Evidence map›Paper›PMID 30745580›Full record

ArticleBritish journal of cancer2019

Drug sensitivity testing on patient-derived sarcoma cells predicts patient response to treatment and identifies c-Sarc inhibitors as active drugs for translocation sarcomas.

Bertha A Brodin, Krister Wennerberg, Elisabet Lidbrink, Otte Brosjö, Swapnil Potdar, Jennifer N Wilson, Limin Ma, Lotte N Moens, Asle Hesla, Edvin Porovic and 9 more

Open access · hybridAbstract readCase Reports
In one paragraph

Article in British journal of cancer, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
4.2field-weighted citation impact, top 5% 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

26 citing papers in PubMed, 37 citations in OpenAlex.

  1. Drug sensitivity testing of patient-derived bone sarcomas identifies selective kinase inhibitors for patients with refractory disease.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    Article
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  3. Pan-cancer ex vivo target evaluation of phosphodiesterase 3 A (PDE3A).Journal of molecular medicine (Berlin, Germany) · 2026
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  10. Identification ofTranslational cancer research · 2023
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  18. Review
  19. Annual review of cancer biology · 2021
    Article
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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

19 authors at 5 institutions in 3 countries.

Bertha A BrodinDepartment of Microbiology Tumor and Cell Biology (MTC), Karolinska Institutet, Stockholm, Sweden. bertha.brodin@ki.se.
Krister WennerbergInstitute for Molecular Medicine Finland (FIMM), University of Helsinki, Helsinki, Finland.
Elisabet LidbrinkDepartment of Breast cancer, Endocrine tumors and Sarcoma, Karolinska University Hospital, Stockholm, Sweden.
Otte BrosjöDepartment of Tumor Orthopedics, Karolinska University Hospital, Stockholm, Sweden.
Swapnil PotdarInstitute for Molecular Medicine Finland (FIMM), University of Helsinki, Helsinki, Finland.
Jennifer N WilsonDepartment of Microbiology Tumor and Cell Biology (MTC), Karolinska Institutet, Stockholm, Sweden.
Limin MaDepartment of Microbiology Tumor and Cell Biology (MTC), Karolinska Institutet, Stockholm, Sweden.
Lotte N MoensDepartment of Immunology, Genetics and Pathology, Uppsala University, Uppsala, Sweden.
Asle HeslaDepartment of Tumor Orthopedics, Karolinska University Hospital, Stockholm, Sweden.
Edvin PorovicDepartment of Microbiology Tumor and Cell Biology (MTC), Karolinska Institutet, Stockholm, Sweden.
Edvin BernhardssonDepartment of Microbiology Tumor and Cell Biology (MTC), Karolinska Institutet, Stockholm, Sweden.
Antroula PapakonstantinouDepartment of Breast cancer, Endocrine tumors and Sarcoma, Karolinska University Hospital, Stockholm, Sweden.
Henrik BauerDepartment of Tumor Orthopedics, Karolinska University Hospital, Stockholm, Sweden.
Panagiotis TsagkozisDepartment of Tumor Orthopedics, Karolinska University Hospital, Stockholm, Sweden.
Karin von SiversDepartment of Radiology, Karolinska University Hospital, Stockholm, Sweden.
Johan WejdeDepartment of Cytology and Pathology, Karolinska University Hospital, Stockholm, Sweden.
Päivi ÖstlingDepartment of Oncology - Pathology, Karolinska Institutet, Stockholm, Sweden.
Olli KallioniemiDepartment of Oncology - Pathology, Karolinska Institutet, Stockholm, Sweden.
Christina Linder StragliottoDepartment of Breast cancer, Endocrine tumors and Sarcoma, Karolinska University Hospital, Stockholm, Sweden. christina.linder-stragliotto@sll.se.
Karolinska Institutet · SEKarolinska University Hospital · SEInstitute for Molecular Medicine Finland · FIUniversity of Helsinki · FIUppsala University · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHeterogeneity and low incidence comprise the biggest challenge in sarcoma diagnosis and treatment. Chemotherapy, although efficient for some sarcoma subtypes, generally results in poor clinical responses and is mostly recommended for advanced disease. Specific genomic aberrations have been identified in some sarcoma subtypes but few of them can be targeted with approved drugs.

methodsWe cultured and characterised patient-derived sarcoma cells and evaluated their sensitivity to 525 anti-cancer agents including both approved and non-approved drugs. In total, 14 sarcomas and 5 healthy mesenchymal primary cell cultures were studied. The sarcoma biopsies and derived cells were characterised by gene panel sequencing, cancer driver gene expression and by detecting specific fusion oncoproteins in situ in sarcomas with translocations.

resultsSoft tissue sarcoma cultures were established from patient biopsies with a success rate of 58%. The genomic profile and drug sensitivity testing on these samples helped to identify targeted inhibitors active on sarcomas. The cSrc inhibitor Dasatinib was identified as an active drug in sarcomas carrying chromosomal translocations. The drug sensitivity of the patient sarcoma cells ex vivo correlated with the response to the former treatment of the patient.

conclusionsOur results show that patient-derived sarcoma cells cultured in vitro are relevant and practical models for genotypic and phenotypic screens aiming to identify efficient drugs to treat sarcoma patients with poor treatment options.

Indexed as

AdultCell Line, TumorCSK Tyrosine-Protein KinaseDrug Resistance, NeoplasmFemaleHumansMaleSarcomasrc-Family KinasesCSK protein, humanCSK Tyrosine-Protein Kinasesrc-Family Kinases

Identifiers

PMID30745580
PMCPMC6462037
OpenAlexW2912102458

What OpenQuestion holds

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LicenceCC BY
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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.