Evidence map›Paper›PMID 38565739›Full record

ArticleHuman cell2024

Establishment and molecular characterization of HCB-541, a novel and aggressive human cutaneous squamous cell carcinoma cell line.

Ana Carolina Laus, Izabela Natalia Faria Gomes, Aline Larissa Virginio da Silva, Luciane Sussuchi da Silva, Mirella Baroni Milan, Silvia AparecidaTeixeira, Ana Carolina Baptista Moreno Martin, Letícia do Nascimento Braga Pereira, Carlos Eduardo Barbosa de Carvalho, Camila Souza Crovador and 6 more

Open access · hybridAbstract read
In one paragraph

Article in Human cell, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.2field-weighted citation impact, top 22% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. 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

16 authors at 2 institutions in 2 countries.

Ana Carolina LausMolecular Oncology Research Center, Barretos Cancer Hospital, Antenor Duarte Villela, 1331, Barretos, São Paulo, Zip Code: 14784 400, Brazil.ORCID http://orcid.org/0000-0003-4748-8819
Izabela Natalia Faria GomesMolecular Oncology Research Center, Barretos Cancer Hospital, Antenor Duarte Villela, 1331, Barretos, São Paulo, Zip Code: 14784 400, Brazil.ORCID http://orcid.org/0000-0003-0551-138X
Aline Larissa Virginio da SilvaMolecular Oncology Research Center, Barretos Cancer Hospital, Antenor Duarte Villela, 1331, Barretos, São Paulo, Zip Code: 14784 400, Brazil.ORCID http://orcid.org/0000-0003-3260-0847
Luciane Sussuchi da SilvaMolecular Oncology Research Center, Barretos Cancer Hospital, Antenor Duarte Villela, 1331, Barretos, São Paulo, Zip Code: 14784 400, Brazil.ORCID http://orcid.org/0000-0002-7470-4655
Mirella Baroni MilanMolecular Oncology Research Center, Barretos Cancer Hospital, Antenor Duarte Villela, 1331, Barretos, São Paulo, Zip Code: 14784 400, Brazil.ORCID http://orcid.org/0000-0002-1622-9606
Silvia AparecidaTeixeiraMolecular Oncology Research Center, Barretos Cancer Hospital, Antenor Duarte Villela, 1331, Barretos, São Paulo, Zip Code: 14784 400, Brazil.ORCID http://orcid.org/0000-0002-2462-8535
Ana Carolina Baptista Moreno MartinMolecular Oncology Research Center, Barretos Cancer Hospital, Antenor Duarte Villela, 1331, Barretos, São Paulo, Zip Code: 14784 400, Brazil.ORCID http://orcid.org/0000-0001-5426-2223
Letícia do Nascimento Braga PereiraMolecular Oncology Research Center, Barretos Cancer Hospital, Antenor Duarte Villela, 1331, Barretos, São Paulo, Zip Code: 14784 400, Brazil.ORCID http://orcid.org/0000-0003-0874-6600
Carlos Eduardo Barbosa de CarvalhoDepartment of Surgery of Melanoma and Sarcoma, Barretos Cancer Hospital, São Paulo, Brazil.ORCID http://orcid.org/0009-0005-6041-8307
Camila Souza CrovadorDepartment of Surgery of Melanoma and Sarcoma, Barretos Cancer Hospital, São Paulo, Brazil.ORCID http://orcid.org/0000-0002-3604-7033
Flávia Escremin de PaulaMolecular Oncology Research Center, Barretos Cancer Hospital, Antenor Duarte Villela, 1331, Barretos, São Paulo, Zip Code: 14784 400, Brazil.ORCID http://orcid.org/0009-0001-9236-990X
Flávia Caroline NascimentoMolecular Oncology Research Center, Barretos Cancer Hospital, Antenor Duarte Villela, 1331, Barretos, São Paulo, Zip Code: 14784 400, Brazil.ORCID http://orcid.org/0000-0001-8717-8968
Helder Teixeira de FreitasMolecular Oncology Research Center, Barretos Cancer Hospital, Antenor Duarte Villela, 1331, Barretos, São Paulo, Zip Code: 14784 400, Brazil.ORCID http://orcid.org/0000-0002-5885-5322
Vinicius de Lima VazquezMolecular Oncology Research Center, Barretos Cancer Hospital, Antenor Duarte Villela, 1331, Barretos, São Paulo, Zip Code: 14784 400, Brazil.ORCID http://orcid.org/0000-0002-0325-5514
Rui Manuel ReisMolecular Oncology Research Center, Barretos Cancer Hospital, Antenor Duarte Villela, 1331, Barretos, São Paulo, Zip Code: 14784 400, Brazil.ORCID http://orcid.org/0000-0002-9639-7940
Renato José da Silva-OliveiraMolecular Oncology Research Center, Barretos Cancer Hospital, Antenor Duarte Villela, 1331, Barretos, São Paulo, Zip Code: 14784 400, Brazil. renatokjso@gmail.com.ORCID http://orcid.org/0000-0001-6500-4190
Hospital de Câncer de Barretos · BRCentro Universitário da Fundação Educacional de Barretos · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cutaneous squamous cell carcinoma (cSCC) is a common type of skin cancer that can result in significant morbidity, although it is usually well-managed and rarely metastasizes. However, the lack of commercially available cSCC cell lines hinders our understanding of this disease. This study aims to establish and characterize a new metastatic cSCC cell line derived from a Brazilian patient. A tumor biopsy was taken from a metastatic cSCC patient, immortalized, and named HCB-541 after several passages. The cytokeratin expression profile, karyotypic alterations, mutational analysis, mRNA and protein differential expression, tumorigenic capacity in xenograft models, and drug sensitivity were analyzed. The HCB-541 cell line showed a doubling time between 20 and 30 h and high tumorigenic capacity in the xenograft mouse model. The HCB-541 cell line showed hypodiploid and hypotetraploidy populations. We found pathogenic mutations in TP53 p.(Arg248Leu), HRAS (Gln61His) and TERT promoter (C228T) and high-level microsatellite instability (MSI-H) in both tumor and cell line. We observed 37 cancer-related genes differentially expressed when compared with HACAT control cells. The HCB-541 cells exhibited high phosphorylated levels of EGFR, AXL, Tie, FGFR, and ROR2, and high sensitivity to cisplatin, carboplatin, and EGFR inhibitors. Our study successfully established HCB-541, a new cSCC cell line that could be useful as a valuable biological model for understanding the biology and therapy of metastatic skin cancer.

Indexed as

Carcinoma, Squamous CellMutationSkin NeoplasmsAnimalsCell Line, TumorHumansMiceProto-Oncogene Proteins p21(ras)TelomeraseTumor Suppressor Protein p53HRAS protein, humanProto-Oncogene Proteins p21(ras)TelomeraseTERT protein, humanTP53 protein, humanTumor Suppressor Protein p53Cell line establishmentCutaneous squamous cell carcinomaIn vivo modelMolecular profile

Identifiers

PMID38565739
PMCPMC11194207
OpenAlexW4393867945

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.