Evidence map›Paper›PMID 38979935›Full record

ArticleCytoskeleton (Hoboken, N.J.)2024

Enhanced RHO-ROCK signaling is associated with CRELD2 production and fibroblast recruitment in cutaneous squamous cell carcinoma.

Alexandra Pittar, Edward J Buckley, Sarah T Boyle, S Jan Ibbetson, Michael S Samuel

Abstract read
In one paragraph

Article in Cytoskeleton (Hoboken, N.J.), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Integrative omics profiling of CRELD2 in ccRCC: a nexus of genetics, prognosis, and tumor microenvironment.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2026
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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.

Alexandra PittarCentre for Cancer Biology, an Alliance between SA Pathology and the University of South Australia, Adelaide, Australia.ORCID https://orcid.org/0009-0008-8228-8293
Edward J BuckleyCentre for Cancer Biology, an Alliance between SA Pathology and the University of South Australia, Adelaide, Australia.ORCID https://orcid.org/0000-0002-4736-4608
Sarah T BoyleCentre for Cancer Biology, an Alliance between SA Pathology and the University of South Australia, Adelaide, Australia.ORCID https://orcid.org/0000-0001-6143-9285
S Jan IbbetsonDivision of Surgical Pathology, SA Pathology, Adelaide, Australia.
Michael S SamuelCentre for Cancer Biology, an Alliance between SA Pathology and the University of South Australia, Adelaide, Australia.ORCID https://orcid.org/0000-0001-7880-6379

Funding

Australian Research CouncilCancer Council SA's Beat Cancer ProjectHospital Research FoundationNational Health and Medical Research CouncilRoyal Adelaide Hospital Research Fund
6 · The paper itself

Abstract

A key characteristic of cancer cells is their ability to induce changes in their microenvironment that render it permissive to tumor growth, invasion and metastasis. Indeed, these changes are required for tumor progression. Consequently, the tumor microenvironment is emerging as a key source of new targets against cancer, with novel therapies aimed at reversing tumor-promoting changes, reinstating a tumor-hostile microenvironment and suppressing disease progression. RHO-ROCK signaling, and consequent tension within the cellular actomyosin cytoskeleton, regulates a paracrine signaling cascade that establishes a tumor-promoting microenvironment. Here, we show that consistent with our observations in breast cancer, enhanced ROCK activity and consequent production of CRELD2 is associated with the recruitment and tumor-promoting polarization of cancer-associated fibroblasts in cutaneous squamous cell carcinoma. Our observations provide support for the notion that the role of RHO-ROCK signaling in establishing a tumor-promoting microenvironment may be conserved across patients and potentially also different cancer types.

Indexed as

Carcinoma, Squamous CellFibroblastsrho-Associated KinasesSignal TransductionSkin NeoplasmsCancer-Associated FibroblastsCell Line, TumorHumansrho GTP-Binding ProteinsTumor Microenvironmentrho-Associated Kinasesrho GTP-Binding Proteinscancer‐associated fibroblastsCRELD2cutaneous squamous cell carcinomaextracellular matrixRHO‐ROCK signaling

Identifiers

PMID38979935
PMCPMC11615837

What OpenQuestion holds

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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.