of pancreatic ductal adenocarcinoma

Country

USA

Period

Not stated

Sample size

Not stated in abstract

Inclusion and exclusion criteria

Mouse PDAC model

4. Methods and endpoints

Exposure / intervention

Deletion of Shh / Smoothened inhibitor (stroma depletion)

Comparator

Stroma-intact tumours

Endpoints

Tumour aggressiveness, histology, vascularity, survival

Statistical methods

Not stated in abstract

5. Actual results

Results

Shh-deficient tumours had less stroma but were more aggressive, undifferentiated, more vascular and proliferative; a Smoothened inhibitor reproduced this; VEGFR blockade improved survival of Shh-deficient tumours.

Absolute risks

not applicable (animal study)

Authors' conclusion

Some components of tumour stroma can act to restrain tumour growth.

6. Strengths

  • Genetic and pharmacological approaches agree

7. Weaknesses

  • Mouse model; one tumour type

8. Risk of bias

Orienting tool
none applicable
Type of assessment
simplified assessment (abstract only)
Full formal assessment
no
Overall risk of bias
not assessable
Rationale

Animal study.

9. Assessment of the statistical interpretation

Not applicable.

10. Relevance to the specific claim

Contradicts the claim that fibrotic stroma simply drives cancer: removing stroma made tumours more aggressive.

11. Independent contrary findings

Olive 2009 (I-CHM-11) and Meads 2009 (I-CHM-119): stroma can impede drug delivery or protect cells.

12. Transferability to Germany and Europe

Basic biology.

13. Overall methodological judgement

Shows stroma has dual roles.

Multidimensional assessment
Multidimensional assessment
Authenticity of the sourceverified
Methodological qualitymoderate
Risk of biasnot assessable
Precision of resultsnot applicable
Directnessvery indirect
Reproducibilityreplicated
Consistency with the overall evidenceconsistent
Regional transferabilitylow
Adequacy of the interpretation (by the archive)not applicable

14. Open questions

Human relevance.

15. Linked fact checks