Evidence map›Paper›PMID 28468237›Full record

ArticleInternational journal of molecular sciences2017

Hypoxia Mediates Differential Response to Anti-EGFR Therapy in HNSCC Cells.

Emilia Wiechec, Katharina Tiefenböck Hansson, Lisa Alexandersson, Jan-Ingvar Jönsson, Karin Roberg

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
1.4field-weighted citation impact, top 21% 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, 1 synthesis or guideline pooled it, 29 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Review
  12. Anti-EGFR treatment effects on laryngeal cancer stem cells.American journal of translational research · 2021
    Article
  13. Oncology letters · 2019
    Article
  14. Cancer biotherapy & radiopharmaceuticals · 2019
    Article
  15. Article
  16. Article
  17. Tumor microenvironment - Unknown niche with powerful therapeutic potential.Reports of practical oncology and radiotherapy : journal of Greatpoland Cancer Center in Poznan and Polish Society of Radiation Oncology
    Review
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

5 authors at 1 institution in 1 country.

Emilia WiechecDepartment of Clinical and Experimental Medicine, Division of Cell Biology, Linköping University, Linköping 581 85, Sweden. emilia.wiechec@liu.se.
Katharina Tiefenböck HanssonDepartment of ENT-Head and Neck Surgery, County Council of Östergötland, Linköping 581 85, Sweden. katharina.tiefenbock@regionostergotland.se.
Lisa AlexanderssonDepartment of ENT-Head and Neck Surgery, County Council of Östergötland, Linköping 581 85, Sweden. lisa.alexandersson@regionostergotland.se.
Jan-Ingvar JönssonDepartment of Clinical and Experimental Medicine, Division of Cell Biology, Linköping University, Linköping 581 85, Sweden. jan-ingvar.jonsson@liu.se.
Karin RobergDepartment of Clinical and Experimental Medicine, Division of Cell Biology, Linköping University, Linköping 581 85, Sweden. karin.roberg@liu.se.
Linköping University · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite advances in the head and neck squamous cell carcinoma (HNSCC) treatment modalities, drug resistance and cancer recurrence are often reported. Hypoxia signaling through hypoxia-inducible factor 1 (HIF-1) promotes angiogenesis and metastasis by inducing epithelial-mesenchymal-transition (EMT). The aim of this study was to evaluate the impact of hypoxia on response to therapy as well as EMT and expression of stem cell markers in HNSCC cells. Five HNSCC cell lines (UT-SCC-2, UT-SCC-14, LK0412, LK0827, and LK0923) were selected for this study. The treatment sensitivity for radiation, cisplatin, cetuximab, and dasatinib was assessed by crystal violet assay. Gene expression of EMT and cancer stem cell (CSC) markers as well as protein level of EGFR signaling molecules were analyzed by qPCR and western blotting, respectively. Unlike UT-SCC-14 and LK0827, the LK0412 cell line became significantly more sensitive to cetuximab in hypoxic conditions. This cetuximab sensitivity was efficiently reversed after suppression of HIF-1α with siRNA. Additionally, hypoxia-induced EMT and expression of stem cell markers in HNSCC cells was partially revoked by treatment with cetuximab or knockdown of HIF-1α. In summary, our study shows that hypoxia might have a positive influence on the anti-EGFR therapy effectiveness in HNSCC. However, due to heterogeneity of HNSCC lesions, targeting HIF-1α may not be sufficient to mediate such a response. Further studies identifying a trait of hypoxia-specific response to cetuximab in HNSCC are advisable.

Indexed as

Antineoplastic Agents, ImmunologicalCarcinoma, Squamous CellCell Line, TumorCetuximabCisplatinDasatinibEpithelial-Mesenchymal TransitionErbB ReceptorsHead and Neck NeoplasmsHumansHypoxiaHypoxia-Inducible Factor 1, alpha SubunitNeoplastic Stem CellsProtein Kinase InhibitorsSignal TransductionSquamous Cell Carcinoma of Head and NeckAntineoplastic Agents, ImmunologicalCetuximabCisplatinDasatinibErbB ReceptorsHypoxia-Inducible Factor 1, alpha SubunitProtein Kinase Inhibitorscancer stem cells (CSC)cetuximabcisplatinepithelial-mesenchymal transition (EMT)head and neck tumorsHIF-1αhypoxiaradiotherapy

Identifiers

PMID28468237
PMCPMC5454856
OpenAlexW2610225152

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.