Evidence map›Paper›PMID 38140561›Full record

ArticleViruses2023

Emerging Prognostic and Predictive Significance of Stress Keratin 17 in HPV-Associated and Non HPV-Associated Human Cancers: A Scoping Review.

Taja Lozar, Wei Wang, Niki Gavrielatou, Leslie Christensen, Paul F Lambert, Paul M Harari, David L Rimm, Barbara Burtness, Cvetka Grasic Kuhar, Evie H Carchman

Open access · goldAbstract readScoping Review
In one paragraph

Article in Viruses, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.8field-weighted citation impact, top 27% 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

4 citing papers in PubMed, 4 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. 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.

Taja LozarMcArdle Laboratory for Cancer Research, University of Wisconsin School of Medicine and Public Health, Madison, WI 53705, USA.ORCID 0000-0003-2893-5580
Wei WangMcArdle Laboratory for Cancer Research, University of Wisconsin School of Medicine and Public Health, Madison, WI 53705, USA.
Niki GavrielatouDepartment of Pathology, Yale University, New Haven, CT 06510, USA.ORCID 0000-0003-1380-6831
Leslie ChristensenEbling Library, University of Wisconsin School of Medicine and Public Health, Madison, WI 53705, USA.ORCID 0000-0002-4040-5593
Paul F LambertMcArdle Laboratory for Cancer Research, University of Wisconsin School of Medicine and Public Health, Madison, WI 53705, USA.ORCID 0000-0001-7983-2755
Paul M HarariUniversity of Wisconsin Carbone Cancer Center, Madison, WI 53705, USA.
David L RimmDepartment of Pathology, Yale University, New Haven, CT 06510, USA.ORCID 0000-0001-5820-4397
Barbara BurtnessDepartment of Medicine and Yale Cancer Center, Yale School of Medicine, New Haven, CT 06510, USA.
Cvetka Grasic KuharUniversity of Ljubljana, 1000 Ljubljana, Slovenia.ORCID 0000-0001-5047-4034
Evie H CarchmanUniversity of Wisconsin Carbone Cancer Center, Madison, WI 53705, USA.ORCID 0000-0002-5536-7761
University of Wisconsin–Madison · USYale University · USUniversity of Ljubljana · SIYale Cancer Center · US

Funding

UW COMPREHENSIVE CANCER CENTER SUPPORTP30CA014520 · NCI · UNIVERSITY OF WISCONSIN-MADISON · PI AMY TRENTHAM-DIETZ · 1985 to 2026
$142.6M
Yale Clinical and Translational Science Award (U Component)UL1TR001863 · NCATS · YALE UNIVERSITY · PI John H. Krystal, LUCILA OHNO-MACHADO · 2016 to 2026
$102.9M
Visualizing EBV and HCMV DNA Dynamics During InfectionP01CA022443 · NCI · UNIVERSITY OF WISCONSIN-MADISON · PI WILLIAM M. SUGDEN · 1985 to 2026
$53.1M
Project 3: Modulation of the head and neck tumor immune microenvironment by targeting the TAM family of receptorsP50CA278595 · NCI · UNIVERSITY OF WISCONSIN-MADISON · PI PAUL M HARARI · 2022 to 2026
$12.5M
Yale Head and Neck Cancer SPORE: Overcoming Treatment Resistance in Head and Neck CancerP50DE030707 · NIDCR · YALE UNIVERSITY · PI TOWNSEND, JEFFREY PETER · 2020 to 2024
$11.8M
Defining Drivers of HPV-associated CarcinogenesisR35CA210807 · NCI · UNIVERSITY OF WISCONSIN-MADISON · PI Paul F. Lambert · 2017 to 2026
$9.2M
Mouse Model of Human Papillomavirus PathogenesisR01CA228543 · NCI · TUFTS UNIVERSITY BOSTON · PI LAMBERT, PAUL F., MUNGER, KARL · 2019 to 2023
$2.3M
NCATS NIH HHS UL1 TR001863NCI NIH HHS P01 CA022443NCI NIH HHS P30 CA014520NCI NIH HHS P50 CA278595NCI NIH HHS R01 CA228543NCI NIH HHS R35 CA210807NIDCR NIH HHS P50 DE030707NIH HHS CA022443NIH HHS P01 CA022443NIH HHS P30CA014520-49NIH HHS P50 CA278595NIH HHS R01 CA228543NIH HHS R35 CA210807
6 · The paper itself

Abstract

A growing body of literature suggests that the expression of cytokeratin 17 (K17) correlates with inferior clinical outcomes across various cancer types. In this scoping review, we aimed to review and map the available clinical evidence of the prognostic and predictive value of K17 in human cancers. PubMed, Web of Science, Embase (via Scopus), Cochrane Central Register of Controlled Trials, and Google Scholar were searched for studies of K17 expression in human cancers. Eligible studies were peer-reviewed, published in English, presented original data, and directly evaluated the association between K17 and clinical outcomes in human cancers. Of the 1705 studies identified in our search, 58 studies met criteria for inclusion. Studies assessed the prognostic significance (n = 54), predictive significance (n = 2), or both the prognostic and predictive significance (n = 2). Altogether, 11 studies (19.0%) investigated the clinical relevance of K17 in cancers with a known etiologic association to HPV; of those, 8 (13.8%) were focused on head and neck squamous cell carcinoma (HNSCC), and 3 (5.1%) were focused on cervical squamous cell carcinoma (SCC). To date, HNSCC, as well as triple-negative breast cancer (TNBC) and pancreatic cancer, were the most frequently studied cancer types. K17 had prognostic significance in 16/17 investigated cancer types and 43/56 studies. Our analysis suggests that K17 is a negative prognostic factor in the majority of studied cancer types, including HPV-associated types such as HNSCC and cervical cancer (13/17), and a positive prognostic factor in 2/17 studied cancer types (urothelial carcinoma of the upper urinary tract and breast cancer). In three out of four predictive studies, K17 was a negative predictive factor for chemotherapy and immune checkpoint blockade therapy response.

Indexed as

Carcinoma, Squamous CellCarcinoma, Transitional CellHead and Neck NeoplasmsKeratin-17Papillomavirus InfectionsUrinary Bladder NeoplasmsUterine Cervical NeoplasmsBiomarkers, TumorFemaleHumansPrognosisSquamous Cell Carcinoma of Head and NeckBiomarkers, TumorKeratin-17cytokeratin 17predictive biomarkerprognostic biomarkerstress keratin 17

Identifiers

PMID38140561
PMCPMC10748233
OpenAlexW4389051508

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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.