Evidence map›Paper›PMID 30469497›Full record

ArticleCancers2018

ISG15 Promotes ERK1 ISGylation, CD8+ T Cell Activation and Suppresses Ovarian Cancer Progression.

Tsz-Lun Yeung, Ching Chou Tsai, Cecilia S Leung, Chi-Lam Au Yeung, Melissa S Thompson, Karen H Lu, Ralph S Freedman, Michael J Birrer, Kwong-Kwok Wong, Samuel C Mok

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
3.2field-weighted citation impact, top 8% 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

30 citing papers in PubMed, 47 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
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  8. Article
  9. Molecular Interplay of ISG15/ISGylation in Neuropathologies.CNS & neurological disorders drug targets · 2025
    Review
  10. Article
  11. Article
  12. Article
  13. Review
  14. ISG15: A link between innate immune signaling, DNA replication, and genome stability.BioEssays : news and reviews in molecular, cellular and developmental biology · 2023
    Review
  15. Review
  16. Review
  17. Review
  18. Article
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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

10 authors at 2 institutions in 2 countries.

Tsz-Lun YeungDepartment of Gynecologic Oncology and Reproductive Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA. tyeung@mdanderson.org.
Ching Chou TsaiDepartment of Gynecologic Oncology and Reproductive Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA. nick58tsai@gmail.com.
Cecilia S LeungDepartment of Gynecologic Oncology and Reproductive Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA. slleung@mdanderson.org.
Chi-Lam Au YeungDepartment of Gynecologic Oncology and Reproductive Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA. CAu@mdanderson.org.
Melissa S ThompsonDepartment of Gynecologic Oncology and Reproductive Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA. Melissa.Thompson@uth.tmc.edu.
Karen H LuDepartment of Gynecologic Oncology and Reproductive Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA. khlu@mdanderson.org.
Ralph S FreedmanDepartment of Gynecologic Oncology and Reproductive Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA. freedmanralphs@gmail.com.
Michael J BirrerComprehensive Cancer Center, Division of Hematology-Oncology, University of Alabama at Birmingham, Birmingham, AL 35294, USA. mbirrer@uab.edu.
Kwong-Kwok WongDepartment of Gynecologic Oncology and Reproductive Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA. kkwong@mdanderson.org.ORCID 0000-0002-0375-6669
Samuel C MokDepartment of Gynecologic Oncology and Reproductive Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA. scmok@mdanderson.org.
The University of Texas MD Anderson Cancer Center · USUniversity of Alabama at Birmingham · US

Funding

UNIVERSITY OF TEXAS MD ANDERSON SPORE IN OVARIAN CANCERP50CA083639 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI BAST, ROBERT C · 1999 to 2015
$33.0M
Training in Oncology Population Sciences (TOPS)T32CA092203 · NCI · DANA-FARBER CANCER INST · PI Nancy L Keating, JENNIFER W MACK · 2018 to 2026
$3.7M
The FGF18/FGFR4 amplicon: Novel therapeutic biomarkers for ovarian cancerR01CA169200 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI BIRRER, MICHAEL, MOK, SAMUEL C · 2013 to 2017
$1.9M
Novel Biomarkers in Ovarian CancerR01CA142832 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI BIRRER, MICHAEL · 2010 to 2014
$1.7M
NCI NIH HHS R01 CA142832NCI NIH HHS R01 CA169200NIH HHS P50CA083639NIH HHS R01CA142832NIH HHS R01CA169200U.S. Department of Defense W81XWH-17-1-0126
6 · The paper itself

Abstract

Increased number of tumor-infiltrating CD8+ lymphocytes is associated with improved survival in patients with advanced stage high grade serous ovarian cancer (HGSOC) but the underlying molecular mechanism has not been thoroughly explored. Using transcriptome profiling of microdissected HGSOC tissue with high and low CD8+ lymphocyte count and subsequent validation studies, we demonstrated that significantly increased ISG15 (Interferon-stimulated gene 15) expression in HGSOC was associated with high CD8+ lymphocyte count and with the improvement in median overall survival in both univariate and multivariate analyses. Further functional studies showed that endogenous and exogenous ISG15 suppressed ovarian cancer progression through ISGylation of ERK in HGSOC, and activation of NK cells and CD8+ T lymphocytes. These data suggest that the development of treatment strategies based on up-regulating ISG15 in ovarian cancer cells or increased circulating ISG15 in ovarian cancer patients is warranted.

Indexed as

CD8+ lymphocyteinterferonISG15ISGylationovarian cancer

Identifiers

PMID30469497
PMCPMC6316352
OpenAlexW2900532815

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.