Evidence map›Paper›PMID 25695953›Full record

ArticleMolecular cancer therapeutics2015

A novel neutralizing antibody targeting pregnancy-associated plasma protein-a inhibits ovarian cancer growth and ascites accumulation in patient mouse tumorgrafts.

Marc A Becker, Paul Haluska, Laurie K Bale, Claus Oxvig, Cheryl A Conover

Open access · greenAbstract read
In one paragraph

Article in Molecular cancer therapeutics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
5.4field-weighted citation impact, top 4% 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

40 citing papers in PubMed, 59 citations in OpenAlex.

  1. Article
  2. Pan-Cancer Analysis ofBiology · 2026
    Article
  3. Article
  4. IGF Pathway Components as Potential Biomarkers in Gastric Cancer.International journal of molecular sciences · 2025
    Article
  5. Article
  6. Article
  7. PAPP-A as a Potential Target in Thyroid Eye Disease.The Journal of clinical endocrinology and metabolism · 2024
    Article
  8. Review
  9. Review
  10. Article
  11. Article
  12. Article
  13. The Proteolytic Landscape of Ovarian Cancer: Applications in Nanomedicine.International journal of molecular sciences · 2022
    Review
  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. Review
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 at 2 institutions in 2 countries.

Marc A BeckerDivision of Medical Oncology, Mayo Clinic, Rochester, Minnesota.
Paul HaluskaDivision of Medical Oncology, Mayo Clinic, Rochester, Minnesota.
Laurie K BaleDivision of Endocrinology, Mayo Clinic, Rochester, Minnesota.
Claus OxvigDepartment of Molecular Biology and Genetics, Aarhus University, Aarhus, Denmark.
Cheryl A ConoverDivision of Endocrinology, Mayo Clinic, Rochester, Minnesota. conover.cheryl@mayo.edu.
Mayo Clinic · USAarhus University · DK

Funding

Use of microfluidic tumor cultures to enable clinical trials of therapies for ovarian cancerP50CA136393 · NCI · MAYO CLINIC ROCHESTER · PI Zhenkun Lou · 2009 to 2026
$37.0M
DIABETES AND METABOLISMT32DK007352 · NIDDK · MAYO CLINIC ROCHESTER · PI MICHAEL D. JENSEN · 1986 to 2026
$9.4M
NCI NIH HHS CA136393NCI NIH HHS P50 CA136393NIDDK NIH HHS T32 DK007352NIDDK NIH HHS T32 DK07352
6 · The paper itself

Abstract

The majority of ovarian cancer patients acquire resistance to standard platinum chemotherapy and novel therapies to reduce tumor burden and ascites accumulation are needed. Pregnancy-associated plasma protein-A (PAPP-A) plays a key role in promoting insulin-like growth factor (IGF) pathway activity, which directly correlates to ovarian cancer cell transformation, growth, and invasiveness. Herein, we evaluate PAPP-A expression in tumors and ascites of women with ovarian cancer, and determine the antitumor efficacy of a neutralizing monoclonal PAPP-A antibody (mAb-PA) in ovarian cancer using primary patient ovarian tumorgrafts ("Ovatars"). PAPP-A mRNA expression in patient ovarian tumors correlated with poor outcome and was validated as a prognostic surrogate in Ovatar tumors. Following confirmation of mAb-PA bioavailability and target efficacy in vivo, the antitumor efficacy of mAb-PA in multiple Ovatar tumor models was examined and the response was found to depend on PAPP-A expression. Strikingly, the addition of mAb-PA to standard platinum chemotherapy effectively sensitized platinum-resistant Ovatar tumors. PAPP-A protein in ascites was also assessed in a large cohort of patients and very high levels were evident across the entire sample set. Therefore, we evaluated targeted PAPP-A inhibition as a novel approach to managing ovarian ascites, and found that mAb-PA inhibited the development, attenuated the progression, and induced the regression of Ovatar ascites. Together, these data indicate PAPP-A as a potential palliative and adjunct therapeutic target for women with ovarian cancer.

Indexed as

AnimalsAntibodies, MonoclonalAntibodies, NeutralizingAntineoplastic AgentsAscitesCarboplatinCell Line, TumorDisease Models, AnimalFemaleGene ExpressionHumansImmunohistochemistryMiceOvarian NeoplasmsPaclitaxelPregnancy-Associated Plasma Protein-AAntibodies, MonoclonalAntibodies, NeutralizingAntineoplastic AgentsCarboplatinPaclitaxelPregnancy-Associated Plasma Protein-A

Identifiers

PMID25695953
PMCPMC4394033
OpenAlexW2120623956

What OpenQuestion holds

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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.