Evidence map›Paper›PMID 36428658›Full record

ReviewCancers2022

Chondroitin Sulfate Proteoglycan 4 as a Marker for Aggressive Squamous Cell Carcinoma.

Kathryn Chen, Joel Yong, Roland Zauner, Verena Wally, John Whitelock, Mila Sajinovic, Zlatko Kopecki, Kang Liang, Kieran Francis Scott, Albert Sleiman Mellick

Open access · goldAbstract readReview
In one paragraph

Review in Cancers, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.4field-weighted citation impact, top 21% 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

14 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Review
  11. Article
  12. Article
  13. Role of autophagy in angiogenic potential of vascular pericytes.Frontiers in cell and developmental biology · 2024
    Review
  14. 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

10 authors at 4 institutions in 2 countries.

Kathryn ChenIngham Institute for Applied Medical Research, Medicine, University of New South Wales, Liverpool, NSW 2170, Australia.
Joel YongIngham Institute for Applied Medical Research, Medicine, University of New South Wales, Liverpool, NSW 2170, Australia.
Roland ZaunerEB House Austria, Research Program for Molecular Therapy of Genodermatoses, Department of Dermatology & Allergology, University Hospital of the Paracelsus Medical University, 5020 Salzburg, Austria.
Verena WallyEB House Austria, Research Program for Molecular Therapy of Genodermatoses, Department of Dermatology & Allergology, University Hospital of the Paracelsus Medical University, 5020 Salzburg, Austria.ORCID 0000-0001-8705-3890
John WhitelockIngham Institute for Applied Medical Research, Medicine, University of New South Wales, Liverpool, NSW 2170, Australia.
Mila SajinovicIngham Institute for Applied Medical Research, Medicine, University of New South Wales, Liverpool, NSW 2170, Australia.
Zlatko KopeckiFuture Industries Institute, University of South Australia, Mawson Lakes, SA 5095, Australia.ORCID 0000-0002-8072-4222
Kang LiangIngham Institute for Applied Medical Research, Medicine, University of New South Wales, Liverpool, NSW 2170, Australia.ORCID 0000-0003-3985-7688
Kieran Francis ScottIngham Institute for Applied Medical Research, Medicine, University of New South Wales, Liverpool, NSW 2170, Australia.ORCID 0000-0002-6012-4107
Albert Sleiman MellickIngham Institute for Applied Medical Research, Medicine, University of New South Wales, Liverpool, NSW 2170, Australia.
UNSW Sydney · AUCamden and Campbelltown Hospitals · AUParacelsus Medical University · ATUniversity of South Australia · AU

Funding

DEBRA Australia NA
6 · The paper itself

Abstract

Chondroitin sulfate (CS) proteoglycan 4 (CSPG4) is a cell surface proteoglycan that is currently under investigation as a marker of cancer malignancy, and as a potential target of anticancer drug treatment. CSPG4 acts as a driver of tumourigenesis by regulating turnover of the extracellular matrix (ECM) to promote tumour cell invasion, migration as well as inflammation and angiogenesis. While CSPG4 has been widely studied in certain malignancies, such as melanoma, evidence is emerging from global gene expression studies, which suggests a role for CSPG4 in squamous cell carcinoma (SCC). While relatively treatable, lack of widely agreed upon diagnostic markers for SCCs is problematic, especially for clinicians managing certain patients, including those who are aged or infirm, as well as those with underlying conditions such as epidermolysis bullosa (EB), for which a delayed diagnosis is likely lethal. In this review, we have discussed the structure of CSPG4, and quantitatively analysed CSPG4 expression in the tissues and pathologies where it has been identified to determine the usefulness of CSPG4 expression as a diagnostic marker and therapeutic target in management of malignant SCC.

Indexed as

cancer biomarkerchondroitin sulfate proteoglycancutaneous squamous cell carcinomagene expressionhead and neck squamous cell carcinoma

Identifiers

PMID36428658
PMCPMC9688099
OpenAlexW4308970195

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.