Evidence map›Paper›PMID 31332047›Full record

ArticleClinical cancer research : an official journal of the American Association for Cancer Research2019

Anticancer Immunotherapy by MFAP5 Blockade Inhibits Fibrosis and Enhances Chemosensitivity in Ovarian and Pancreatic Cancer.

Tsz-Lun Yeung, Cecilia S Leung, Kay-Pong Yip, Jianting Sheng, Long Vien, Laura C Bover, Michael J Birrer, Stephen T C Wong, Samuel C Mok

Open access · bronzeAbstract read
In one paragraph

Article in Clinical cancer research : an official journal of the American Association for Cancer Research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed
2.5field-weighted citation impact, top 10% 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

54 citing papers in PubMed, 73 citations in OpenAlex.

  1. Understanding and targeting the tumour matrisome.Nature reviews. Clinical oncology · 2026
    Review
  2. Article
  3. MFAP5iScience · 2026
    Article
  4. Identification ofTranslational cancer research · 2026
    Article
  5. Article
  6. Article
  7. Molecular mechanisms of ovarian fibrosis.Molecular human reproduction · 2026
    Review
  8. Loss of MFAP5 and Its Effect on Skin Homeostasis and Wound Healing.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2025
    Article
  9. Review
  10. Article
  11. Article
  12. ZP4: A novel target for CAR-T cell therapy in triple negative breast cancer.Molecular therapy : the journal of the American Society of Gene Therapy · 2025
    Article
  13. Pancreatic cancer-derived extracellular vesicles enhance chemoresistance by delivering KRASMolecular therapy : the journal of the American Society of Gene Therapy · 2025
    Article
  14. Article
  15. Article
  16. Loss of phosphatase and tensin homolog (Cancer pathogenesis and therapy · 2025
    Article
  17. Review
  18. Article
  19. Review
  20. 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

9 authors at 5 institutions in 1 country.

Tsz-Lun Yeung *Department of Gynecologic Oncology and Reproductive Medicine, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Cecilia S Leung *Department of Gynecologic Oncology and Reproductive Medicine, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Kay-Pong YipDepartment of Molecular Pharmacology and Physiology, University of South Florida, Tampa, Florida.ORCID 0000-0003-4364-6701
Jianting ShengDepartment of Systems Medicine and Bioengineering, Houston Methodist Cancer Center, Weill Cornell Medical College, Houston, Texas.
Long VienDepartment of Immunology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Laura C BoverDepartment of Genomic Medicine, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Michael J BirrerDepartment of Medicine, University of Alabama at Birmingham, Birmingham, Alabama. scmok@mdanderson.org mbirrer@uab.edu stwong@houstonmethodist.org.
Stephen T C WongDepartment of Systems Medicine and Bioengineering, Houston Methodist Cancer Center, Weill Cornell Medical College, Houston, Texas. scmok@mdanderson.org mbirrer@uab.edu stwong@houstonmethodist.org.
Samuel C MokDepartment of Gynecologic Oncology and Reproductive Medicine, The University of Texas MD Anderson Cancer Center, Houston, Texas. scmok@mdanderson.org mbirrer@uab.edu stwong@houstonmethodist.org.
The University of Texas MD Anderson Cancer Center · USCornell University · USHouston Methodist · USUniversity of Alabama at Birmingham · USUniversity of South Florida · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Fabien Delerue · 1985 to 2026
$290.8M
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
Genomic Stratification of Ovarian Cancer PatientsRC4CA156551 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI BIRRER, MICHAEL · 2010 to 2010
$3.7M
Targeting Stromal Influences on Glutamine Addiction in Ovarian CancerR01CA227622 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI MOK, SAMUEL C, NAGRATH, DEEPAK · 2018 to 2022
$2.3M
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
Prognostic markers for ovarian cancerR01CA133057 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI MOK, SAMUEL C · 2009 to 2013
$1.5M
NCI NIH HHS P30 CA016672NCI NIH HHS P50 CA083639NCI NIH HHS R01 CA133057NCI NIH HHS R01 CA142832NCI NIH HHS R01 CA169200NCI NIH HHS R01 CA227622NCI NIH HHS RC4 CA156551
6 · The paper itself

Abstract

purposeRecent studies demonstrate the role of the tumor microenvironment in tumor progression. However, strategies used to overcome the malignant phenotypes of cancer cells modulated by the microenvironment have not been thoroughly explored. In this study, we evaluated the therapeutic efficacy of a newly developed mAb targeting microfibril-associated protein 5 (MFAP5), which is secreted predominately by cancer-associated fibroblast (CAF), in ovarian and pancreatic cancer models.

resultsThree hybridoma clones, which produced antibodies with high affinity and specificity to MFAP5, were selected for functional studies. Antibody clone 130A, which recognizes a common epitope shared between human and murine MFAP5 protein, was further selected for

conclusionsThese data suggest that MFAP5 blockade using an immunologic approach inhibits fibrosis, induces tumor vessel normalization, and enhances chemosensitivity in ovarian and pancreatic cancer, and can be used as a novel therapeutic agent.

Indexed as

AnimalsCancer-Associated FibroblastsCell Line, TumorCell MovementContractile ProteinsDisease ProgressionFemaleFibrosisGene Expression Regulation, NeoplasticHumansImmunotherapyIntercellular Signaling Peptides and ProteinsMiceOvarian NeoplasmsPancreatic NeoplasmsSignal TransductionContractile ProteinsIntercellular Signaling Peptides and ProteinsMFAP5 protein, human

Identifiers

PMID31332047
PMCPMC6825539
OpenAlexW2963503733

What OpenQuestion holds

Textmetadata
LicenceTDM
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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.