Evidence map›Paper›PMID 25603975›Full record

ArticleInvestigational new drugs2015

Treatment effect of buparlisib, cetuximab and irradiation in wild-type or PI3KCA-mutated head and neck cancer cell lines.

Laura Lattanzio, Federica Tonissi, Martino Monteverde, Daniela Vivenza, Elvio Russi, Gérard Milano, Marco Merlano, Cristiana Lo Nigro

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Article in Investigational new drugs, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

18 citing papers in PubMed, 37 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

8 authors at 2 institutions in 2 countries.

Laura LattanzioLaboratory of Cancer Genetics and Translational Oncology, Oncology Department, S. Croce University Hospital, Via Carle 25, 12100, Cuneo, Italy.
Federica Tonissi
Martino Monteverde
Daniela Vivenza
Elvio Russi
Gérard Milano
Marco Merlano
Cristiana Lo Nigro
Azienda Sanitaria Ospedaliera S.Croce e Carle Cuneo · ITCentre Antoine Lacassagne · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction In complement to anti-EGFR therapy, the targeting of PI3K/AKT/mTOR signaling pathway is of particular interest in the management of Head and Neck Squamous Cell Carcinoma (HNSCC). Here, we assess the effects of PI3K inhibition combined with anti-EGFR monoclonal antibody cetuximab and/or irradiation (RT). Material and methods Anti-proliferative effects of the combination of buparlisib (a specific PI3K inhibitor), cetuximab and RT was determined in two HNSCC cell lines (CAL33, PI3KCA H1047R-mutated and CAL27, PI3KCA wild-type). We examined biochemical factors related to proliferation, apoptosis (caspases), DNA repair (ERCC1, XRCC1) and the PI3K pathway (pEGFR/EGFR, pAKT/AKT, p-p70, p4EBP1). Results The best synergistic combined treatment in inhibiting cell proliferation was sequence 2 (cetuximab followed by buparlisib) in both cell lines. Addition of RT increased sequence 2 anti-proliferative effect only in CAL27. Data on protein expression indicated a possible activation of mTORC2 complex and caspases proteins in CAL27 not seen in CAL33. In CAL33, the synergistic anti-proliferative effect of the two drugs may derive from the higher sensitivity of mutated cells to PI3K targeting. Conclusions Our study demonstrates a synergistic effect of cetuximab followed by buparlisib in both PI3KCA wild-type and mutated cells, even with different intracellular signaling cross-talk depending on mutational status.

Indexed as

AminopyridinesAntineoplastic AgentsApoptosisCell Line, TumorCell ProliferationCetuximabChemoradiotherapyDNA RepairDrug Resistance, NeoplasmErbB ReceptorsHead and Neck NeoplasmsHumansMechanistic Target of Rapamycin Complex 2MorpholinesMultiprotein ComplexesPhosphatidylinositol 3-KinasesAminopyridinesAntineoplastic AgentsCetuximabErbB ReceptorsMechanistic Target of Rapamycin Complex 2MorpholinesMTOR protein, humanMultiprotein ComplexesNVP-BKM120Phosphatidylinositol 3-KinasesTOR Serine-Threonine Kinases

Identifiers

PMID25603975
OpenAlexW2042288129

What Socratic holds

Textmetadata
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 Socratic graph.