Evidence map›Paper›PMID 36225637›Full record

ArticleAmerican journal of cancer research2022

Treatment effects of the EGFR pathway drugs on head and neck cancer stem cells.

Glaucia Maria de Mendonça Fernandes, Vilson Serafim Junior, Ana Lívia Silva Galbiatti-Dias, Leticia Antunes Muniz Ferreira, Márcia Maria Urbanin Castanhole-Nunes, Rosa Sayoko Kawasaki-Oyama, José Victor Maniglia, Erika Cristina Pavarino, Eny Maria Goloni-Bertollo

Open access · greenAbstract read
In one paragraph

Article in American journal of cancer research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.6field-weighted citation impact, top 38% 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

5 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. 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

9 authors at 1 institution in 1 country.

Glaucia Maria de Mendonça FernandesMolecular Biology Department, Genetics and Molecular Biology Research Unit (UPGEM), Faculdade de Medicina de São José do Rio Preto (FAMERP) São José do Rio Preto, São Paulo, Brazil.
Vilson Serafim JuniorMolecular Biology Department, Genetics and Molecular Biology Research Unit (UPGEM), Faculdade de Medicina de São José do Rio Preto (FAMERP) São José do Rio Preto, São Paulo, Brazil.
Ana Lívia Silva Galbiatti-DiasMolecular Biology Department, Genetics and Molecular Biology Research Unit (UPGEM), Faculdade de Medicina de São José do Rio Preto (FAMERP) São José do Rio Preto, São Paulo, Brazil.
Leticia Antunes Muniz FerreiraMolecular Biology Department, Genetics and Molecular Biology Research Unit (UPGEM), Faculdade de Medicina de São José do Rio Preto (FAMERP) São José do Rio Preto, São Paulo, Brazil.
Márcia Maria Urbanin Castanhole-NunesMolecular Biology Department, Genetics and Molecular Biology Research Unit (UPGEM), Faculdade de Medicina de São José do Rio Preto (FAMERP) São José do Rio Preto, São Paulo, Brazil.
Rosa Sayoko Kawasaki-OyamaMolecular Biology Department, Genetics and Molecular Biology Research Unit (UPGEM), Faculdade de Medicina de São José do Rio Preto (FAMERP) São José do Rio Preto, São Paulo, Brazil.
José Victor ManigliaDepartment of Otolaryngology and Head and Neck Surgery, Faculdade de Medicina de São José do Rio Preto (FAMERP) São José do Rio Preto, São Paulo, Brazil.
Erika Cristina PavarinoMolecular Biology Department, Genetics and Molecular Biology Research Unit (UPGEM), Faculdade de Medicina de São José do Rio Preto (FAMERP) São José do Rio Preto, São Paulo, Brazil.
Eny Maria Goloni-BertolloMolecular Biology Department, Genetics and Molecular Biology Research Unit (UPGEM), Faculdade de Medicina de São José do Rio Preto (FAMERP) São José do Rio Preto, São Paulo, Brazil.
Faculdade de Medicina de São José do Rio Preto · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

(1) Head and neck cancer (HNC) is the sixth most common cancer worldwide and show low survival rates and drug resistance, which can be due to the presence of cancer stem cells (CSCs), a small cell population with metastatic potential, invasion and self-renewal ability. (2) Here, seven tumor cells were sorted as CD44+/CD117+/CD133+ or ALDH+, considered as HNC stem cells (HNCSCs), and as CD44-/CD117-/CD133- or ALDH-, considered non-HNCSCs after both cells sorted criteria was compared to evaluate cell migration, invasion, and colony forming assays. These subpopulations were treated with Cetuximab, Paclitaxel, or a combination of both drugs and evaluated for cell viability. Quantitative PCR and western blot were performed to evaluate EGFR, TRKB, KRAS and HIF-1α gene and protein expression. (3) HNCSCs presented more colonies and appeared to be more sensitive to the drug combination when compared with non-HNCSCs, regardless cells sorted criteria and primary tumor subsite. The EGFR, TRKB, KRAS and HIF-1α genes and proteins were upregulated in CSCs compared with non-HNCSCs, thus explaining the drug resistance. (4) This study contributes to the better development of specific therapeutic protocols based on Cetuximab and Paclitaxel drugs in the treatment of HNC in the presence of CSCs and cell proliferation biomarkers.

Indexed as

cancer stem cellscetuximabepidermal growth factor receptorHead and neck cancerKirsten sarcoma ratpaclitaxel

Identifiers

PMID36225637
PMCPMC9548020
OpenAlexW4306167787

What OpenQuestion 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 OpenQuestion graph.