Evidence map›Paper›PMID 35577388›Full record

ArticleLife science alliance2022

The HDL particle composition determines its antitumor activity in pancreatic cancer.

Raimund Oberle, Kristina Kührer, Tamina Österreicher, Florian Weber, Stefanie Steinbauer, Florian Udonta, Mark Wroblewski, Isabel Ben-Batalla, Ingrid Hassl, Jakob Körbelin and 7 more

Open access · goldAbstract read
In one paragraph

Article in Life science alliance, 2022. 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
3.2field-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

17 citing papers in PubMed, 29 citations in OpenAlex.

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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

17 authors at 6 institutions in 3 countries.

Raimund OberleCenter for Pathobiochemistry and Genetics, Medical University of Vienna, Vienna, Austria raimund.oberle@meduniwien.ac.at.ORCID 0000-0001-6701-4130
Kristina KührerCenter for Pathobiochemistry and Genetics, Medical University of Vienna, Vienna, Austria.
Tamina ÖsterreicherCenter for Pathobiochemistry and Genetics, Medical University of Vienna, Vienna, Austria.
Florian WeberSchool of Medical Engineering and Applied Social Sciences, University of Applied Sciences Upper Austria, Linz, Austria.ORCID 0000-0002-8946-1377
Stefanie SteinbauerCenter of Excellence Food Technology and Nutrition, University of Applied Sciences Upper Austria, Wels, Austria.ORCID 0000-0002-2820-5222
Florian UdontaDepartment of Oncology, Hematology and Bone Marrow Transplantation, University Comprehensive Cancer Center Hamburg, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Mark WroblewskiDepartment of Oncology, Hematology and Bone Marrow Transplantation, University Comprehensive Cancer Center Hamburg, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Isabel Ben-BatallaDivision of Personalized Medical Oncology (A420), German Cancer Research Center (DKFZ), Heidelberg, Germany.
Ingrid HasslCenter for Pathobiochemistry and Genetics, Medical University of Vienna, Vienna, Austria.
Jakob KörbelinENDomics Lab, Department of Oncology, Hematology and Bone Marrow Transplantation, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.ORCID 0000-0002-5435-7182
Matthias UnseldDepartment of Medicine I, Division of Palliative Medicine, Medical University of Vienna, Vienna, Austria.
Matti JauhiainenMinerva Foundation Institute for Medical Research and Finnish Institute for Health and Welfare, Genomics and Biobank Unit, Biomedicum 2U, Helsinki, Finland.
Birgit PlochbergerSchool of Medical Engineering and Applied Social Sciences, University of Applied Sciences Upper Austria, Linz, Austria.
Clemens RöhrlCenter of Excellence Food Technology and Nutrition, University of Applied Sciences Upper Austria, Wels, Austria.ORCID 0000-0002-1192-0748
Markus HengstschlägerCenter for Pathobiochemistry and Genetics, Medical University of Vienna, Vienna, Austria.
Sonja LogesDepartment of Personalized Oncology, University Hospital Mannheim, Medical Faculty Mannheim, University of Heidelberg, Mannheim, Germany.ORCID 0000-0002-7650-8527
Herbert StanglCenter for Pathobiochemistry and Genetics, Medical University of Vienna, Vienna, Austria.ORCID 0000-0002-7288-7320
Medical University of Vienna · ATUniversity of Applied Sciences Upper Austria · ATUniversität Hamburg · DEFinnish Institute for Health and Welfare · FIGerman Cancer Research Center · DEHeidelberg University · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite enormous efforts to improve therapeutic options, pancreatic cancer remains a fatal disease and is expected to become the second leading cause of cancer-related deaths in the next decade. Previous research identified lipid metabolic pathways to be highly enriched in pancreatic ductal adenocarcinoma (PDAC) cells. Thereby, cholesterol uptake and synthesis promotes growth advantage to and chemotherapy resistance for PDAC tumor cells. Here, we demonstrate that high-density lipoprotein (HDL)-mediated efficient cholesterol removal from cancer cells results in PDAC cell growth reduction and induction of apoptosis in vitro. This effect is driven by an HDL particle composition-dependent interaction with SR-B1 and ABCA1 on cancer cells. AAV-mediated overexpression of APOA1 and rHDL injections decreased PDAC tumor development in vivo. Interestingly, plasma samples from pancreatic-cancer patients displayed a significantly reduced APOA1-to-SAA1 ratio and a reduced cholesterol efflux capacity compared with healthy donors. We conclude that efficient, HDL-mediated cholesterol depletion represents an interesting strategy to interfere with the aggressive growth characteristics of PDAC.

Indexed as

Carcinoma, Pancreatic DuctalPancreatic NeoplasmsCell ProliferationCholesterolHumansCholesterol

Identifiers

PMID35577388
PMCPMC9112193
OpenAlexW4280504152

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.