Evidence map›Paper›PMID 30982764›Full record

ArticleEBioMedicine2019

Quantitative proteomics identifies brain acid soluble protein 1 (BASP1) as a prognostic biomarker candidate in pancreatic cancer tissue.

Qimin Zhou, Roland Andersson, Dingyuan Hu, Monika Bauden, Theresa Kristl, Agata Sasor, Krzysztof Pawłowski, Indira Pla, Katarzyna Said Hilmersson, Mengtao Zhou and 3 more

Open access · goldAbstract read
In one paragraph

Article in EBioMedicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
3.5field-weighted citation impact, top 6% 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

37 citing papers in PubMed, 64 citations in OpenAlex.

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  13. Proteomics techniques in protein biomarker discovery.Quantitative biology (Beijing, China) · 2024
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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

13 authors at 4 institutions in 3 countries.

Qimin ZhouDepartment of Surgery, Clinical Sciences Lund, Lund University and Skåne University Hospital, Lund, Sweden; The Eye Hospital, School of Ophthalmology and Optometry, Wenzhou Medical University, Wenzhou, Zhejiang, China; Key Laboratory of Diagnosis and Treatment of Severe Hepato-Pancreatic Diseases of Zhejiang Province, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.
Roland AnderssonDepartment of Surgery, Clinical Sciences Lund, Lund University and Skåne University Hospital, Lund, Sweden.
Dingyuan HuDepartment of Surgery, Clinical Sciences Lund, Lund University and Skåne University Hospital, Lund, Sweden.
Monika BaudenDepartment of Surgery, Clinical Sciences Lund, Lund University and Skåne University Hospital, Lund, Sweden.
Theresa KristlDepartment of Surgery, Clinical Sciences Lund, Lund University and Skåne University Hospital, Lund, Sweden.
Agata SasorDepartment of Pathology, Skåne University Hospital, Lund, Sweden.
Krzysztof PawłowskiDepartment of Experimental Design and Bioinformatics, Warsaw University of Life Sciences, Warsaw, Poland; Department of Translational Medicine, Lund University, Malmö, Sweden.
Indira PlaDepartment of Biomedical Engineering, Clinical Protein Science and Imaging, Lund University, Lund, Sweden.
Katarzyna Said HilmerssonDepartment of Surgery, Clinical Sciences Lund, Lund University and Skåne University Hospital, Lund, Sweden.
Mengtao ZhouKey Laboratory of Diagnosis and Treatment of Severe Hepato-Pancreatic Diseases of Zhejiang Province, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.
Fan LuThe Eye Hospital, School of Ophthalmology and Optometry, Wenzhou Medical University, Wenzhou, Zhejiang, China.
György Marko-VargaDepartment of Biomedical Engineering, Clinical Protein Science and Imaging, Lund University, Lund, Sweden.
Daniel AnsariDepartment of Surgery, Clinical Sciences Lund, Lund University and Skåne University Hospital, Lund, Sweden. Electronic address: daniel.ansari@med.lu.se.
Lund University · SEWenzhou Medical University · CNSkåne University Hospital · SEWarsaw University of Life Sciences · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPancreatic cancer is a heterogenous disease with a poor prognosis. This study aimed to discover and validate prognostic tissue biomarkers in pancreatic cancer using a mass spectrometry (MS) based proteomics approach.

methodsGlobal protein sequencing of fresh frozen pancreatic cancer and healthy pancreas tissue samples was conducted by MS to discover potential protein biomarkers. Selected candidate proteins were further verified by targeted proteomics using parallel reaction monitoring (PRM). The expression of biomarker candidates was validated by immunohistochemistry in a large tissue microarray (TMA) cohort of 141 patients with resectable pancreatic cancer. Kaplan-Meier and Cox proportional hazard modelling was used to investigate the prognostic utility of candidate protein markers.

findingsIn the initial MS-discovery phase, 165 proteins were identified as potential biomarkers. In the subsequent MS-verification phase, a panel of 45 candidate proteins was verified by the development of a PRM assay. Brain acid soluble protein 1 (BASP1) was identified as a new biomarker candidate for pancreatic cancer possessing largely unknown biological and clinical functions and was selected for further analysis. Importantly, bioinformatic analysis indicated that BASP1 interacts with Wilms tumour protein (WT1) in pancreatic cancer. TMA-based immunohistochemistry analysis showed that BASP1 was an independent predictor of prolonged survival (HR 0.468, 95% CI 0.257-0.852, p = .013) and predicted favourable response to adjuvant chemotherapy, whereas WT1 indicated a worsened survival (HR 1.636, 95% CI 1.083-2.473, p = .019) and resistance to chemotherapy. Interaction analysis showed that patients with negative BASP1 and high WT1 expression had the poorest outcome (HR 3.536, 95% CI 1.336-9.362, p = .011).

interpretationWe here describe an MS-based proteomics platform for developing biomarkers for pancreatic cancer. Bioinformatic analysis and clinical data from our study suggest that BASP1 and its putative interaction partner WT1 can be used as biomarkers for predicting outcomes in pancreatic cancer patients.

Indexed as

Biomarkers, TumorAgedAged, 80 and overChromatography, LiquidComputational BiologyFemaleHumansKaplan-Meier EstimateMaleMembrane ProteinsMiddle AgedNeoplasm MetastasisNeoplasm StagingNerve Tissue ProteinsPancreatic NeoplasmsPrognosisBASP1 protein, humanBiomarkers, TumorMembrane ProteinsNerve Tissue ProteinsProteomeRepressor ProteinsBASP1BiomarkersChemotherapy responseMass spectrometryPancreatic cancerPrognosisWT1

Identifiers

PMID30982764
PMCPMC6557784
OpenAlexW2939523644

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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.