Survivin, sonic hedgehog, krüppel-like factors, and p53 pathway in serous ovarian cancer: an immunohistochemical study.


Journal

Human pathology
ISSN: 1532-8392
Titre abrégé: Hum Pathol
Pays: United States
ID NLM: 9421547

Informations de publication

Date de publication:
09 2022
Historique:
received: 19 04 2022
revised: 22 06 2022
accepted: 22 06 2022
pubmed: 2 7 2022
medline: 21 9 2022
entrez: 1 7 2022
Statut: ppublish

Résumé

Survivin was previously associated with tumor stage and grade in ovarian cancer and interfered with the tumor's drug sensitivity. In addition, Survivin expression was found to be regulated by the Sonic hedgehog (Shh) pathway, Krüppel-like factor (KLF) family proteins, and p53 pathway. The main aim of this study was to assess the prognostic values of immunohistochemical expression of Survivin, Klf5, Klf11, Shh, p53, p21, and Mdm2 in a cohort of high-grade ovarian serous cancers. Other aims were comparison between high- and low-grade ovarian serous cancer and between platinum-resistant and the other cases. The last aim was to assess the correlations among the immunohistochemical expression of the studied proteins. Retrospective cohort study to assess immunohistochemical expression of Survivin, Klf5, Klf11, Shh, p53, p21, and Mdm2 in a tissue microarray of primary tumor samples among 73 women affected by high-grade ovarian serous cancer and 9 by low-grade ovarian serous cancer. Klf5 and Shh cytoplasmic staining were associated with short overall survival (HR 6.38, 95% CI 2.25-18.01, P < .05 and 2.25, 95% CI 1.19-4.23, P < .05, respectively). In addition, cytoplasmic Klf5 staining, high Klf11, and p53 nuclear staining were associated with platinum resistance (P < .05). Cytoplasmic Shh score was significantly correlated to the immunohistochemical expression of Klf5, Klf11, Mdm2, and Survivin. Our data highlight the possible role of Klf5 and Shh as prognostic markers, meanwhile confirming the role of the KLF family proteins and p53 in ovarian cancer drug resistance. Moreover, Shh appeared to play an important role in the intracellular network of ovarian neoplasia.

Identifiants

pubmed: 35777700
pii: S0046-8177(22)00168-X
doi: 10.1016/j.humpath.2022.06.023
pii:
doi:

Substances chimiques

Biomarkers, Tumor 0
Hedgehog Proteins 0
Kruppel-Like Transcription Factors 0
Survivin 0
Tumor Suppressor Protein p53 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

92-101

Informations de copyright

Copyright © 2022 Elsevier Inc. All rights reserved.

Auteurs

Ambrogio P Londero (AP)

Academic Unit of Obstetrics and Gynaecology; Department of Neuroscience, Rehabilitation, Ophthalmology, Genetics, Maternal and Infant Health, University of Genoa, Genova 16132, Italy; Ennergi Research (non-profit organization), 33050 Lestizza UD, Italy. Electronic address: ambrogio.londero@gmail.com.

Maria Orsaria (M)

Institute of Pathology, DAME, University Hospital of Udine, 33100 Udine UD, Italy.

Luigi Viola (L)

Department of Radiology & Radiotherapy, University of Campania "Luigi Vanvitelli", 80100 Naples, Italy.

Stefania Marzinotto (S)

Institute of Pathology, DAME, University Hospital of Udine, 33100 Udine UD, Italy.

Serena Bertozzi (S)

Ennergi Research (non-profit organization), 33050 Lestizza UD, Italy; Breast Unit, DAME, University Hospital of Udine, 33100 Udine UD, Italy.

Elena Galvano (E)

Lombardi Comprehensive Cancer Center (LCCC), Georgetown University, Washington, DC 20057, USA.

Claudia Andreetta (C)

Oncology Department, University Hospital of Udine, 33100 Udine UD, Italy.

Laura Mariuzzi (L)

Institute of Pathology, DAME, University Hospital of Udine, 33100 Udine UD, Italy.

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Classifications MeSH