Evidence map›Paper›PMID 34584216›Full record

ArticleOncogene2021

Mutant collagen COL11A1 enhances cancerous invasion.

Carolyn S Lee, Zurab Siprashvili, Angela Mah, Tomas Bencomo, Lara E Elcavage, Yonglu Che, Rajani M Shenoy, Sumaira Z Aasi, Paul A Khavari

Abstract read
In one paragraph

Article in Oncogene, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
–field-weighted citation impact
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

22 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. The Multifaced Role of Collagen in Cancer Development and Progression.International journal of molecular sciences · 2024
    Review
  7. Review
  8. Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Review
  19. Article
  20. 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

9 authors.

Carolyn S LeeStanford Program in Epithelial Biology, Stanford University, Stanford, CA, 94305, USA. carilee@stanford.edu.ORCID http://orcid.org/0000-0002-6511-3757
Zurab SiprashviliStanford Program in Epithelial Biology, Stanford University, Stanford, CA, 94305, USA.
Angela MahStanford Program in Epithelial Biology, Stanford University, Stanford, CA, 94305, USA.
Tomas BencomoStanford Program in Epithelial Biology, Stanford University, Stanford, CA, 94305, USA.
Lara E ElcavageStanford Program in Epithelial Biology, Stanford University, Stanford, CA, 94305, USA.
Yonglu CheStanford Program in Epithelial Biology, Stanford University, Stanford, CA, 94305, USA.
Rajani M ShenoyStanford Program in Epithelial Biology, Stanford University, Stanford, CA, 94305, USA.
Sumaira Z AasiStanford Program in Epithelial Biology, Stanford University, Stanford, CA, 94305, USA.
Paul A KhavariStanford Program in Epithelial Biology, Stanford University, Stanford, CA, 94305, USA. khavari@stanford.edu.ORCID http://orcid.org/0000-0003-0098-4989

Funding

Mechanisms of Epidermal Homeostasis and Early NeoplasiaR01AR043799 · NIAMS · STANFORD UNIVERSITY · PI PAUL KHAVARI · 1998 to 2026
$9.1M
Regulators of TumorigenesisR01CA142635 · NCI · STANFORD UNIVERSITY · PI KHAVARI, PAUL · 2011 to 2020
$3.5M
REGULATORS OF EPITHELIAL TUMOR PROGRESSIONI01BX001409 · VA · VETERANS ADMIN PALO ALTO HEALTH CARE SYS · PI KHAVARI, PAUL · 2012 to 2025
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BLRD VA I01 BX001409NCI NIH HHS R01 CA142635NIAMS NIH HHS R01 AR043799
6 · The paper itself

Abstract

Collagens are the most abundant proteins in the body and comprise the basement membranes and stroma through which cancerous invasion occurs; however, a pro-neoplastic function for mutant collagens is undefined. Here we identify COL11A1 mutations in 66 of 100 cutaneous squamous cell carcinomas (cSCCs), the second most common U.S. cancer, concentrated in a triple helical region known to produce trans-dominant collagens. Analysis of COL11A1 and other collagen genes found that they are mutated across common epithelial malignancies. Knockout of mutant COL11A1 impairs cSCC tumorigenesis in vivo. Compared to otherwise genetically identical COL11A1 wild-type tissue, gene-edited mutant COL11A1 skin is characterized by induction of β1 integrin targets and accelerated neoplastic invasion. In mosaic tissue, mutant COL11A1 cells enhanced invasion by neighboring wild-type cells. These results suggest that specific collagens are commonly mutated in cancer and that mutant collagens may accelerate this process.

Indexed as

MutationAnimalsCarcinoma, Squamous CellCase-Control StudiesCollagen Type XIExome SequencingFemaleHumansIntegrin beta1MiceNeoplasm InvasivenessNeoplasm TransplantationProtein Structure, SecondarySkin NeoplasmsCOL11A1 protein, humanCollagen Type XIIntegrin beta1Itgb1 protein, human

Identifiers

PMID34584216
PMCPMC8566234

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Registered trials

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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.