Evidence map›Paper›PMID 33491755›Full record

ArticleInternational journal of oncology2021

Effects of PI3K and FGFR inhibitors alone and in combination, and with/without cytostatics in childhood neuroblastoma cell lines.

Stefan Holzhauser, Monika Lukoseviciute, Christina Papachristofi, Christina Vasilopoulou, Nikolas Herold, Malin Wickström, Ourania N Kostopoulou, Tina Dalianis

Open access · bronzeAbstract read
In one paragraph

Article in International journal of oncology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.5field-weighted citation impact, top 9% 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

10 citing papers in PubMed, 24 citations in OpenAlex.

  1. Targeting FGFR for cancer therapy.Journal of hematology & oncology · 2024
    Review
  2. Article
  3. Article
  4. Review
  5. Review
  6. Review
  7. JCO precision oncology · 2022
    Review
  8. Review
  9. Adult adrenal neuroblastoma: A case report.Molecular and clinical oncology · 2021
    Article
  10. Article
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

8 authors at 1 institution in 1 country.

Stefan HolzhauserDepartment of Oncology‑Pathology, Karolinska Institutet, 17164 Stockholm, Sweden.
Monika LukoseviciuteDepartment of Oncology‑Pathology, Karolinska Institutet, 17164 Stockholm, Sweden.
Christina PapachristofiDepartment of Oncology‑Pathology, Karolinska Institutet, 17164 Stockholm, Sweden.
Christina VasilopoulouDepartment of Oncology‑Pathology, Karolinska Institutet, 17164 Stockholm, Sweden.
Nikolas HeroldChildren and Women's Health, Karolinska Institutet, 17164 Stockholm, Sweden.
Malin WickströmChildren and Women's Health, Karolinska Institutet, 17164 Stockholm, Sweden.
Ourania N Kostopoulou *Department of Oncology‑Pathology, Karolinska Institutet, 17164 Stockholm, Sweden.
Tina Dalianis *Department of Oncology‑Pathology, Karolinska Institutet, 17164 Stockholm, Sweden.
Karolinska Institutet · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Neuroblastoma (NB) is a heterogenous disease with treatment varying from observation for low‑risk tumors, to extensive therapy with chemotherapy, surgery, radiotherapy, and autologous bone‑marrow‑transplantation and immunotherapy. However, a high frequency of primary‑chemo‑refractory disease and recurrences urgently require novel treatment strategies. The present study therefore investigated the anti‑NB efficacy of the recently FDA‑approved phosphoinositide 3‑kinase (PI3K) and fibroblast growth factor receptor (FGFR) inhibitors, alpelisib (BYL719) and erdafitinib (JNJ‑42756493), alone and in combination with or without cisplatin, vincristine, or doxorubicin on 5 NB cell lines. For this purpose, the NB cell lines, SK‑N‑AS, SK‑N‑BE(2)‑C, SK‑N‑DZ, SK‑N‑FI and SK‑N‑SH (where SK‑N‑DZ had a deletion of PIK3C2G and none had FGFR mutations according to the Cancer Program's Dependency Map, although some were chemoresistant), were tested for their sensitivity to FDA‑approved inhibitors alone or in combination, or together with cytostatic drugs by viability, cytotoxicity, apoptosis and proliferation assays. The results revealed that monotherapy with alpelisib or erdafitinib resulted in a dose‑dependent inhibition of cell viability and proliferation. Notably, the combined use of PI3K and FGFR inhibitors resulted in an enhanced efficacy, while their combined use with the canonical cytotoxic agents, cisplatin, vincristine and doxorubicin, resulted in variable synergistic, additive and antagonistic effects. Collectively, the present study provides pre‑clinical evidence that PI3K and FGFR inhibitors exhibit promising anti‑NB activity. The data presented herein also indicate that the incorporation of these inhibitors into chemotherapeutic regimens requires careful consideration and further research in order to obtain a beneficial efficacy. Nevertheless, the addition of PI3K and FGFR inhibitors to the treatment arsenal might reduce the occurrence of refractory and relapsing disease in NB without FGFR and PI3K mutations.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsApoptosisCell Line, TumorCell ProliferationCell SurvivalChildCisplatinCytostatic AgentsDoxorubicinDrug Resistance, NeoplasmDrug SynergismHumansNeuroblastomaPhosphoinositide-3 Kinase InhibitorsPyrazolesQuinoxalinesAlpelisibCisplatinCytostatic AgentsDoxorubicinerdafitinibPhosphoinositide-3 Kinase InhibitorsPyrazolesQuinoxalinesReceptors, Fibroblast Growth FactorThiazolesVincristineBYL719chemotherapycisplatindoxorubicinFGFR inhibitorsJNJ‑42756493neuroblastomaPI3K inhibitorsvincristine

Identifiers

PMID33491755
PMCPMC7864013
OpenAlexW3120283294

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.