The expression and prognostic value of stem cell markers Bmi-1, HESC5:3, and HES77 in human papillomavirus-positive and -negative oropharyngeal squamous cell carcinoma.


Journal

Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine
ISSN: 1423-0380
Titre abrégé: Tumour Biol
Pays: Netherlands
ID NLM: 8409922

Informations de publication

Date de publication:
Mar 2019
Historique:
entrez: 28 3 2019
pubmed: 28 3 2019
medline: 4 4 2019
Statut: ppublish

Résumé

Human papillomavirus is detected in over 50% of oropharyngeal squamous cell carcinomas. Human papillomavirus-positive oropharyngeal squamous cell carcinomas differ from human papillomavirus-negative tumors, and both expression patterns are classified as distinct entities. The Bmi-1 oncogene is a well-known member of the mammalian polycomb-group family. HESC5:3 and HES77 are newly developed monoclonal antibodies produced against undifferentiated embryonic stem cells. Our aim was to explore their roles in both human papillomavirus-positive and -negative oropharyngeal squamous cell carcinomas. Our cohort comprised 202 consecutive oropharyngeal squamous cell carcinoma patients diagnosed and treated with curative intent. We used tissue microarray tumor blocks to study the immunohistochemical expression of Bmi-1, HESC5:3, and HES77. We compared the expressions of these stem cell markers with p16 immunoexpression and human papillomavirus status, as well as with other characteristics of the tumor, and with patients' clinical data and follow-up data. Human papillomavirus- and p16-positive tumors expressed less Bmi-1 and more HESC5:3 than the negative tumors. HES77 expression was high in human papillomavirus-positive oropharyngeal squamous cell carcinoma, but it did not correlate with p16 positivity. In our multivariable model, Bmi-1 and HESC5:3 were still associated with human papillomavirus, but the association between human papillomavirus and HES77 remained absent. In conclusion, Bmi-1, HESC5:3, and HES77 may have a different role in human papillomavirus-positive and human papillomavirus-negative tumors. There was no correlation between Bmi-1, HESC5:3, and HES77 expression and survival.

Identifiants

pubmed: 30915904
doi: 10.1177/1010428319840473
doi:

Substances chimiques

Antibodies, Monoclonal 0
BMI1 protein, human 0
Cyclin-Dependent Kinase Inhibitor Proteins 0
Polycomb Repressive Complex 1 EC 2.3.2.27

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1010428319840473

Auteurs

Hesham Mohamed (H)

1 Department of Pathology, Helsinki University Hospital, University of Helsinki, Helsinki, Finland.
2 Department of Histology, Omar Al-Mukhtar University, El-Beida, Libya.

Jaana Hagström (J)

1 Department of Pathology, Helsinki University Hospital, University of Helsinki, Helsinki, Finland.
3 Translational Cancer Medicine Research Program, Faculty of Medicine, University of Helsinki, Helsinki, Finland.

Lauri Jouhi (L)

4 Department of Otorhinolaryngology-Head and Neck Surgery, Helsinki University Hospital and University of Helsinki, Helsinki, Finland.

Timo Atula (T)

4 Department of Otorhinolaryngology-Head and Neck Surgery, Helsinki University Hospital and University of Helsinki, Helsinki, Finland.

Alhadi Almangush (A)

1 Department of Pathology, Helsinki University Hospital, University of Helsinki, Helsinki, Finland.

Antti Mäkitie (A)

4 Department of Otorhinolaryngology-Head and Neck Surgery, Helsinki University Hospital and University of Helsinki, Helsinki, Finland.
5 Division of Ear, Nose and Throat Diseases, Department of Clinical Sciences, Intervention and Technology and Karolinska University Hospital, Karolinska Institutet, Stockholm, Sweden.
6 Research Programme in Systems Oncology, Faculty of Medicine, University of Helsinki, Helsinki, Finland.

Caj Haglund (C)

3 Translational Cancer Medicine Research Program, Faculty of Medicine, University of Helsinki, Helsinki, Finland.
7 Department of Surgery, Helsinki University Hospital and University of Helsinki, Helsinki, Finland.

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Classifications MeSH