Evidence map›Paper›PMID 31205032›Full record

ArticleThe Journal of clinical investigation2019

Preoperative stimulation of resolution and inflammation blockade eradicates micrometastases.

Dipak Panigrahy, Allison Gartung, Jun Yang, Haixia Yang, Molly M Gilligan, Megan L Sulciner, Swati S Bhasin, Diane R Bielenberg, Jaimie Chang, Birgitta A Schmidt and 12 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of clinical investigation, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 77 papers.

0numbers the graph read from it
0cells of the map it votes in
77citing papers in PubMed
13.5field-weighted citation impact, top 1% 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

77 citing papers in PubMed, 136 citations in OpenAlex.

  1. Review
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  7. Metabolic Implications of Efferocytosis During Inflammation.Advances in experimental medicine and biology · 2025
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  13. Multi-stage mechanisms of tumor metastasis and therapeutic strategies.Signal transduction and targeted therapy · 2024
    Review
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  18. Review
  19. Article
  20. Review

17 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

22 authors at 7 institutions in 1 country.

Dipak PanigrahyCenter for Vascular Biology Research.
Allison GartungCenter for Vascular Biology Research.
Jun YangDepartment of Entomology and Nematology, and UC Davis Comprehensive Cancer Center, University of California, Davis, California, USA.
Haixia YangCenter for Vascular Biology Research.
Molly M GilliganCenter for Vascular Biology Research.
Megan L SulcinerCenter for Vascular Biology Research.
Swati S BhasinDivision of Interdisciplinary Medicine and Biotechnology, Department of Medicine, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts, USA.
Diane R BielenbergVascular Biology Program and.
Jaimie ChangCenter for Vascular Biology Research.
Birgitta A SchmidtDepartment of Pathology, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
Julia PiwowarskiCenter for Vascular Biology Research.
Anna FishbeinCenter for Vascular Biology Research.
Dulce Soler-FerranCenter for Vascular Biology Research.
Matthew A SparksDivision of Nephrology, Department of Medicine, Duke University and Durham VA Medical Centers, Durham, North Carolina, USA.
Steven J StaffaDepartment of Anesthesiology, Critical Care and Pain Medicine, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
Vidula SukhatmeGlobalCures Inc., Newton, Massachusetts, USA.
Bruce D HammockDepartment of Entomology and Nematology, and UC Davis Comprehensive Cancer Center, University of California, Davis, California, USA.
Mark W KieranDivision of Pediatric Oncology, Dana-Farber Cancer Institute, and.
Sui HuangInstitute for Systems Biology, Seattle, Washington, USA.
Manoj BhasinDivision of Interdisciplinary Medicine and Biotechnology, Department of Medicine, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts, USA.
Charles N SerhanCenter for Experimental Therapeutics and Reperfusion Injury, Department of Anesthesiology, Perioperative and Pain Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
Vikas P SukhatmeCancer Center, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts, USA.
Beth Israel Deaconess Medical Center · USBoston Children's Hospital · USUniversity of California, Davis · USBrigham and Women's Hospital · USCenter for Vascular Biology Research · USDuke University · USInstitute for Systems Biology · US

Funding

Workshop on Environmental Technology Transfer and EntrepreneurshipP42ES004699 · NIEHS · UNIVERSITY OF CALIFORNIA DAVIS · PI HAMMOCK, BRUCE D · 1987 to 2021
$50.1M
Resolution Mechanisms in Acute Inflammation: Resolution PharmacologyP01GM095467 · NIGMS · BRIGHAM AND WOMEN'S HOSPITAL · PI PETASIS, NICOS A · 2011 to 2020
$14.8M
BLOOD CELL LIPOXYGENASE PRODUCTS: FORMATION AND ACTIONR01GM038765 · NIGMS · BRIGHAM AND WOMEN'S HOSPITAL · PI SERHAN, CHARLES NICHOLAS · 1992 to 2020
$4.9M
HYDROLYTIC ENZYMES IN THE METABOLISM OF TOXINSR01ES002710 · NIEHS · UNIVERSITY OF CALIFORNIA DAVIS · PI HAMMOCK, BRUCE D · 1985 to 2018
$4.0M
Controlling cancer with aspirin-triggered stimulation of resolutionR01CA170549 · NCI · BOSTON CHILDREN'S HOSPITAL · PI PANIGRAHY, DIPAK, SERHAN, CHARLES NICHOLAS · 2012 to 2015
$1.9M
NCI NIH HHS R01 CA170549NIEHS NIH HHS P42 ES004699NIEHS NIH HHS R01 ES002710NIGMS NIH HHS P01 GM095467NIGMS NIH HHS R01 GM038765
6 · The paper itself

Abstract

Cancer therapy is a double-edged sword, as surgery and chemotherapy can induce an inflammatory/immunosuppressive injury response that promotes dormancy escape and tumor recurrence. We hypothesized that these events could be altered by early blockade of the inflammatory cascade and/or by accelerating the resolution of inflammation. Preoperative, but not postoperative, administration of the nonsteroidal antiinflammatory drug ketorolac and/or resolvins, a family of specialized proresolving autacoid mediators, eliminated micrometastases in multiple tumor-resection models, resulting in long-term survival. Ketorolac unleashed anticancer T cell immunity that was augmented by immune checkpoint blockade, negated by adjuvant chemotherapy, and dependent on inhibition of the COX-1/thromboxane A2 (TXA2) pathway. Preoperative stimulation of inflammation resolution via resolvins (RvD2, RvD3, and RvD4) inhibited metastases and induced T cell responses. Ketorolac and resolvins exhibited synergistic antitumor activity and prevented surgery- or chemotherapy-induced dormancy escape. Thus, simultaneously blocking the ensuing proinflammatory response and activating endogenous resolution programs before surgery may eliminate micrometastases and reduce tumor recurrence.

Indexed as

Neoplasms, ExperimentalPreoperative CareAnimalsDocosahexaenoic AcidsImmunity, CellularKetorolacMaleMiceMice, KnockoutNeoplasm MetastasisNeoplasm Recurrence, LocalT-LymphocytesDocosahexaenoic AcidsKetorolacCancerEicosanoidsInflammationOncologySurgery

Identifiers

PMID31205032
PMCPMC6597207
OpenAlexW2949645446

What OpenQuestion holds

Textmetadata
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.