Evidence map›Paper›PMID 38067116›Full record

ArticleCells2023

Dynamics of Fibril Collagen Remodeling by Tumor Cells: A Model of Tumor-Associated Collagen Signatures.

Sharan Poonja, Ana Forero Pinto, Mark C Lloyd, Mehdi Damaghi, Katarzyna A Rejniak

Abstract read
In one paragraph

Article in Cells, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Collagen remodeling in breast cancer progression: from molecular mechanisms to diagnostic and therapeutic opportunities.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. The Multifaced Role of Collagen in Cancer Development and Progression.International journal of molecular sciences · 2024
    Review
  9. Review
  10. Article
  11. Article
  12. Spatial interactions modulate tumor growth and immune infiltration.bioRxiv : the preprint server for biology · 2024
    Article
  13. 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

5 authors.

Sharan PoonjaIntegrated Mathematical Oncology Department, H. Lee Moffitt Cancer Center, Research Institute, Tampa, FL 33612, USA.ORCID 0000-0002-1682-7980
Ana Forero PintoIntegrated Mathematical Oncology Department, H. Lee Moffitt Cancer Center, Research Institute, Tampa, FL 33612, USA.
Mark C LloydFujifilm Healthcare US, Inc., Lexington, MA 02421, USA.
Mehdi DamaghiDepartment of Pathology, Renaissance School of Medicine, Stony Brook University, Stony Brook, NY 11794, USA.
Katarzyna A RejniakIntegrated Mathematical Oncology Department, H. Lee Moffitt Cancer Center, Research Institute, Tampa, FL 33612, USA.ORCID 0000-0003-2093-2422

Funding

TRANSLATIONAL RESEARCHP30CA076292 · NCI · UNIVERSITY OF SOUTH FLORIDA · PI John L. Cleveland · 1998 to 2026
$93.5M
Prevention of MGUS Progression to MM by Modulating the Bone Marrow MicroenvironmentU54CA272691 · NCI · CHILDREN'S MERCY HOSP (KANSAS CITY, MO) · PI John Damian Shaughnessy · 2023 to 2026
$6.1M
Ecology and Evolution of Breast CarcinogenesisU01CA261841 · NCI · STATE UNIVERSITY NEW YORK STONY BROOK · PI DAMAGHI, MEHDI, SIQUEIRA SILVA, ARIOSTO S · 2021 to 2025
$3.0M
Physical Dynamics of Cancer Response to Chemotherapy in 3D MicroenvironmentsU01CA202229 · NCI · VANDERBILT UNIVERSITY · PI MARKOV, DMITRY, MCCAWLEY, LISA JOY · 2015 to 2019
$3.0M
Modeling the role and regulation of reactive stroma in breast ductal carcinoma microinvasionsR01CA272601 · NCI · H. LEE MOFFITT CANCER CTR & RES INST · PI DAMAGHI, MEHDI, REJNIAK, KATARZYNA ANNA · 2022 to 2025
$2.9M
NCI NIH HHS P30 CA076292NCI NIH HHS R01 CA272601NCI NIH HHS U01 CA202229NCI NIH HHS U01 CA261841NCI NIH HHS U54 CA272691
6 · The paper itself

Abstract

Many solid tumors are characterized by a dense extracellular matrix (ECM) composed of various ECM fibril proteins. These proteins provide structural support and a biological context for the residing cells. The reciprocal interactions between growing and migrating tumor cells and the surrounding stroma result in dynamic changes in the ECM architecture and its properties. With the use of advanced imaging techniques, several specific patterns in the collagen surrounding the breast tumor have been identified in both tumor murine models and clinical histology images. These tumor-associated collagen signatures (TACS) include loosely organized fibrils far from the tumor and fibrils aligned either parallel or perpendicular to tumor colonies. They are correlated with tumor behavior, such as benign growth or invasive migration. However, it is not fully understood how one specific fibril pattern can be dynamically remodeled to form another alignment. Here, we present a novel multi-cellular lattice-free (

Indexed as

CollagenNeoplasmsAnimalsExtracellular MatrixExtracellular Matrix ProteinsFibrillar CollagensMiceCollagenExtracellular Matrix ProteinsFibrillar Collagensagent-based modelsECM fibril patternsextracellular matrix (ECM)in silico modelingMultiCell-LF modelTumor-Associated Collagen Signature (TACS)tumor-ECM interactionstumor microenvironment

Identifiers

PMID38067116
PMCPMC10705683

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.