Evidence map›Paper›PMID 33093149›Full record

Observational studyClinical cancer research : an official journal of the American Association for Cancer Research2021

Detection of Chemotherapy-resistant Pancreatic Cancer Using a Glycan Biomarker, sTRA.

ChongFeng Gao, Luke Wisniewski, Ying Liu, Ben Staal, Ian Beddows, Dennis Plenker, Mohammed Aldakkak, Johnathan Hall, Daniel Barnett, Mirna Kheir Gouda and 10 more

Open access · greenAbstract readObservational Study
In one paragraph

Observational study in Clinical cancer research : an official journal of the American Association for Cancer Research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.5field-weighted citation impact, top 15% 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

17 citing papers in PubMed, 28 citations in OpenAlex.

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  12. Selective ablation of TRA-1-60Theranostics · 2023
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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

20 authors at 7 institutions in 1 country.

ChongFeng GaoCenter for Cancer and Cell Biology, Van Andel Institute, Grand Rapids, Michigan.
Luke WisniewskiCenter for Cancer and Cell Biology, Van Andel Institute, Grand Rapids, Michigan.ORCID 0000-0003-1905-4992
Ying LiuCenter for Cancer and Cell Biology, Van Andel Institute, Grand Rapids, Michigan.
Ben StaalCenter for Cancer and Cell Biology, Van Andel Institute, Grand Rapids, Michigan.
Ian BeddowsCenter for Cancer and Cell Biology, Van Andel Institute, Grand Rapids, Michigan.
Dennis PlenkerLustgarten Foundation Pancreatic Cancer Research Laboratory, Cold Spring Harbor Laboratory, Cold Spring Harbor, New York.ORCID 0000-0003-3895-4064
Mohammed AldakkakDepartment of Surgery, Medical College of Wisconsin, Milwaukee, Wisconsin.
Johnathan HallCenter for Cancer and Cell Biology, Van Andel Institute, Grand Rapids, Michigan.
Daniel BarnettCenter for Cancer and Cell Biology, Van Andel Institute, Grand Rapids, Michigan.ORCID 0000-0003-3512-3329
Mirna Kheir GoudaLustgarten Foundation Pancreatic Cancer Research Laboratory, Cold Spring Harbor Laboratory, Cold Spring Harbor, New York.
Peter AllenDivision of Surgical Oncology, Duke University School of Medicine, Durham, North Carolina.
Richard DrakeCell and Molecular Pharmacology and Experimental Therapeutics, Medical University of South Carolina, Charleston, South Carolina.
Amer ZureikatDivision of Gastrointestinal Surgical Oncology, University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania.
Ying HuangDivision of Vaccine and Infectious Disease, Fred Hutchinson Cancer Research Center, Seattle, Washington.ORCID 0000-0002-9655-7502
Douglas EvansDepartment of Surgery, Medical College of Wisconsin, Milwaukee, Wisconsin.ORCID 0000-0001-5708-467X
Aatur SinghiDivision of Gastrointestinal Surgical Oncology, University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania.
Randall E BrandDivision of Gastrointestinal Surgical Oncology, University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania.ORCID 0000-0002-4136-3313
David A TuvesonLustgarten Foundation Pancreatic Cancer Research Laboratory, Cold Spring Harbor Laboratory, Cold Spring Harbor, New York.
Susan TsaiDepartment of Surgery, Medical College of Wisconsin, Milwaukee, Wisconsin.
Brian B HaabCenter for Cancer and Cell Biology, Van Andel Institute, Grand Rapids, Michigan. brian.haab@vai.org.
Van Andel Institute · USCold Spring Harbor Laboratory · USMedical College of Wisconsin · USUniversity of Pittsburgh Medical Center · USDuke University · USInfectious Disease Research Institute · USMedical University of South Carolina · US

Funding

Single-Cell Biology Shared ResourceP30CA045508 · NCI · COLD SPRING HARBOR LABORATORY · PI John Edward Moses · 1987 to 2026
$118.9M
The Early Detection Research Network: Data Management and Coordinating CenterU24CA086368 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI RUTH D ETZIONI, Ziding Feng · 2010 to 2026
$75.7M
Detection of Pre-Invasive Pancreatic Cysts Using Protein and Glycan BiomarkersU01CA152653 · NCI · VAN ANDEL RESEARCH INSTITUTE · PI ALLEN, PETER J, BRAND, RANDALL · 2010 to 2021
$5.8M
Subpopulations of Pancreatic Cancer Cells Defined by Glycan MarkersU01CA226158 · NCI · VAN ANDEL RESEARCH INSTITUTE · PI BRAND, RANDALL, HAAB, BRIAN B. · 2019 to 2023
$3.2M
NCI NIH HHS P30 CA045508NCI NIH HHS U01 CA152653NCI NIH HHS U01 CA226158NCI NIH HHS U24 CA086368
6 · The paper itself

Abstract

purposeA subset of pancreatic ductal adenocarcinomas (PDACs) is highly resistant to systemic chemotherapy, but no markers are available in clinical settings to identify this subset. We hypothesized that a glycan biomarker for PDACs called sialylated tumor-related antigen (sTRA) could be used for this purpose. EXPERIMENTAL

designWe tested for differences between PDACs classified by glycan expression in multiple systems: sets of cell lines, organoids, and isogenic cell lines; primary tumors; and blood plasma from human subjects.

resultsThe sTRA-expressing models tended to have stem-like gene expression and the capacity for mesenchymal differentiation, in contrast to the nonexpressing models. The sTRA cell lines also had significantly increased resistance to seven different chemotherapeutics commonly used against pancreatic cancer. Patients with primary tumors that were positive for a gene expression classifier for sTRA received no statistically significant benefit from adjuvant chemotherapy, in contrast to those negative for the signature. In another cohort, based on direct measurements of sTRA in tissue microarrays, the patients who were high in sTRA again had no statistically significant benefit from adjuvant chemotherapy. Furthermore, a blood plasma test for the sTRA glycan identified the PDACs that showed rapid relapse following neoadjuvant chemotherapy.

conclusionsThis research demonstrates that a glycan biomarker could have value to detect chemotherapy-resistant PDAC in clinical settings. This capability could aid in the development of stratified treatment plans and facilitate biomarker-guided trials targeting resistant PDAC.

Indexed as

Antigens, Tumor-Associated, CarbohydrateAntineoplastic AgentsBiomarkers, TumorCarcinoma, Pancreatic DuctalCell Line, TumorDisease-Free SurvivalDrug Resistance, NeoplasmHumansInhibitory Concentration 50Liquid BiopsyNeoplasm Recurrence, LocalPancreatic NeoplasmsPolysaccharidesRisk AssessmentAntigens, Tumor-Associated, CarbohydrateAntineoplastic AgentsBiomarkers, TumorPolysaccharides

Identifiers

PMID33093149
PMCPMC7785673
OpenAlexW3093581336

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.