Evidence map›Paper›PMID 32409304›Full record

ArticleClinical cancer research : an official journal of the American Association for Cancer Research2020

Arginine Depletion Therapy with ADI-PEG20 Limits Tumor Growth in Argininosuccinate Synthase-Deficient Ovarian Cancer, Including Small-Cell Carcinoma of the Ovary, Hypercalcemic Type.

Jennifer X Ji, Dawn R Cochrane, Basile Tessier-Cloutier, Shary Yutin Chen, Germain Ho, Khyatiben V Pathak, Isabel N Alcazar, David Farnell, Samuel Leung, Angela Cheng and 14 more

Open access · greenAbstract read
In one paragraph

Article in Clinical cancer research : an official journal of the American Association for Cancer Research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
3.0field-weighted citation impact, top 9% 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

25 citing papers in PubMed, 35 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. Review
  7. Review
  8. Article
  9. Article
  10. Review
  11. Article
  12. Review
  13. Review
  14. Review
  15. Article
  16. Review
  17. Article
  18. Article
  19. Article
  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

24 authors at 8 institutions in 3 countries.

Jennifer X JiDepartment of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, Canada.
Dawn R CochraneDepartment of Molecular Oncology, BC Cancer Agency, Vancouver, Canada.
Basile Tessier-CloutierDepartment of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, Canada.ORCID 0000-0001-8739-3879
Shary Yutin ChenDepartment of Molecular Oncology, BC Cancer Agency, Vancouver, Canada.
Germain HoDepartment of Molecular Oncology, BC Cancer Agency, Vancouver, Canada.
Khyatiben V PathakCollaborative Center for Translational Mass Spectrometry, The Translational Genomics Research Institute, Phoenix, Arizona.
Isabel N AlcazarCollaborative Center for Translational Mass Spectrometry, The Translational Genomics Research Institute, Phoenix, Arizona.
David FarnellDepartment of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, Canada.ORCID 0000-0001-8589-4354
Samuel LeungGenetic Pathology Evaluation Center, Vancouver, Canada.
Angela ChengGenetic Pathology Evaluation Center, Vancouver, Canada.
Christine ChowGenetic Pathology Evaluation Center, Vancouver, Canada.ORCID 0000-0001-5098-5731
Shane ColborneMichael Smith Genome Sciences Centre, BC Cancer Agency, Vancouver, Canada.
Gian Luca NegriMichael Smith Genome Sciences Centre, BC Cancer Agency, Vancouver, Canada.ORCID 0000-0001-7722-8888
Friedrich KommossInstitute of Pathology, Medizin Campus Bodensee, Friedrichshafen, Germany.
Anthony KarnezisDepartment of Pathology and Laboratory Medicine, University of California, Davis, California.
Gregg B MorinMichael Smith Genome Sciences Centre, BC Cancer Agency, Vancouver, Canada.ORCID 0000-0001-8949-4374
Jessica N McAlpineDepartment of Obstetrics and Gynecology, University of British Columbia, Vancouver, Canada.ORCID 0000-0001-6003-485X
C Blake GilksDepartment of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, Canada.
Bernard E WeissmanDepartment of Pathology and Laboratory Medicine, UNC-Chapel Hill, Chapel Hill, North Carolina.ORCID 0000-0002-1827-2309
Jeffrey M TrentIntegrated Cancer Genomics, The Translational Genomics Research Institute, Phoenix, Arizona.ORCID 0000-0003-0183-4202
Lynn HoangDepartment of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, Canada.
Patrick PirrotteCollaborative Center for Translational Mass Spectrometry, The Translational Genomics Research Institute, Phoenix, Arizona.ORCID 0000-0003-1360-6039
Yemin WangDepartment of Molecular Oncology, BC Cancer Agency, Vancouver, Canada.
David G HuntsmanDepartment of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, Canada. dhuntsma@bccancer.bc.ca.
University of British Columbia · CABC Cancer Agency · CATranslational Genomics Research Institute · USCentre for Advancing Health Outcomes · CACanada's Michael Smith Genome Sciences Centre · CAMedizin Campus Bodensee · DEUniversity of California, Davis · USUniversity of North Carolina Health Care · US

Funding

Transgenic Mouse FacilityP30CA033572 · NCI · CITY OF HOPE/BECKMAN RESEARCH INSTITUTE · PI STANLEY R. HAMILTON · 1985 to 2026
$86.3M
The Tumor Suppressor Role of SMARCA4 in SCCOHTR01CA195670 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI HUNTSMAN, DAVID, TRENT, JEFFREY M. · 2015 to 2019
$3.7M
CIHR 154290NCI NIH HHS P30 CA033572NCI NIH HHS R01 CA195670
6 · The paper itself

Abstract

purposeMany rare ovarian cancer subtypes, such as small-cell carcinoma of the ovary, hypercalcemic type (SCCOHT), have poor prognosis due to their aggressive nature and resistance to standard platinum- and taxane-based chemotherapy. The development of effective therapeutics has been hindered by the rarity of such tumors. We sought to identify targetable vulnerabilities in rare ovarian cancer subtypes. EXPERIMENTAL

designWe compared the global proteomic landscape of six cases each of endometrioid ovarian cancer (ENOC), clear cell ovarian cancer (CCOC), and SCCOHT to the most common subtype, high-grade serous ovarian cancer (HGSC), to identify potential therapeutic targets. IHC of tissue microarrays was used as validation of arginosuccinate synthase (ASS1) deficiency. The efficacy of arginine-depriving therapeutic ADI-PEG20 was assessed

resultsGlobal proteomic analysis identified low ASS1 expression in ENOC, CCOC, and SCCOHT compared with HGSC. Low ASS1 levels were validated through IHC in large patient cohorts. The lowest levels of ASS1 were observed in SCCOHT, where ASS1 was absent in 12 of 31 cases, and expressed in less than 5% of the tumor cells in 9 of 31 cases. ASS1-deficient ovarian cancer cells were sensitive to ADI-PEG20 treatment regardless of subtype

conclusionsPreclinical

Indexed as

AnimalsArginineArgininosuccinate SynthaseCarcinoma, Small CellCell Line, TumorCell ProliferationFemaleHumansHydrolasesMiceOvarian NeoplasmsOvaryParathyroid Hormone-Related ProteinPolyethylene GlycolsProteomicsXenograft Model Antitumor AssaysADI PEG20ArginineArgininosuccinate SynthaseHydrolasesParathyroid Hormone-Related ProteinPolyethylene Glycols

Identifiers

PMID32409304
PMCPMC7442649
OpenAlexW3025061287

What OpenQuestion holds

Textmetadata
LicenceTDM
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.